Name

Aniridia, cerebellar ataxia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aniridia, cerebellar ataxia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aniridia cerebellar ataxia mental deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aniridia cerebellar ataxia mental deficiency from the curated CTD Gene-Disease Associations dataset.

Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 from the curated CTD Gene-Disease Associations dataset.

Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 from the curated CTD Gene-Disease Associations dataset.

?cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome from the curated CTD Gene-Disease Associations dataset.

wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebellar ataxia, nonprogressive, with mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebellar ataxia, nonprogressive, with mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset.

mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance from the curated CTD Gene-Disease Associations dataset.

cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated OMIM Gene-Disease Associations dataset.

growth retardation with deafness and mental retardation due to igf1 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the growth retardation with deafness and mental retardation due to igf1 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

Coloboma, uveal, with cleft lip and palate and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Coloboma, uveal, with cleft lip and palate and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations phenotype from the curated OMIM Gene-Disease Associations dataset.

Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia and hypogonadotropic hypogonadism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia and hypogonadotropic hypogonadism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, deafness, and narcolepsy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, deafness, and narcolepsy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

cerebellar ataxia and hypogonadotropic hypogonadism Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebellar ataxia and hypogonadotropic hypogonadism phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebellar ataxia, deafness, and narcolepsy, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebellar ataxia, deafness, and narcolepsy, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

Arthrogryposis, mental retardation, and seizures Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Arthrogryposis, mental retardation, and seizures phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ichthyosis, spastic quadriplegia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ichthyosis, spastic quadriplegia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation with language impairment and autistic features Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation with language impairment and autistic features phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, anterior maxillary protrusion, and strabismus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, anterior maxillary protrusion, and strabismus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypertelorism, severe, with midface prominence, myopia, mental retardation, and bone fragility phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly with mental retardation and digital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly with mental retardation and digital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Iris coloboma with ptosis, hypertelorism, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Iris coloboma with ptosis, hypertelorism, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked rolandic epilepsy with mental retardation and speech dyspraxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked rolandic epilepsy with mental retardation and speech dyspraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal tubular acidosis, proximal, with ocular abnormalities and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alacrima, achalasia, and mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alacrima, achalasia, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Skeletal defects, genital hypoplasia, and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth deficiency and mental retardation with facial dysmorphism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth deficiency and mental retardation with facial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation with short stature, hypogonadism and abnormal gait Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation with short stature, hypogonadism and abnormal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS from the curated CTD Gene-Disease Associations dataset.

Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corpus Callosum, Agenesis of, with Mental Retardation, Ocular Coloboma, and Micrognathia from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Skeletal Dysplasia, and Abducens Palsy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Skeletal Dysplasia, and Abducens Palsy from the curated CTD Gene-Disease Associations dataset.

Scaphocephaly, Maxillary Retrusion, And Mental Retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Scaphocephaly, Maxillary Retrusion, And Mental Retardation from the curated CTD Gene-Disease Associations dataset.

Skeletal Defects, Genital Hypoplasia, And Mental Retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Skeletal Defects, Genital Hypoplasia, And Mental Retardation from the curated CTD Gene-Disease Associations dataset.

Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation from the curated CTD Gene-Disease Associations dataset.

PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS from the curated CTD Gene-Disease Associations dataset.

Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis from the curated CTD Gene-Disease Associations dataset.

Cleft Palate, Isolated, And Mental Retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cleft Palate, Isolated, And Mental Retardation from the curated CTD Gene-Disease Associations dataset.

Microcephaly with Mental Retardation and Digital Anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microcephaly with Mental Retardation and Digital Anomalies from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Severe, With Spasticity And Pigmentary Tapetoretinal Degeneration Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Severe, With Spasticity And Pigmentary Tapetoretinal Degeneration from the curated CTD Gene-Disease Associations dataset.

Cubitus Valgus with Mental Retardation and Unusual Facies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cubitus Valgus with Mental Retardation and Unusual Facies from the curated CTD Gene-Disease Associations dataset.

Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked from the curated CTD Gene-Disease Associations dataset.

epilepsy and mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy and mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mental retardation, severe, with spasticity and tapetoretinal degeneration Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, severe, with spasticity and tapetoretinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation with language impairment and autistic features Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation with language impairment and autistic features phenotype from the curated OMIM Gene-Disease Associations dataset.

?rolandic epilepsy, mental retardation, and speech dyspraxia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?rolandic epilepsy, mental retardation, and speech dyspraxia phenotype from the curated OMIM Gene-Disease Associations dataset.

skeletal defects, genital hypoplasia, and mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the skeletal defects, genital hypoplasia, and mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, anterior maxillary protrusion, and strabismus Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, anterior maxillary protrusion, and strabismus phenotype from the curated OMIM Gene-Disease Associations dataset.

corpus callosum, agenesis of, with mental retardation, ocular coloboma and micrognathia Gene Set

From OMIM Gene-Disease Associations

genes associated with the corpus callosum, agenesis of, with mental retardation, ocular coloboma and micrognathia phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, truncal obesity, retinal dystrophy, and micropenis Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, truncal obesity, retinal dystrophy, and micropenis phenotype from the curated OMIM Gene-Disease Associations dataset.

alacrima, achalasia, and mental retardation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the alacrima, achalasia, and mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

?arthrogryposis, mental retardation, and seizures Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?arthrogryposis, mental retardation, and seizures phenotype from the curated OMIM Gene-Disease Associations dataset.

choroideremia, deafness, and mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the choroideremia, deafness, and mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

scaphocephaly, maxillary retrusion, and mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the scaphocephaly, maxillary retrusion, and mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations phenotype from the curated OMIM Gene-Disease Associations dataset.

cubitus valgus with mental retardation and unusual facies Gene Set

From OMIM Gene-Disease Associations

genes associated with the cubitus valgus with mental retardation and unusual facies phenotype from the curated OMIM Gene-Disease Associations dataset.

epilepsy, focal, with speech disorder and with or without mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the epilepsy, focal, with speech disorder and with or without mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 29 and others Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 29 and others phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, spastic quadriplegia, and mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, spastic quadriplegia, and mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 3 (methylmalonic acidemia and homocysteinemia, cblx type ) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 3 (methylmalonic acidemia and homocysteinemia, cblx type ) phenotype from the curated OMIM Gene-Disease Associations dataset.

coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis phenotype from the curated OMIM Gene-Disease Associations dataset.

Cognitive impairment with or without cerebellar ataxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cognitive impairment with or without cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia infantile with progressive external ophthalmoplegia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia infantile with progressive external ophthalmoplegia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar Ataxia, Cayman Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebellar Ataxia, Cayman Type from the curated CTD Gene-Disease Associations dataset.

Cerebellar Ataxia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebellar Ataxia from the curated CTD Gene-Disease Associations dataset.

cerebellar ataxia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease cerebellar ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

cerebellar ataxia; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebellar ataxia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebellar ataxia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebellar ataxia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

nonprogressive cerebellar ataxia Gene Set

From HPO Gene-Disease Associations

genes associated with the nonprogressive cerebellar ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

progressive cerebellar ataxia Gene Set

From HPO Gene-Disease Associations

genes associated with the progressive cerebellar ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Cerebellar Ataxia Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Cerebellar Ataxia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

cognitive impairment with or without cerebellar ataxia Gene Set

From OMIM Gene-Disease Associations

genes associated with the cognitive impairment with or without cerebellar ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.

ataxia, cerebellar, cayman type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ataxia, cerebellar, cayman type phenotype from the curated OMIM Gene-Disease Associations dataset.

migraine, familial hemiplegic, 1, with progressive cerebellar ataxia Gene Set

From OMIM Gene-Disease Associations

genes associated with the migraine, familial hemiplegic, 1, with progressive cerebellar ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebellar ataxia Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebellar ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.

Congenital aniridia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital aniridia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aniridia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aniridia from the curated CTD Gene-Disease Associations dataset.

Aniridia, type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aniridia, type 2 from the curated CTD Gene-Disease Associations dataset.

aniridia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease aniridia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

aniridia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease aniridia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

aniridia Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term aniridia in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

aniridia Gene Set

From HPO Gene-Disease Associations

genes associated with the aniridia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aniridia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the aniridia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

?aniridia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?aniridia phenotype from the curated OMIM Gene-Disease Associations dataset.

aniridia Gene Set

From OMIM Gene-Disease Associations

genes associated with the aniridia phenotype from the curated OMIM Gene-Disease Associations dataset.

Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset.

X-linked mental retardation 58 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation 58 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked 45 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 45 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation, syndromic, Claes-Jensen type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation, syndromic, Claes-Jensen type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation 63 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation 63 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, syndromic, turner type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, syndromic, turner type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 30 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 30 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 24 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 24 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 28 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 28 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-Linked mental retardation 90 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-Linked mental retardation 90 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation X-linked syndromic 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation X-linked syndromic 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 23 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 23 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 27 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 27 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 29 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 29 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Syndromic X-linked mental retardation 16 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Syndromic X-linked mental retardation 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Siderius X-linked mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Siderius X-linked mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation with marfanoid habitus syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation with marfanoid habitus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Wilson-Turner X-linked mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Wilson-Turner X-linked mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, syndromic, raymond type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, syndromic, raymond type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation, syndromic 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation, syndromic 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Birk Barel mental retardation dysmorphism syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Birk Barel mental retardation dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperphosphatasia with mental retardation syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperphosphatasia with mental retardation syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperphosphatasia with mental retardation syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperphosphatasia with mental retardation syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperphosphatasia with mental retardation syndrome 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperphosphatasia with mental retardation syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperphosphatasia with mental retardation syndrome 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperphosphatasia with mental retardation syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperphosphatasia with mental retardation syndrome 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperphosphatasia with mental retardation syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked 19 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ZNF711-Related X-linked Mental Retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the ZNF711-Related X-linked Mental Retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 27 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 27 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation, with or without seizures, ARX-related Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation, with or without seizures, ARX-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 39 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 39 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Focal epilepsy with speech disorder with or without mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Focal epilepsy with speech disorder with or without mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 38 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 38 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 34 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 34 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, syndromic 32 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, syndromic 32 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, syndromic, wu type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, syndromic, wu type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-Linked Mental Retardation 41 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-Linked Mental Retardation 41 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, syndromic, Hedera type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, syndromic, Hedera type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked syndromic mental retardation, Nascimento type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked syndromic mental retardation, Nascimento type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 47 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 47 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation 21 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation 21 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, nonspecific Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, nonspecific phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation 30 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation 30 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked, syndromic 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked, syndromic 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 19 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 40 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 40 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 41 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 41 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 42 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 42 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 43 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 43 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 44 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 44 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 45 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 45 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal recessive 46 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal recessive 46 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked 93 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 93 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked 96 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 96 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked 98 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 98 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked 99 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 99 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, X-linked 72 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, X-linked 72 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 15 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, autosomal dominant 17 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, autosomal dominant 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Siderius X-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Siderius X-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.

Partington X-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Partington X-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.

Alopecia-Mental Retardation Syndrome 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alopecia-Mental Retardation Syndrome 1 from the curated CTD Gene-Disease Associations dataset.

Alopecia-Mental Retardation Syndrome 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alopecia-Mental Retardation Syndrome 2 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 30 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 30 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Recessive 13 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 13 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 23 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 23 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 91 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 91 from the curated CTD Gene-Disease Associations dataset.

Miles-Carpenter x-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Miles-Carpenter x-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 95 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 95 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 9 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 77 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 77 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic 13 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic 13 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic 12 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic 14 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic 14 from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, X-LINKED, SYNDROMIC, RAYMOND TYPE from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 3 from the curated CTD Gene-Disease Associations dataset.

Lubs X-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lubs X-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Fra12a Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Fra12a Type from the curated CTD Gene-Disease Associations dataset.

HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, with Short Stature Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, with Short Stature from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 20 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 20 from the curated CTD Gene-Disease Associations dataset.

Mental retardation X-linked syndromic 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental retardation X-linked syndromic 7 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Dominant 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Dominant 3 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Dominant 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Dominant 5 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Dominant 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Dominant 4 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 17 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 17 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic, Jarid1c-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic, Jarid1c-Related from the curated CTD Gene-Disease Associations dataset.

X-linked mental retardation Gustavson type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease X-linked mental retardation Gustavson type from the curated CTD Gene-Disease Associations dataset.

Epilepsy, Female-Restricted, with Mental Retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, Female-Restricted, with Mental Retardation from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 81 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 81 from the curated CTD Gene-Disease Associations dataset.

Mental retardation, X-linked 14 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental retardation, X-linked 14 from the curated CTD Gene-Disease Associations dataset.

Alpha-Thalassemia Mental Retardation Syndrome, Deletion-Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alpha-Thalassemia Mental Retardation Syndrome, Deletion-Type from the curated CTD Gene-Disease Associations dataset.

Mental retardation-hypotonic facies syndrome, x-linked, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental retardation-hypotonic facies syndrome, x-linked, 1 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic, Christianson Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic, Christianson Type from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 84 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 84 from the curated CTD Gene-Disease Associations dataset.

Mental retardation, X-linked, syndromic 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental retardation, X-linked, syndromic 5 from the curated CTD Gene-Disease Associations dataset.

BRACHYDACTYLY-MENTAL RETARDATION SYNDROME Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BRACHYDACTYLY-MENTAL RETARDATION SYNDROME from the curated CTD Gene-Disease Associations dataset.

Birk-Barel Mental Retardation Dysmorphism Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Birk-Barel Mental Retardation Dysmorphism Syndrome from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 from the curated CTD Gene-Disease Associations dataset.

MASA (Mental Retardation, Aphasia, Shuffling Gait, Adducted Thumbs) Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MASA (Mental Retardation, Aphasia, Shuffling Gait, Adducted Thumbs) Syndrome from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, X-LINKED 21 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, X-LINKED 21 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, with Epilepsy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, with Epilepsy from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Recessive 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 9 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 78 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 78 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Recessive 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 3 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 1 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 73 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 73 from the curated CTD Gene-Disease Associations dataset.

Abidi X-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Abidi X-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Recessive 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 4 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 82 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 82 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Recessive 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 11 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Recessive 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 10 from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, X-LINKED 96 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, X-LINKED 96 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Recessive 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 8 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Recessive 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 2 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Recessive 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 7 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Recessive 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 6 from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, X-LINKED 49 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, X-LINKED 49 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, With Panhypopituitarism Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, With Panhypopituitarism from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, With Or Without Seizures, Arx-Related from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 52 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 52 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 53 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 53 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 58 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 58 from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, AUTOSOMAL DOMINANT 20 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, AUTOSOMAL DOMINANT 20 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Recessive 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Recessive 1 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 63 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 63 from the curated CTD Gene-Disease Associations dataset.

Armfield X-Linked Mental Retardation Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Armfield X-Linked Mental Retardation Syndrome from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 42 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 42 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 93 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 93 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 94 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 94 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOUT MENTAL RETARDATION), TYPE B, 4 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic, Turner Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic, Turner Type from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 2 from the curated CTD Gene-Disease Associations dataset.

MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, X-LINKED, SYNDROMIC, CABEZAS TYPE from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 72 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 72 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 45 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 45 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 46 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 46 from the curated CTD Gene-Disease Associations dataset.

Prieto X-linked mental retardation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Prieto X-linked mental retardation syndrome from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked, Syndromic 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, Syndromic 10 from the curated CTD Gene-Disease Associations dataset.

Martin-Probst Deafness-Mental Retardation Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Martin-Probst Deafness-Mental Retardation Syndrome from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, X-Linked 50 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked 50 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, Autosomal Dominant 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, Autosomal Dominant 1 from the curated CTD Gene-Disease Associations dataset.

Parkinsonism, early onset with mental retardation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinsonism, early onset with mental retardation from the curated CTD Gene-Disease Associations dataset.

non-specific x-linked mental retardation Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease non-specific x-linked mental retardation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

epilepsy; mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mental retardation; rett syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mental retardation; rett syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; craniofacial abnormalities; mental retardation; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; craniofacial abnormalities; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

language development disorders; mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease language development disorders; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fragile x syndrome; mental retardation; spinocerebellar degenerations; tremor Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fragile x syndrome; mental retardation; spinocerebellar degenerations; tremor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fragile x syndrome; fragile x syndromes; mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fragile x syndrome; fragile x syndromes; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mental retardation; muscular dystrophy, duchenne Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mental retardation; muscular dystrophy, duchenne in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

violent offenders with mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease violent offenders with mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

schizophrenia; mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease schizophrenia; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukomalacia, periventricular; mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukomalacia, periventricular; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mental retardation; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

non-syndromic x-linked mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease non-syndromic x-linked mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain diseases; mental retardation, x-linked Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain diseases; mental retardation, x-linked in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital abnormalities; mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital abnormalities; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

learning disorders; memory disorders; mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease learning disorders; memory disorders; mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

x-linked mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease x-linked mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mental retardation, x-linked Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mental retardation, x-linked in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mental retardation, x-linked; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mental retardation, x-linked; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mental retardation; microcephaly Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mental retardation; microcephaly in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mental retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mental retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Mental Retardation, X-Linked Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Mental Retardation, X-Linked phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Mental Retardation Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Mental Retardation phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Nuclear fragile X mental retardation-interacting protein 1, conserved domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Nuclear fragile X mental retardation-interacting protein 1, conserved domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Fragile X mental retardation protein family Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Fragile X mental retardation protein family protein domain from the InterPro Predicted Protein Domain Annotations dataset.

mental retardation, autosomal recessive, 9/26 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive, 9/26 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 19 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 19 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 18 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 18 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 15 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 15 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 17 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 16 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 16 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 84 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 84 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 81 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 81 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 82 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 82 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 89 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 89 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 28 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 28 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 29 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 29 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 23 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 23 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 27 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 27 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 24 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 24 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 25 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 25 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 30 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 30 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, snyder-robinson type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, snyder-robinson type phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 30/47 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 30/47 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, x-linked syndromic 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, x-linked syndromic 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation syndrome, x-linked, siderius type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation syndrome, x-linked, siderius type phenotype from the curated OMIM Gene-Disease Associations dataset.

alpha-thalassemia/mental retardation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the alpha-thalassemia/mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic 16 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic 16 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 40 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 40 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 44 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 44 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 46 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 46 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, fraxe type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, fraxe type phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation syndrome, x-linked, armfield type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation syndrome, x-linked, armfield type phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, x-linked, syndromic 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, x-linked, syndromic 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperphosphatasia with mental retardation syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperphosphatasia with mental retardation syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperphosphatasia with mental retardation syndrome 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperphosphatasia with mental retardation syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperphosphatasia with mental retardation syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperphosphatasia with mental retardation syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperphosphatasia with mental retardation syndrome 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperphosphatasia with mental retardation syndrome 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, with isolated growth hormone deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, with isolated growth hormone deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, x-linked, syndromic, hedera type Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, x-linked, syndromic, hedera type phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, x-linked 91 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, x-linked 91 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 90 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 90 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 98 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 98 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 32 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 32 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic, shashi type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic, shashi type phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation-hypotonic facies syndrome, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation-hypotonic facies syndrome, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type b, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive, 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, autosomal dominant 22 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, autosomal dominant 22 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 30 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 30 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 78 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 78 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 72 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 72 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic 32 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic 32 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 52 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 52 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 53 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 53 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 50 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 50 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 58 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 58 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic, claes-jensen type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic, claes-jensen type phenotype from the curated OMIM Gene-Disease Associations dataset.

waisman parkinsonism-mental retardation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the waisman parkinsonism-mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic, nascimento-type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic, nascimento-type phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 21/34 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 21/34 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 31 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 31 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic 17 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 10/20 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 10/20 phenotype from the curated OMIM Gene-Disease Associations dataset.

?stocco dos santos x-linked mental retardation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?stocco dos santos x-linked mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 19 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 19 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

birk-barel mental retardation dysmorphism syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the birk-barel mental retardation dysmorphism syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 77 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 77 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic 15 (cabezas type) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic 15 (cabezas type) phenotype from the curated OMIM Gene-Disease Associations dataset.

brachydactyly-mental retardation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the brachydactyly-mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, with short stature Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, with short stature phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, autosomal recessive 45 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, autosomal recessive 45 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, autosomal recessive 42 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, autosomal recessive 42 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, autosomal recessive 43 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, autosomal recessive 43 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, syndromic, chudley-schwartz type, Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, syndromic, chudley-schwartz type, phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 92 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 92 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 93 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 93 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 96 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 96 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 97 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 97 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 94 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 94 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 95 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 95 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 99 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 99 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 39 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 39 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 38 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 38 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 31 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 31 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 33 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 33 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 35 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 35 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 34 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 34 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 36 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 36 phenotype from the curated OMIM Gene-Disease Associations dataset.

alopecia-mental retardation syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the alopecia-mental retardation syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

alopecia-mental retardation syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the alopecia-mental retardation syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

alopecia-mental retardation syndrome 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the alopecia-mental retardation syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 21 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 21 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 23 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 23 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 24 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 24 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 26 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 26 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant 29 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant 29 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation-skeletal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation-skeletal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 16 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 16 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 15 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 15 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 19 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 19 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 18 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 18 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic, raymond type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic, raymond type phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic, abidi type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic, abidi type phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly with or without chorioretinopathy, lymphedema, or mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly with or without chorioretinopathy, lymphedema, or mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, with or without nystagmus Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, with or without nystagmus phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

alpha-thalassemia/mental retardation syndrome, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the alpha-thalassemia/mental retardation syndrome, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

?hyperphosphatasia with mental retardation syndrome 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?hyperphosphatasia with mental retardation syndrome 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 41 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 41 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 63 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 63 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive, 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, x-linked 101 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, x-linked 101 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, x-linked 100 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, x-linked 100 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic, turner type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic, turner type phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 49 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 49 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 41 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 41 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 42 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 42 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 45 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 45 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 46 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 46 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic, lubs type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic, lubs type phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, autosomal dominant 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, autosomal dominant 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 23 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 23 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked 20 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked 20 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type b, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal recessive 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal recessive 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant, 27 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant, 27 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type b, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, fra12a type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, fra12a type phenotype from the curated OMIM Gene-Disease Associations dataset.

megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the megalencephalic leukoencephalopathy with subcortical cysts 2b, remitting, with or without mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, autosomal recessive, 37 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, autosomal recessive, 37 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, autosomal dominant, 28 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, autosomal dominant, 28 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked syndromic, christianson type Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked syndromic, christianson type phenotype from the curated OMIM Gene-Disease Associations dataset.

birth weight; fetal growth retardation; intrauterine growth retardation; vitamin d deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; fetal growth retardation; intrauterine growth retardation; vitamin d deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; placenta diseases; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; placenta diseases; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abruptio placentae; congenital abnormalities; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abruptio placentae; congenital abnormalities; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, habitual; activated protein c resistance; fetal growth retardation; hypertension; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; activated protein c resistance; fetal growth retardation; hypertension; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abruptio placentae; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abruptio placentae; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal growth retardation; hellp syndrome; intrauterine growth retardation; pregnancy complications, hematologic; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal growth retardation; hellp syndrome; intrauterine growth retardation; pregnancy complications, hematologic; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal growth retardation; intrauterine growth retardation; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal growth retardation; intrauterine growth retardation; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, spontaneous; abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, spontaneous; abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal growth retardation; infant, premature, diseases; intrauterine growth retardation; sepsis; systemic infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal growth retardation; infant, premature, diseases; intrauterine growth retardation; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal diseases; fetal growth retardation; hypertension induced by pregnancy; hypertension, pregnancy-induced; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal diseases; fetal growth retardation; hypertension induced by pregnancy; hypertension, pregnancy-induced; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, spontaneous; activated protein c resistance; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, spontaneous; activated protein c resistance; fetal growth retardation; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abruptio placentae; fetal death; fetal growth retardation; intrauterine growth retardation; placenta abruptio; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal growth retardation; hellp syndrome; intrauterine growth retardation; pre-eclampsia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal growth retardation; hellp syndrome; intrauterine growth retardation; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal growth retardation; intrauterine growth retardation; pre-eclampsia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal growth retardation; intrauterine growth retardation; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal growth retardation; intrauterine growth retardation; pregnancy complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal growth retardation; intrauterine growth retardation; pregnancy complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal growth retardation; intrauterine growth retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal growth retardation; intrauterine growth retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; fetal growth retardation; intrauterine growth retardation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; fetal growth retardation; intrauterine growth retardation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebellar medulloblastomas and cutaneous basal cell carcinomas. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebellar medulloblastomas and cutaneous basal cell carcinomas. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pancreatic and cerebellar agenesis Gene Set

From OMIM Gene-Disease Associations

genes associated with the pancreatic and cerebellar agenesis phenotype from the curated OMIM Gene-Disease Associations dataset.

Anemia sideroblastic and spinocerebellar ataxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Anemia sideroblastic and spinocerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract from the curated CTD Gene-Disease Associations dataset.

Early-onset ataxia with oculomotor apraxia and hypoalbuminemia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Early-onset ataxia with oculomotor apraxia and hypoalbuminemia from the curated CTD Gene-Disease Associations dataset.

polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene Set

From OMIM Gene-Disease Associations

genes associated with the polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial recessive ataxia syndrome (includes sando and scae) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial recessive ataxia syndrome (includes sando and scae) phenotype from the curated OMIM Gene-Disease Associations dataset.

ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia phenotype from the curated OMIM Gene-Disease Associations dataset.

Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Set

From Reactome Pathways

proteins participating in the Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways dataset.

Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth retardation, developmental delay, coarse facies, and early death Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth retardation, developmental delay, coarse facies, and early death phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Psychomotor retardation, epilepsy, and craniofacial dysmorphism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Psychomotor retardation, epilepsy, and craniofacial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation from the curated CTD Gene-Disease Associations dataset.

Growth Retardation, Developmental Delay, Coarse Facies, And Early Death Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Growth Retardation, Developmental Delay, Coarse Facies, And Early Death from the curated CTD Gene-Disease Associations dataset.

psychomotor retardation, epilepsy, and craniofacial dysmorphism Gene Set

From OMIM Gene-Disease Associations

genes associated with the psychomotor retardation, epilepsy, and craniofacial dysmorphism phenotype from the curated OMIM Gene-Disease Associations dataset.

severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene Set

From OMIM Gene-Disease Associations

genes associated with the severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation phenotype from the curated OMIM Gene-Disease Associations dataset.

growth retardation, developmental delay, coarse facies, and early death Gene Set

From OMIM Gene-Disease Associations

genes associated with the growth retardation, developmental delay, coarse facies, and early death phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebellar hemisphere Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in cerebellar hemisphere relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

dorsolateral (non-cerebellar) part of isA Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in dorsolateral (non-cerebellar) part of isA relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

mantle zone of cerebellar vermis Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in mantle zone of cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

cerebellar white matter Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in cerebellar white matter relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

white matter of cerebellar vermis Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in white matter of cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

lateral (dentate) cerebellar nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral (dentate) cerebellar nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

cerebellar vermis Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

cerebellar nuclei of CbH Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in cerebellar nuclei of CbH relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Cerebellar nuclei Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Cerebellar nuclei relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

cortex of cerebellar hemisphere Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in cortex of cerebellar hemisphere relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

intermediate (interpositus) cerebellar nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in intermediate (interpositus) cerebellar nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

cortex of cerebellar vermis Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in cortex of cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

superficial stratum of cerebellar vermis Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in superficial stratum of cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

medial (fastigial) cerebellar nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in medial (fastigial) cerebellar nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

cerebellar nuclei of CbV Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in cerebellar nuclei of CbV relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

superficial stratum of cerebellar hemisphere Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in superficial stratum of cerebellar hemisphere relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

intermediate stratum of cerebellar vermis Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in intermediate stratum of cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Cerebellar cortex Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Cerebellar cortex relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

periventricular stratum of cerebellar vermis Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in periventricular stratum of cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

cerebellar cortex_24 pcw_M_12288 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in cerebellar cortex_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

cerebellar cortex_3 yrs_F_12836 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in cerebellar cortex_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

cerebellar cortex_4 mos_M_12296 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in cerebellar cortex_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

cerebellar cortex_2 yrs_F_12979 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in cerebellar cortex_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

cerebellar cortex_23 yrs_M_12300 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in cerebellar cortex_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

cerebellar cortex_21 pcw_F_12365 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in cerebellar cortex_21 pcw_F_12365 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

cerebellar cortex_30 yrs_F_12290 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in cerebellar cortex_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

cerebellar cortex_13 yrs_F_12831 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in cerebellar cortex_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

cerebellar cortex_8 yrs_M_12841 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in cerebellar cortex_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

cerebellar cortex_21 pcw_M_12886 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in cerebellar cortex_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

cerebellar cortex_3 yrs_M_12980 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in cerebellar cortex_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

cerebellar cortex_18 yrs_M_12984 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in cerebellar cortex_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

cerebellar cortex_15 yrs_M_12299 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in cerebellar cortex_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

cerebellar cortex_4 yrs_M_12298 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in cerebellar cortex_4 yrs_M_12298 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

cerebellar cortex_1 yrs_F_12830 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in cerebellar cortex_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

cerebellar cortex_21 yrs_F_13057 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in cerebellar cortex_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

cerebellar cortex_12 pcw_F_13060 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in cerebellar cortex_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

cerebellar cortex_36 yrs_M_12302 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in cerebellar cortex_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

cerebellar cortex_17 pcw_F_12880 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in cerebellar cortex_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

cerebellar cortex_10 mos_M_12977 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in cerebellar cortex_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

cerebellar cortex_26 pcw_F_12949 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in cerebellar cortex_26 pcw_F_12949 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

cerebellar cortex_24 pcw_M_12288 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_11 yrs_F_12289 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_11 yrs_F_12289 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_40 yrs_F_12304 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_3 yrs_F_12836 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_4 mos_M_12296 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_23 yrs_M_12300 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_21 pcw_F_12365 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_21 pcw_F_12365 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_30 yrs_F_12290 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_13 yrs_F_12831 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_2 yrs_F_12979 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_37 yrs_M_12303 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_8 yrs_M_12841 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_17 pcw_F_12880 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_21 pcw_M_12886 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_3 yrs_M_12980 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_18 yrs_M_12984 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_15 yrs_M_12299 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_4 yrs_M_12298 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_4 yrs_M_12298 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_8 yrs_M_12981 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_8 yrs_M_12981 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_4 mos_M_12890 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_4 mos_M_12890 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_1 yrs_F_12830 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_16 pcw_M_12837 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_19 yrs_F_12832 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_19 yrs_F_12832 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_21 yrs_F_13057 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_12 pcw_F_13060 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_37 pcw_M_263195015 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_37 pcw_M_263195015 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_36 yrs_M_12302 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_10 mos_M_12977 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar cortex_35 pcw_F_12295 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in cerebellar cortex_35 pcw_F_12295 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

cerebellar vermis Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in cerebellar vermis relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

Diabetes mellitus, permanent neonatal, with cerebellar agenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diabetes mellitus, permanent neonatal, with cerebellar agenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

cerebellar mossy fiber Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the cerebellar mossy fiber cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

cerebellar mossy fiber Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the cerebellar mossy fiber cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

Diabetes Mellitus, Permanent Neonatal, with Cerebellar Agenesis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Diabetes Mellitus, Permanent Neonatal, with Cerebellar Agenesis from the curated CTD Gene-Disease Associations dataset.

CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 3 from the curated CTD Gene-Disease Associations dataset.

Cerebellar Diseases Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebellar Diseases from the curated CTD Gene-Disease Associations dataset.

cerebellar disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease cerebellar disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

cerebellar disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease cerebellar disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

cerebellar liponeurocytoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease cerebellar liponeurocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

cerebellar medulloblastoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease cerebellar medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

cerebellar astrocytoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease cerebellar astrocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

cerebellar angioblastoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease cerebellar angioblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

myoclonic cerebellar dyssynergia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease myoclonic cerebellar dyssynergia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

primary cerebellar degeneration Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease primary cerebellar degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

huntington disease; myoclonic cerebellar dyssynergia; spinocerebellar ataxias Gene Set

From GAD Gene-Disease Associations

genes associated with the disease huntington disease; myoclonic cerebellar dyssynergia; spinocerebellar ataxias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain neoplasms; cerebellar neoplasms; ganglioglioma; glioma; medulloblastoma; neuroectodermal tumor, primitive; neuroectodermal tumors, primitive Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brain neoplasms; cerebellar neoplasms; ganglioglioma; glioma; medulloblastoma; neuroectodermal tumor, primitive; neuroectodermal tumors, primitive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebellar neoplasms; medulloblastoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebellar neoplasms; medulloblastoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebellar neoplasms; hemangioblastoma; von hippel-lindau disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebellar neoplasms; hemangioblastoma; von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebellar volume Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebellar volume in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adrenal gland neoplasms; carcinoma, renal cell; cerebellar neoplasms; hemangioblastoma; kidney neoplasms; pheochromocytoma; retinal neoplasms; von hippel-lindau disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adrenal gland neoplasms; carcinoma, renal cell; cerebellar neoplasms; hemangioblastoma; kidney neoplasms; pheochromocytoma; retinal neoplasms; von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebellar Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term cerebellar in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

CSTB_KO_GSE47516_18_mouse_brain (P7 cerebellum, P30 cerebellum, cerebellar granule cells) Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the CSTB_KO_GSE47516_18_mouse_brain (P7 cerebellum, P30 cerebellum, cerebellar granule cells) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

regulation of cerebellar granule cell precursor proliferation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cerebellar granule cell precursor proliferation biological process from the curated GO Biological Process Annotations dataset.

cerebellar cortex structural organization Gene Set

From GO Biological Process Annotations

genes participating in the cerebellar cortex structural organization biological process from the curated GO Biological Process Annotations dataset.

cerebellar granular layer development Gene Set

From GO Biological Process Annotations

genes participating in the cerebellar granular layer development biological process from the curated GO Biological Process Annotations dataset.

cerebellar purkinje cell layer morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the cerebellar purkinje cell layer morphogenesis biological process from the curated GO Biological Process Annotations dataset.

cerebellar purkinje cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the cerebellar purkinje cell differentiation biological process from the curated GO Biological Process Annotations dataset.

cerebellar cortex formation Gene Set

From GO Biological Process Annotations

genes participating in the cerebellar cortex formation biological process from the curated GO Biological Process Annotations dataset.

cerebellar cortex morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the cerebellar cortex morphogenesis biological process from the curated GO Biological Process Annotations dataset.

cerebellar granule cell precursor tangential migration Gene Set

From GO Biological Process Annotations

genes participating in the cerebellar granule cell precursor tangential migration biological process from the curated GO Biological Process Annotations dataset.

cerebellar molecular layer development Gene Set

From GO Biological Process Annotations

genes participating in the cerebellar molecular layer development biological process from the curated GO Biological Process Annotations dataset.

cerebellar purkinje cell layer structural organization Gene Set

From GO Biological Process Annotations

genes participating in the cerebellar purkinje cell layer structural organization biological process from the curated GO Biological Process Annotations dataset.

cerebellar purkinje cell layer development Gene Set

From GO Biological Process Annotations

genes participating in the cerebellar purkinje cell layer development biological process from the curated GO Biological Process Annotations dataset.

cerebellar cortex development Gene Set

From GO Biological Process Annotations

genes participating in the cerebellar cortex development biological process from the curated GO Biological Process Annotations dataset.

cerebellar purkinje cell-granule cell precursor cell signaling involved in regulation of granule cell precursor cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the cerebellar purkinje cell-granule cell precursor cell signaling involved in regulation of granule cell precursor cell proliferation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of cerebellar granule cell precursor proliferation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of cerebellar granule cell precursor proliferation biological process from the curated GO Biological Process Annotations dataset.

cerebellar granule cell precursor proliferation Gene Set

From GO Biological Process Annotations

genes participating in the cerebellar granule cell precursor proliferation biological process from the curated GO Biological Process Annotations dataset.

radial glia guided migration of cerebellar granule cell Gene Set

From GO Biological Process Annotations

genes participating in the radial glia guided migration of cerebellar granule cell biological process from the curated GO Biological Process Annotations dataset.

cerebellar granular layer morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the cerebellar granular layer morphogenesis biological process from the curated GO Biological Process Annotations dataset.

smoothened signaling pathway involved in regulation of cerebellar granule cell precursor cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the smoothened signaling pathway involved in regulation of cerebellar granule cell precursor cell proliferation biological process from the curated GO Biological Process Annotations dataset.

positive regulation of cerebellar granule cell precursor proliferation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of cerebellar granule cell precursor proliferation biological process from the curated GO Biological Process Annotations dataset.

cerebellar purkinje cell layer maturation Gene Set

From GO Biological Process Annotations

genes participating in the cerebellar purkinje cell layer maturation biological process from the curated GO Biological Process Annotations dataset.

cerebellar granule cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the cerebellar granule cell differentiation biological process from the curated GO Biological Process Annotations dataset.

cerebellar granular layer structural organization Gene Set

From GO Biological Process Annotations

genes participating in the cerebellar granular layer structural organization biological process from the curated GO Biological Process Annotations dataset.

cerebellar granular layer maturation Gene Set

From GO Biological Process Annotations

genes participating in the cerebellar granular layer maturation biological process from the curated GO Biological Process Annotations dataset.

cerebellar mossy fiber Gene Set

From GO Cellular Component Annotations

proteins localized to the cerebellar mossy fiber cellular component from the curated GO Cellular Component Annotations dataset.

abnormality of the cerebellar peduncle Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the cerebellar peduncle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia of the inferior half of the cerebellar vermis Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia of the inferior half of the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebellar cortical atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebellar cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

thickened superior cerebellar peduncle Gene Set

From HPO Gene-Disease Associations

genes associated with the thickened superior cerebellar peduncle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

agenesis of cerebellar vermis Gene Set

From HPO Gene-Disease Associations

genes associated with the agenesis of cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

diffuse cerebellar atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the diffuse cerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebellar cyst Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebellar cyst phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebellar hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebellar hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia of the cerebellar vermis Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia of the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebellar atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

elongated superior cerebellar peduncle Gene Set

From HPO Gene-Disease Associations

genes associated with the elongated superior cerebellar peduncle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

dysgenesis of the cerebellar vermis Gene Set

From HPO Gene-Disease Associations

genes associated with the dysgenesis of the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebellar vermis atrophy Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebellar vermis atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebellar hemisphere hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebellar hemisphere hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebellar hemorrhage Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebellar hemorrhage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebellar vermis hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebellar vermis hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebellar dysplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebellar dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

disorganization of the anterior cerebellar vermis Gene Set

From HPO Gene-Disease Associations

genes associated with the disorganization of the anterior cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the superior cerebellar peduncle Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the superior cerebellar peduncle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the cerebellar vermis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebellar malformation Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebellar malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebellar calcifications Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebellar calcifications phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cerebellar hemangioblastoma Gene Set

From HPO Gene-Disease Associations

genes associated with the cerebellar hemangioblastoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

loss of purkinje cells in the cerebellar vermis Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of purkinje cells in the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

dense calcifications in the cerebellar dentate nucleus Gene Set

From HPO Gene-Disease Associations

genes associated with the dense calcifications in the cerebellar dentate nucleus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Cerebellar Diseases Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Cerebellar Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Cerebellar Neoplasms Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Cerebellar Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Myoclonic Cerebellar Dyssynergia Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Myoclonic Cerebellar Dyssynergia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Cerebellar degeneration-related protein 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cerebellar degeneration-related protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

thin cerebellar molecular layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin cerebellar molecular layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cerebellar molecular layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cerebellar molecular layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cerebellar lobule formation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cerebellar lobule formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cerebellar hemisphere morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cerebellar hemisphere morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cerebellar purkinje cell layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cerebellar purkinje cell layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased cerebellar granule cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cerebellar granule cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent cerebellar foliation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent cerebellar foliation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent cerebellar granule cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent cerebellar granule cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cerebellar layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cerebellar layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

thin cerebellar granule layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the thin cerebellar granule layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cerebellar granule layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cerebellar granule layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cerebellar golgi cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cerebellar golgi cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cerebellar peduncle morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cerebellar peduncle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

reduced cerebellar foliation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the reduced cerebellar foliation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent cerebellar lobules Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent cerebellar lobules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cerebellar granule cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cerebellar granule cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cerebellar cortex morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cerebellar cortex morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

delaminated cerebellar granule layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the delaminated cerebellar granule layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

ectopic cerebellar granule cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ectopic cerebellar granule cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cerebellar plate morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cerebellar plate morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cerebellar granule cell migration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cerebellar granule cell migration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cerebellar foliation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cerebellar foliation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent cerebellar granule layer Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent cerebellar granule layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cerebellar granule cell proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cerebellar granule cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

hemangioblastoma, cerebellar, somatic Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemangioblastoma, cerebellar, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebral-cerebellar-coloboma syndrome, x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral-cerebellar-coloboma syndrome, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

infantile cerebellar-retinal degeneration Gene Set

From OMIM Gene-Disease Associations

genes associated with the infantile cerebellar-retinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebellar Gene Set

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term cerebellar in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

cerebellar granule cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue cerebellar granule cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

cerebellar nucleus Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue cerebellar nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

cerebellar cortex Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue cerebellar cortex in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

cerebellar purkinje cell Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue cerebellar purkinje cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

Ataxia-telangiectasia-like disorder Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ataxia-telangiectasia-like disorder phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ataxia-telangiectasia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ataxia-telangiectasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia 28 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia 28 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia autosomal recessive 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia autosomal recessive 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Episodic ataxia, type 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Episodic ataxia, type 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ataxia, spastic, 4, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ataxia, spastic, 4, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia, autosomal recessive 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia, autosomal recessive 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ataxia with vitamin E deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ataxia with vitamin E deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ataxia, sensory, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ataxia, sensory, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia, autosomal recessive 15 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia, autosomal recessive 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia, autosomal recessive 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia, autosomal recessive 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia, autosomal recessive 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia, autosomal recessive 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia, autosomal recessive 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia, autosomal recessive 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic ataxia 5, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic ataxia 5, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Friedreich's ataxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Friedreich's ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic ataxia Charlevoix-Saguenay type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic ataxia Charlevoix-Saguenay type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Erythrokeratodermia with ataxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Erythrokeratodermia with ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia, X-linked 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia, X-linked 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leukoencephalopathy with ataxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leukoencephalopathy with ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Progressive myoclonus epilepsy with ataxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Progressive myoclonus epilepsy with ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia autosomal recessive with axonal neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia autosomal recessive with axonal neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ataxia-telangiectasia-like disorder 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ataxia-telangiectasia-like disorder 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ataxia-oculomotor apraxia 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ataxia-oculomotor apraxia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ataxia-telangiectasia variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ataxia-telangiectasia variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia, autosomal recessive 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia, autosomal recessive 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia, autosomal recessive 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia, autosomal recessive 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia, autosomal recessive 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia, autosomal recessive 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia 40 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia 40 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia 35 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia 35 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Adult onset ataxia with oculomotor apraxia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adult onset ataxia with oculomotor apraxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ataxia, spastic, 2, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ataxia, spastic, 2, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia autosomal recessive 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia autosomal recessive 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Episodic ataxia type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Episodic ataxia type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Episodic ataxia type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Episodic ataxia type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia 19 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia 19 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia 15 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia 21 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia 21 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia 27 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia 27 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia 26 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia 26 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia 29 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia 29 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia 38 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia 38 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar Ataxia 15 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar Ataxia 15 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar Ataxia 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar Ataxia 12 from the curated CTD Gene-Disease Associations dataset.

Ataxia Telangiectasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ataxia Telangiectasia from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar Ataxia 17 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar Ataxia 17 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar Ataxia 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar Ataxia 10 from the curated CTD Gene-Disease Associations dataset.

Gait Ataxia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gait Ataxia from the curated CTD Gene-Disease Associations dataset.

Ataxia, Spastic, 3, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ataxia, Spastic, 3, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Anemia, sideroblastic spinocerebellar ataxia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, sideroblastic spinocerebellar ataxia from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar Ataxia 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar Ataxia 11 from the curated CTD Gene-Disease Associations dataset.

Posterior column ataxia with retinitis pigmentosa Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Posterior column ataxia with retinitis pigmentosa from the curated CTD Gene-Disease Associations dataset.

Episodic ataxia with nystagmus Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Episodic ataxia with nystagmus from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia 26 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia 26 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia 28 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia 28 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar Ataxia, Autosomal Recessive 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar Ataxia, Autosomal Recessive 9 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar Ataxia, Autosomal Recessive 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar Ataxia, Autosomal Recessive 8 from the curated CTD Gene-Disease Associations dataset.

SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy from the curated CTD Gene-Disease Associations dataset.

Ataxia with vitamin E deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ataxia with vitamin E deficiency from the curated CTD Gene-Disease Associations dataset.

ATAXIA-TELANGIECTASIA-LIKE DISORDER 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ATAXIA-TELANGIECTASIA-LIKE DISORDER 1 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar Ataxia, X-Linked 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar Ataxia, X-Linked 5 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia 8 from the curated CTD Gene-Disease Associations dataset.

Spastic ataxia Charlevoix-Saguenay type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic ataxia Charlevoix-Saguenay type from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia, autosomal recessive 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia, autosomal recessive 3 from the curated CTD Gene-Disease Associations dataset.

Sensorimotor neuropathy with ataxia, autosomal dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sensorimotor neuropathy with ataxia, autosomal dominant from the curated CTD Gene-Disease Associations dataset.

Friedreich Ataxia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Friedreich Ataxia from the curated CTD Gene-Disease Associations dataset.

Episodic Ataxia, Type 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Episodic Ataxia, Type 3 from the curated CTD Gene-Disease Associations dataset.

Episodic Ataxia, Type 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Episodic Ataxia, Type 1 from the curated CTD Gene-Disease Associations dataset.

Episodic Ataxia, Type 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Episodic Ataxia, Type 7 from the curated CTD Gene-Disease Associations dataset.

Episodic Ataxia, Type 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Episodic Ataxia, Type 5 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia, autosomal recessive 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia, autosomal recessive 4 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia, autosomal recessive 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia, autosomal recessive 1 from the curated CTD Gene-Disease Associations dataset.

Ataxia, Spastic, 1, Autosomal Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ataxia, Spastic, 1, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia, X-linked, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia, X-linked, 4 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia, X-linked, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia, X-linked, 3 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia, X-linked, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia, X-linked, 2 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia, autosomal recessive 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia, autosomal recessive 6 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia, autosomal recessive 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia, autosomal recessive 5 from the curated CTD Gene-Disease Associations dataset.

Episodic Ataxia, Type 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Episodic Ataxia, Type 6 from the curated CTD Gene-Disease Associations dataset.

Friedreich Ataxia 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Friedreich Ataxia 1 from the curated CTD Gene-Disease Associations dataset.

Friedreich Ataxia 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Friedreich Ataxia 2 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar Ataxia, Autosomal Recessive 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar Ataxia, Autosomal Recessive 2 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia 13 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia 13 from the curated CTD Gene-Disease Associations dataset.

Fragile X Tremor Ataxia Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fragile X Tremor Ataxia Syndrome from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia 20 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia 20 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar Ataxia 29 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar Ataxia 29 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia 23 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia 23 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia 21 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia 21 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia 27 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia 27 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia 25 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia 25 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia 14 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia 14 from the curated CTD Gene-Disease Associations dataset.

Ataxia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ataxia from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar Ataxia 31 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar Ataxia 31 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia 30 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia 30 from the curated CTD Gene-Disease Associations dataset.

infantile onset spinocerebellar ataxia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease infantile onset spinocerebellar ataxia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

episodic ataxia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease episodic ataxia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

ataxia telangiectasia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease ataxia telangiectasia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

x-linked sideroblastic anemia with ataxia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease x-linked sideroblastic anemia with ataxia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

spinocerebellar ataxia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease spinocerebellar ataxia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

friedreich ataxia Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease friedreich ataxia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

infantile onset spinocerebellar ataxia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease infantile onset spinocerebellar ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

friedreich ataxia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease friedreich ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

sideroblastic anemia with spinocerebellar ataxia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease sideroblastic anemia with spinocerebellar ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

ataxia telangiectasia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease ataxia telangiectasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

x-linked sideroblastic anemia with ataxia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease x-linked sideroblastic anemia with ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

spinocerebellar ataxia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease spinocerebellar ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

episodic ataxia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease episodic ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

ataxia with oculomotor apraxia type 1 Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease ataxia with oculomotor apraxia type 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

ataxia with oculomotor apraxia type 2 Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease ataxia with oculomotor apraxia type 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

essential tremor; cerebral ataxia; multiple-system atropy; parkinsonism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease essential tremor; cerebral ataxia; multiple-system atropy; parkinsonism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

schizophrenia; ataxia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease schizophrenia; ataxia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomegaly; friedreich ataxia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomegaly; friedreich ataxia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinocerebellar ataxia type 6 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinocerebellar ataxia type 6 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ataxia telangiectasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ataxia telangiectasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinocerebellar ataxia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinocerebellar ataxia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

spinocerebellar ataxia; muscular dystrophy; neuropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spinocerebellar ataxia; muscular dystrophy; neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fragile x associated tremor/ataxia syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fragile x associated tremor/ataxia syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ataxia telangiectasia; louis-bar syndrome; lymphoma, non-hodgkin; lymphoma, non-hodgkin's Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ataxia telangiectasia; louis-bar syndrome; lymphoma, non-hodgkin; lymphoma, non-hodgkin's in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ataxia-telangiectasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ataxia-telangiectasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

friedreich ataxia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease friedreich ataxia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carotid artery intima-media thickness; spinocerebellar ataxia; huntington's disease; myotonic dystrophy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carotid artery intima-media thickness; spinocerebellar ataxia; huntington's disease; myotonic dystrophy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

parkinsons disease; alzheimers disease; ataxia; huntingtons disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease parkinsons disease; alzheimers disease; ataxia; huntingtons disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ataxia telangiectasia; fragile x syndrome; tremor Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ataxia telangiectasia; fragile x syndrome; tremor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathies; friedreich ataxia; scoliosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathies; friedreich ataxia; scoliosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

episodic ataxia type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease episodic ataxia type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

huntington's disease; ataxia (sca) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease huntington's disease; ataxia (sca) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fragile x-associated tremor/ataxia syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fragile x-associated tremor/ataxia syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ataxia; fragile x syndrome; huntington disease; tremor Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ataxia; fragile x syndrome; huntington disease; tremor in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ataxia telangiectasia; neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ataxia telangiectasia; neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ataxia (sca) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ataxia (sca) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosomal instability; friedreich ataxia; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosomal instability; friedreich ataxia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ataxia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ataxia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ataxia; fragile x syndrome; fragile x syndromes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ataxia; fragile x syndrome; fragile x syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ataxia telangiectasia; carcinoma, squamous cell; mouth neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ataxia telangiectasia; carcinoma, squamous cell; mouth neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; ataxia; diabetes mellitus, type 2; disease; obesity; parkinson disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; ataxia; diabetes mellitus, type 2; disease; obesity; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gait ataxia; parkinson disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gait ataxia; parkinson disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

friedreichs ataxia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease friedreichs ataxia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ataxia Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term ataxia in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

spastic ataxia Gene Set

From HPO Gene-Disease Associations

genes associated with the spastic ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

gait ataxia Gene Set

From HPO Gene-Disease Associations

genes associated with the gait ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

limb ataxia Gene Set

From HPO Gene-Disease Associations

genes associated with the limb ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

episodic ataxia Gene Set

From HPO Gene-Disease Associations

genes associated with the episodic ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ataxia Gene Set

From HPO Gene-Disease Associations

genes associated with the ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

progressive gait ataxia Gene Set

From HPO Gene-Disease Associations

genes associated with the progressive gait ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

sensory ataxia Gene Set

From HPO Gene-Disease Associations

genes associated with the sensory ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

progressive truncal ataxia Gene Set

From HPO Gene-Disease Associations

genes associated with the progressive truncal ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

truncal ataxia Gene Set

From HPO Gene-Disease Associations

genes associated with the truncal ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Gait Ataxia Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Gait Ataxia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Ataxia Telangiectasia Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Ataxia Telangiectasia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Friedreich Ataxia Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Friedreich Ataxia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Ataxia Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Ataxia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

ataxia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the ataxia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

?spinocerebellar ataxia, autosomal recessive 15 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?spinocerebellar ataxia, autosomal recessive 15 phenotype from the curated OMIM Gene-Disease Associations dataset.

?spinocerebellar ataxia, autosomal recessive 17 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?spinocerebellar ataxia, autosomal recessive 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

ataxia with isolated vitamin e deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ataxia with isolated vitamin e deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

episodic ataxia, type 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the episodic ataxia, type 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

episodic ataxia, type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the episodic ataxia, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

episodic ataxia, type 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the episodic ataxia, type 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

episodic ataxia, type 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the episodic ataxia, type 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

episodic ataxia, type 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the episodic ataxia, type 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic ataxia 2, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic ataxia 2, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic ataxia 3, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic ataxia 3, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

?spinocerebellar ataxia 34 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?spinocerebellar ataxia 34 phenotype from the curated OMIM Gene-Disease Associations dataset.

?spinocerebellar ataxia 30 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?spinocerebellar ataxia 30 phenotype from the curated OMIM Gene-Disease Associations dataset.

anemia, sideroblastic, with ataxia Gene Set

From OMIM Gene-Disease Associations

genes associated with the anemia, sideroblastic, with ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia, autosomal recessive 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia, autosomal recessive 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia, autosomal recessive 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia, autosomal recessive 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia, autosomal recessive 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia, autosomal recessive 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia, autosomal recessive 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia, autosomal recessive 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia 18 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia 18 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia 19 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia 19 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia 17 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia 15 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia 15 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

ataxia-telangiectasia-like disorder Gene Set

From OMIM Gene-Disease Associations

genes associated with the ataxia-telangiectasia-like disorder phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia 35 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia 35 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia 36 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia 36 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia 31 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia 31 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia 32 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia 32 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia 38 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia 38 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocrebellar ataxia, autosomal recessive 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocrebellar ataxia, autosomal recessive 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

leukoencephalopathy with ataxia Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukoencephalopathy with ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.

ataxia-telangiectasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ataxia-telangiectasia phenotype from the curated OMIM Gene-Disease Associations dataset.

?ataxia-telangiectasia-like disorder Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?ataxia-telangiectasia-like disorder phenotype from the curated OMIM Gene-Disease Associations dataset.

friedreich ataxia Gene Set

From OMIM Gene-Disease Associations

genes associated with the friedreich ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia, autosomal recessive 16 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia, autosomal recessive 16 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia, autosomal recessive 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia, autosomal recessive 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia, autosomal recessive 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia, autosomal recessive 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia, autosomal recessive 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia, autosomal recessive 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia, autosomal recessive 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia, autosomal recessive 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia, x-linked 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia, x-linked 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic ataxia 1, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic ataxia 1, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

fragile x tremor/ataxia syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the fragile x tremor/ataxia syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

ataxia, posterior column, with retinitis pigmentosa Gene Set

From OMIM Gene-Disease Associations

genes associated with the ataxia, posterior column, with retinitis pigmentosa phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia, autosomal recessive 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia, autosomal recessive 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

friedreich ataxia with retained reflexes Gene Set

From OMIM Gene-Disease Associations

genes associated with the friedreich ataxia with retained reflexes phenotype from the curated OMIM Gene-Disease Associations dataset.

ataxia-ocular apraxia-2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ataxia-ocular apraxia-2 phenotype from the curated OMIM Gene-Disease Associations dataset.

?spinocerebellar ataxia 40 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?spinocerebellar ataxia 40 phenotype from the curated OMIM Gene-Disease Associations dataset.

?spinocerebellar ataxia 26 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?spinocerebellar ataxia 26 phenotype from the curated OMIM Gene-Disease Associations dataset.

ataxia-oculomotor apraxia 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ataxia-oculomotor apraxia 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

?spinocerebellar ataxia, x-linked 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?spinocerebellar ataxia, x-linked 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

ataxia, sensory, 1, autosomal dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the ataxia, sensory, 1, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia 23 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia 23 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia 21 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia 21 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia 20 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia 20 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia 27 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia 27 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia 25 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia 25 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia 28 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia 28 phenotype from the curated OMIM Gene-Disease Associations dataset.

episodic ataxia/myokymia syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the episodic ataxia/myokymia syndrome phenotype from the curated OMIM Gene-Disease Associat