Name

Facial Paralysis Gene Set

From CTD Gene-Disease Associations

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

facial paralysis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

facial paralysis Gene Set

From HPO Gene-Disease Associations

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

Facial Paralysis Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Normokalemic periodic paralysis, potassium-sensitive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Normokalemic periodic paralysis, potassium-sensitive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thyrotoxic periodic paralysis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thyrotoxic periodic paralysis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypokalemic periodic paralysis, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypokalemic periodic paralysis, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypokalemic periodic paralysis 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypokalemic periodic paralysis 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperkalemic Periodic Paralysis Type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperkalemic Periodic Paralysis Type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile-onset ascending hereditary spastic paralysis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile-onset ascending hereditary spastic paralysis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 2 from the curated CTD Gene-Disease Associations dataset.

Hereditary spastic paralysis, infantile onset ascending Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hereditary spastic paralysis, infantile onset ascending from the curated CTD Gene-Disease Associations dataset.

Laryngeal Adductor Paralysis Gene Set

From CTD Gene-Disease Associations

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

Paralysis, Hyperkalemic Periodic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Paralysis, Hyperkalemic Periodic from the curated CTD Gene-Disease Associations dataset.

Paralysis Gene Set

From CTD Gene-Disease Associations

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

THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THYROTOXIC PERIODIC PARALYSIS, SUSCEPTIBILITY TO, 1 from the curated CTD Gene-Disease Associations dataset.

Hypokalemic Periodic Paralysis, Type 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypokalemic Periodic Paralysis, Type 2 from the curated CTD Gene-Disease Associations dataset.

HYPOKALEMIC PERIODIC PARALYSIS, TYPE 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HYPOKALEMIC PERIODIC PARALYSIS, TYPE 1 from the curated CTD Gene-Disease Associations dataset.

Respiratory Paralysis Gene Set

From CTD Gene-Disease Associations

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

Vocal Cord Paralysis Gene Set

From CTD Gene-Disease Associations

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

Hypokalemic Periodic Paralysis Gene Set

From CTD Gene-Disease Associations

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

hyperkalemic periodic paralysis Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

hypokalemic periodic paralysis Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

familial periodic paralysis Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

peroneal nerve paralysis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hyperkalemic periodic paralysis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hypokalemic periodic paralysis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

familial periodic paralysis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

oculomotor nerve paralysis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

tick paralysis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

spastic paralysis Gene Set

From GAD Gene-Disease Associations

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

paralysis; sensation disorders; spinal cord injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease paralysis; sensation disorders; spinal cord injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

periodic paralysis Gene Set

From GAD Gene-Disease Associations

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

infantile-onset ascending hereditary spastic paralysis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infantile-onset ascending hereditary spastic paralysis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

paralysis Gene Set

From GAD Gene-Disease Associations

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

thyrotoxic periodic paralysis Gene Set

From GAD Gene-Disease Associations

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

paralysis Gene Set

From GeneRIF Biological Term Annotations

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

vocal cord paralysis (caused by tumor impingement) Gene Set

From HPO Gene-Disease Associations

genes associated with the vocal cord paralysis (caused by tumor impingement) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

pseudobulbar paralysis Gene Set

From HPO Gene-Disease Associations

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

cranial nerve paralysis Gene Set

From HPO Gene-Disease Associations

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

diaphragmatic paralysis Gene Set

From HPO Gene-Disease Associations

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

vocal cord paralysis Gene Set

From HPO Gene-Disease Associations

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

periodic hyperkalemic paralysis Gene Set

From HPO Gene-Disease Associations

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

respiratory paralysis Gene Set

From HPO Gene-Disease Associations

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

periodic paralysis Gene Set

From HPO Gene-Disease Associations

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

paralysis Gene Set

From HPO Gene-Disease Associations

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

Paralysis, Hyperkalemic Periodic Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Paralysis, Hyperkalemic Periodic phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Respiratory Paralysis Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Hypokalemic Periodic Paralysis Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hypokalemic Periodic Paralysis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

forelimb paralysis Gene Set

From MPO Gene-Phenotype Associations

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

hindlimb paralysis Gene Set

From MPO Gene-Phenotype Associations

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

paralysis Gene Set

From MPO Gene-Phenotype Associations

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

hyperkalemic periodic paralysis, type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperkalemic periodic paralysis, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

{thyrotoxic periodic paralysis, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {thyrotoxic periodic paralysis, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

?laryngeal adductor paralysis Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?laryngeal adductor paralysis phenotype from the curated OMIM Gene-Disease Associations dataset.

{thyrotoxic periodic paralysis, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {thyrotoxic periodic paralysis, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

hypokalemic periodic paralysis, type 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypokalemic periodic paralysis, type 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

hypokalemic periodic paralysis, type 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypokalemic periodic paralysis, type 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paralysis, infantile onset ascending Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paralysis, infantile onset ascending phenotype from the curated OMIM Gene-Disease Associations dataset.

facial motor nucleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in facial motor nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

facial motor nucleus, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in facial motor nucleus, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

Facial motor nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

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

Accessory facial motor nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

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

facial nucleus Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

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

Facial paresis, hereditary congenital, 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Facial paresis, hereditary congenital, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Facial dysmorphism, immunodeficiency, livedo, and short stature Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Facial dysmorphism, immunodeficiency, livedo, and short stature phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Macrocephaly, macrosomia, facial dysmorphism syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Macrocephaly, macrosomia, facial dysmorphism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype 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.

Oral-facial-digital syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Oral-facial-digital syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Infantile neuroaxonal neurodegeneration with facial dysmorphism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Infantile neuroaxonal neurodegeneration with facial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency-centromeric instability-facial anomalies syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency-centromeric instability-facial anomalies syndrome 2 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.

Congenital Cataracts, Facial Dysmorphism, and Neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital Cataracts, Facial Dysmorphism, and Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 1 from the curated CTD Gene-Disease Associations dataset.

Facial paresis, hereditary, congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Facial paresis, hereditary, congenital from the curated CTD Gene-Disease Associations dataset.

Malpuech facial clefting syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Malpuech facial clefting syndrome from the curated CTD Gene-Disease Associations dataset.

AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AUTOIMMUNE DISEASE, MULTISYSTEM, WITH FACIAL DYSMORPHISM from the curated CTD Gene-Disease Associations dataset.

Congenital Cataracts, Facial Dysmorphism, And Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Cataracts, Facial Dysmorphism, And Neuropathy from the curated CTD Gene-Disease Associations dataset.

Facial Dermatoses Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Facial Dermatoses from the curated CTD Gene-Disease 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.

Facial Asymmetry Gene Set

From CTD Gene-Disease Associations

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

Facial Pain Gene Set

From CTD Gene-Disease Associations

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

facial hemiatrophy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

facial dermatosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

cranio-facial dystonia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

facial neuralgia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

lingual-facial-buccal dyskinesia Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

facial nerve disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

negative affective facial stimuli Gene Set

From GAD Gene-Disease Associations

genes associated with the disease negative affective facial stimuli in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

degenerative arthropathy ; facial pain; osteoarthritis; temporomandibular joint disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease degenerative arthropathy ; facial pain; osteoarthritis; temporomandibular joint disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

psychiatric manifestations of velo-cardio-facial syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease psychiatric manifestations of velo-cardio-facial syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

facial neoplasms; horse diseases; melanoma; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease facial neoplasms; horse diseases; melanoma; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

severe photoaging of facial skin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease severe photoaging of facial skin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

facial Gene Set

From GeneRIF Biological Term Annotations

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

facial nerve morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the facial nerve morphogenesis biological process from the curated GO Biological Process Annotations dataset.

facial nerve structural organization Gene Set

From GO Biological Process Annotations

genes participating in the facial nerve structural organization biological process from the curated GO Biological Process Annotations dataset.

facial nucleus development Gene Set

From GO Biological Process Annotations

genes participating in the facial nucleus development biological process from the curated GO Biological Process Annotations dataset.

Facial morphology Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Facial morphology phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

facial dermatosis Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease facial dermatosis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

abnormality of facial skeleton Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of facial skeleton phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal facial shape Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal facial shape phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

decreased facial expression Gene Set

From HPO Gene-Disease Associations

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

facial wrinkling Gene Set

From HPO Gene-Disease Associations

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

loss of facial expression Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of facial expression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

facial palsy Gene Set

From HPO Gene-Disease Associations

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

facial diplegia Gene Set

From HPO Gene-Disease Associations

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

absent facial hair Gene Set

From HPO Gene-Disease Associations

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

facial hemangioma Gene Set

From HPO Gene-Disease Associations

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

midline facial capillary hemangioma Gene Set

From HPO Gene-Disease Associations

genes associated with the midline facial capillary hemangioma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

facial shape deformation Gene Set

From HPO Gene-Disease Associations

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

midline facial cleft Gene Set

From HPO Gene-Disease Associations

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

facial asymmetry Gene Set

From HPO Gene-Disease Associations

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

facial hypotonia Gene Set

From HPO Gene-Disease Associations

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

abnormality of facial soft tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of facial soft tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spasticity of facial muscles Gene Set

From HPO Gene-Disease Associations

genes associated with the spasticity of facial muscles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

facial telangiectasia in butterfly midface distribution Gene Set

From HPO Gene-Disease Associations

genes associated with the facial telangiectasia in butterfly midface distribution phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

facial palsy secondary to cranial hyperostosis Gene Set

From HPO Gene-Disease Associations

genes associated with the facial palsy secondary to cranial hyperostosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

facial capillary hemangioma Gene Set

From HPO Gene-Disease Associations

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

abnormal facial shape Gene Set

From HPO Gene-Disease Associations

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

sleepy facial expression Gene Set

From HPO Gene-Disease Associations

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

facial flushing after alcohol intake Gene Set

From HPO Gene-Disease Associations

genes associated with the facial flushing after alcohol intake phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

disturbance of facial expression Gene Set

From HPO Gene-Disease Associations

genes associated with the disturbance of facial expression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of facial adipose tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of facial adipose tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

facial telangiectasia Gene Set

From HPO Gene-Disease Associations

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

facial cleft Gene Set

From HPO Gene-Disease Associations

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

facial myokymia Gene Set

From HPO Gene-Disease Associations

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

facial hirsutism Gene Set

From HPO Gene-Disease Associations

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

sparse facial hair Gene Set

From HPO Gene-Disease Associations

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

abnormal facial expression Gene Set

From HPO Gene-Disease Associations

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

abnormality of facial skeleton Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of facial skeleton phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

coarse facial features Gene Set

From HPO Gene-Disease Associations

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

abnormality of facial musculature Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of facial musculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

increased facial adipose tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the increased facial adipose tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

facial erythema Gene Set

From HPO Gene-Disease Associations

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

facial grimacing Gene Set

From HPO Gene-Disease Associations

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

loss of facial adipose tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of facial adipose tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

fixed facial expression Gene Set

From HPO Gene-Disease Associations

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

hypoplastic facial bones Gene Set

From HPO Gene-Disease Associations

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

facial hyperostosis Gene Set

From HPO Gene-Disease Associations

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

progeroid facial appearance Gene Set

From HPO Gene-Disease Associations

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

facial edema Gene Set

From HPO Gene-Disease Associations

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

facial hypertrichosis Gene Set

From HPO Gene-Disease Associations

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

facial-lingual fasciculations Gene Set

From HPO Gene-Disease Associations

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

Facial Neoplasms Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Facial Asymmetry Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Facial Pain Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Armadillo repeat protein deleted in velo-cardio-facial syndrome Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Armadillo repeat protein deleted in velo-cardio-facial syndrome protein domain from the InterPro Predicted Protein Domain Annotations dataset.

absent facial nuclei Gene Set

From MPO Gene-Phenotype Associations

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

abnormal facial nerve morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal facial nerve morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

midline facial cleft Gene Set

From MPO Gene-Phenotype Associations

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

absent facial nerve Gene Set

From MPO Gene-Phenotype Associations

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

abnormal facial motor nucleus morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal facial motor nucleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small facial motor nucleus Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small facial motor nucleus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased facial tumor incidence Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased facial tumor incidence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal facial morphology Gene Set

From MPO Gene-Phenotype Associations

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

oblique facial cleft Gene Set

From MPO Gene-Phenotype Associations

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

facial cleft Gene Set

From MPO Gene-Phenotype Associations

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

myasthenic syndrome, congenital, associated with facial dysmorphism and acetylcholine receptor deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenic syndrome, congenital, associated with facial dysmorphism and acetylcholine receptor deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

short stature, onychodysplasia, facial dysmorphism, and hypotrichosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the short stature, onychodysplasia, facial dysmorphism, and hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency-centromeric instability-facial anomalies syndrome-2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency-centromeric instability-facial anomalies syndrome-2 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.

neuroaxonal neurodegeneration, infantile, with facial dysmophism Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuroaxonal neurodegeneration, infantile, with facial dysmophism phenotype from the curated OMIM Gene-Disease Associations dataset.

dyskinesia, familial, with facial myokymia Gene Set

From OMIM Gene-Disease Associations

genes associated with the dyskinesia, familial, with facial myokymia phenotype from the curated OMIM Gene-Disease Associations dataset.

facial paresis, hereditary congenital, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the facial paresis, hereditary congenital, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

facial clefting, oblique, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the facial clefting, oblique, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital cataracts, facial dysmorphism, and neuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital cataracts, facial dysmorphism, and neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

macrocephaly, macrosomia, facial dysmorphism syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the macrocephaly, macrosomia, facial dysmorphism syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

focal facial dermal dysplasia 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the focal facial dermal dysplasia 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

autoimmune disease, multisystem, with facial dysmorphism Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoimmune disease, multisystem, with facial dysmorphism phenotype from the curated OMIM Gene-Disease Associations dataset.

aplasia cutis congenita, reticulolinear, with mmicrocephaly, facial dysmorphism and other congenital anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the aplasia cutis congenita, reticulolinear, with mmicrocephaly, facial dysmorphism and other congenital anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency-centromeric instability-facial anomalies syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency-centromeric instability-facial anomalies syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

nablus mask-like facial syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the nablus mask-like facial syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

focal facial dermal dysplasia 3, setleis type Gene Set

From OMIM Gene-Disease Associations

genes associated with the focal facial dermal dysplasia 3, setleis type phenotype from the curated OMIM Gene-Disease Associations dataset.

Defective CYP26C1 causes Focal facial dermal dysplasia 4 (FFDD4) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP26C1 causes Focal facial dermal dysplasia 4 (FFDD4) pathway from the Reactome Pathways dataset.