Name

abnormal short term spatial reference memory Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal short term spatial reference memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal long term spatial reference memory Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal long term spatial reference memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spatial reference memory Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spatial reference memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal short term object recognition memory Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal short term object recognition memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Memory, Short-Term Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Memory, Short-Term in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

memory, short-term Gene Set

From GAD Gene-Disease Associations

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

short-term memory Gene Set

From GO Biological Process Annotations

genes participating in the short-term memory biological process from the curated GO Biological Process Annotations dataset.

Memory, Short-Term Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Memory, Short-Term phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

abnormal spatial working memory Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spatial working memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal long term object recognition memory Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal long term object recognition memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

human long-term memory Gene Set

From GAD Gene-Disease Associations

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

long-term memory Gene Set

From GO Biological Process Annotations

genes participating in the long-term memory biological process from the curated GO Biological Process Annotations dataset.

Memory, Long-Term Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Memory, Long-Term phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

short-term response to haloperidol treatment Gene Set

From GAD Gene-Disease Associations

genes associated with the disease short-term response to haloperidol treatment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

regulation of short-term neuronal synaptic plasticity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of short-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations dataset.

abnormal spatial orientation of the cardiac segments Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal spatial orientation of the cardiac segments phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal spatial learning Gene Set

From MPO Gene-Phenotype Associations

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

reference Gene Set

From GeneRIF Biological Term Annotations

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

SPATIAL VISUALIZATION, APTITUDE FOR Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPATIAL VISUALIZATION, APTITUDE FOR from the curated CTD Gene-Disease Associations dataset.

spatial Gene Set

From GeneRIF Biological Term Annotations

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

impaired spatial learning Gene Set

From MPO Gene-Phenotype Associations

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

enhanced spatial learning Gene Set

From MPO Gene-Phenotype Associations

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

childhood-onset short-trunk short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the childhood-onset short-trunk short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

neonatal short-trunk short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the neonatal short-trunk short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

disproportionate short-trunk short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the disproportionate short-trunk short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

disproportionate short-limb short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the disproportionate short-limb short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lethal short-limbed short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the lethal short-limbed short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

childhood onset short-limb short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the childhood onset short-limb short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

neonatal short-limb short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the neonatal short-limb short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal long term potentiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal long term potentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal long term depression Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal long term depression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

the prc2 complex sets long-term gene silencing through modification of histone tails Gene Set

From Biocarta Pathways

proteins participating in the the prc2 complex sets long-term gene silencing through modification of histone tails pathway from the Biocarta Pathways dataset.

pre-term delivery infant mortality and malaria morbidity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pre-term delivery infant mortality and malaria morbidity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

delayed graft function acute rejection episodes and long-term graft dysfunction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease delayed graft function acute rejection episodes and long-term graft dysfunction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

long-term kidney allograft survival Gene Set

From GAD Gene-Disease Associations

genes associated with the disease long-term kidney allograft survival in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

term Gene Set

From GeneRIF Biological Term Annotations

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

regulation of long term synaptic depression Gene Set

From GO Biological Process Annotations

genes participating in the regulation of long term synaptic depression biological process from the curated GO Biological Process Annotations dataset.

regulation of long-term synaptic potentiation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of long-term synaptic potentiation biological process from the curated GO Biological Process Annotations dataset.

positive regulation of long-term synaptic potentiation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of long-term synaptic potentiation biological process from the curated GO Biological Process Annotations dataset.

regulation of long-term neuronal synaptic plasticity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of long-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations dataset.

long term synaptic depression Gene Set

From GO Biological Process Annotations

genes participating in the long term synaptic depression biological process from the curated GO Biological Process Annotations dataset.

long-term synaptic potentiation Gene Set

From GO Biological Process Annotations

genes participating in the long-term synaptic potentiation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of long term synaptic depression Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of long term synaptic depression biological process from the curated GO Biological Process Annotations dataset.

positive regulation of long-term neuronal synaptic plasticity Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of long-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations dataset.

Pre-mRNA 3'-end-processing endonuclease polyadenylation factor C-term Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Pre-mRNA 3'-end-processing endonuclease polyadenylation factor C-term protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cytoplasmic activation/proliferation-associated protein-1 C term Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cytoplasmic activation/proliferation-associated protein-1 C term protein domain from the InterPro Predicted Protein Domain Annotations dataset.

G protein-coupled receptor kinase-interacting protein 1 C term Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the G protein-coupled receptor kinase-interacting protein 1 C term protein domain from the InterPro Predicted Protein Domain Annotations dataset.

long term depression Gene Set

From KEGG Pathways

proteins participating in the long term depression pathway from the KEGG Pathways dataset.

long term potentiation Gene Set

From KEGG Pathways

proteins participating in the long term potentiation pathway from the KEGG Pathways dataset.

absent long term depression Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent long term depression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

enhanced long term potentiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the enhanced long term potentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

reduced long term potentiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the reduced long term potentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

reduced long term depression Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the reduced long term depression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal memory t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal object recognition memory Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal object recognition memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal memory t cell physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal memory t cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal memory b cell differentiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal memory b cell differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal olfactory -discrimination memory Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal olfactory -discrimination memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal learning/memory/conditioning Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal learning/memory/conditioning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal memory b cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cd4-positive, alpha-beta memory t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cd4-positive, alpha-beta memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal effector memory cd4-positive, alpha-beta t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal effector memory cd4-positive, alpha-beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal memory b cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal memory b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal memory t cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal effector memory cd4-positive, alpha-beta t cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal effector memory cd4-positive, alpha-beta t cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cd8-positive, alpha-beta memory t cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cd8-positive, alpha-beta memory t cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cd8-positive, alpha-beta memory t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cd8-positive, alpha-beta memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal temporal memory Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cd4-positive, alpha-beta memory t cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cd4-positive, alpha-beta memory t cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal effector memory cd8-positive, alpha-beta t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal effector memory cd8-positive, alpha-beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal memory b cell physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal memory b cell physiology phenotype in transgenic mice from the MPO 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.

Memory Disorders Gene Set

From CTD Gene-Disease Associations

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

Memory Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Memory in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

memory disorders Gene Set

From GAD Gene-Disease Associations

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

cerebral infarction; memory disorders; subarachnoid hemorrhage Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarction; memory disorders; subarachnoid hemorrhage in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anxiety disorder; blood pressure, arterial; memory impairment Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anxiety disorder; blood pressure, arterial; memory impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

memory decline Gene Set

From GAD Gene-Disease Associations

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

dementia; memory disorders; stroke Gene Set

From GAD Gene-Disease Associations

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

dementia; memory disorders Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; memory disorders; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

memory impairment, subjective Gene Set

From GAD Gene-Disease Associations

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

memory disturbance Gene Set

From GAD Gene-Disease Associations

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

amnesia; memory disorders Gene Set

From GAD Gene-Disease Associations

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

memory disorders; recurrence Gene Set

From GAD Gene-Disease Associations

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

memory performance. Gene Set

From GAD Gene-Disease Associations

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

memory impairment Gene Set

From GAD Gene-Disease Associations

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

epilepsy, temporal lobe; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease epilepsy, temporal lobe; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; disorders of excessive somnolence; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; disorders of excessive somnolence; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anticholinergic challenge-induced memory impairment Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anticholinergic challenge-induced memory impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; dementia; memory disorders Gene Set

From GAD Gene-Disease Associations

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

memory disorders; sleep apnea syndromes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease memory disorders; sleep apnea syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

digeorge syndrome; memory disorders; pharyngeal pouch; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease digeorge syndrome; memory disorders; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

synaptogenesis and memory. Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brain injuries; memory disorders Gene Set

From GAD Gene-Disease Associations

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

verbal learning, verbal memory, and regional cortical gray matter density Gene Set

From GAD Gene-Disease Associations

genes associated with the disease verbal learning, verbal memory, and regional cortical gray matter density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; atrophy; dementia; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; atrophy; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrophy; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrophy; memory disorders 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.

asthma; lipids; memory impairment Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; lipids; memory impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; atrophy; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

memory disorders; prenatal exposure delayed effects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease memory disorders; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

irritability hostility impulsivity and memory Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; dementia; hypothyroidism; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; dementia; hypothyroidism; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; memory disorders Gene Set

From GAD Gene-Disease Associations

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

insulin; smoking behavior; obesity, localized; memory disturbance; longevity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin; smoking behavior; obesity, localized; memory disturbance; longevity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral hemorrhage; cerebral hemorrhages; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral hemorrhage; cerebral hemorrhages; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

age-associated memory impairment Gene Set

From GAD Gene-Disease Associations

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

inflammation; memory disorders Gene Set

From GAD Gene-Disease Associations

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

working memory Gene Set

From GAD Gene-Disease Associations

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

memory Gene Set

From GAD Gene-Disease Associations

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

apoplexy; memory disorders; stroke Gene Set

From GAD Gene-Disease Associations

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

age-associated memory impairment (aami) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease age-associated memory impairment (aami) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

episodic memory Gene Set

From GAD Gene-Disease Associations

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

memory function Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; memory disorders Gene Set

From GAD Gene-Disease Associations

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

chronic progressive chorea; memory disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic progressive chorea; memory disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

memory performance Gene Set

From GAD Gene-Disease Associations

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

memory disorders; mercury poisoning, nervous system; occupational diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease memory disorders; mercury poisoning, nervous system; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

memorydiscrepant Gene Set

From GeneRIF Biological Term Annotations

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

memoryeffector Gene Set

From GeneRIF Biological Term Annotations

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

memoryassociated Gene Set

From GeneRIF Biological Term Annotations

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

memoryrelated Gene Set

From GeneRIF Biological Term Annotations

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

memorylike Gene Set

From GeneRIF Biological Term Annotations

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

memory Gene Set

From GeneRIF Biological Term Annotations

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

negative regulation of memory t cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of memory t cell differentiation biological process from the curated GO Biological Process Annotations dataset.

learning or memory Gene Set

From GO Biological Process Annotations

genes participating in the learning or memory biological process from the curated GO Biological Process Annotations dataset.

regulation of memory t cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of memory t cell differentiation biological process from the curated GO Biological Process Annotations dataset.

positive regulation of memory t cell activation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of memory t cell activation biological process from the curated GO Biological Process Annotations dataset.

memory t cell proliferation Gene Set

From GO Biological Process Annotations

genes participating in the memory t cell proliferation biological process from the curated GO Biological Process Annotations dataset.

memory t cell activation Gene Set

From GO Biological Process Annotations

genes participating in the memory t cell activation biological process from the curated GO Biological Process Annotations dataset.

positive regulation of memory t cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of memory t cell differentiation biological process from the curated GO Biological Process Annotations dataset.

memory Gene Set

From GO Biological Process Annotations

genes participating in the memory biological process from the curated GO Biological Process Annotations dataset.

regulation of memory t cell activation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of memory t cell activation biological process from the curated GO Biological Process Annotations dataset.

Response to antipsychotic treatment in schizophrenia (working memory) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Response to antipsychotic treatment in schizophrenia (working memory) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Memory performance Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

memory impairment Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the memory impairment phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

impaired memory b-cell generation Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired memory b-cell generation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

memory impairment Gene Set

From HPO Gene-Disease Associations

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

Memory Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Memory Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

decreased memory t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased cd4-positive, alpha-beta memory t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased cd4-positive, alpha-beta memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent memory b cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent memory b cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased memory b cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased memory b cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased effector memory cd8-positive, alpha-beta t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased effector memory cd8-positive, alpha-beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased memory t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased effector memory cd4-positive, alpha-beta t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased effector memory cd4-positive, alpha-beta t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

slow extinction of fear memory Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the slow extinction of fear memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased cd4-positive, alpha-beta memory t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cd4-positive, alpha-beta memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased cd8-positive, alpha-beta memory t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cd8-positive, alpha-beta memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased cd8-positive, alpha-beta memory t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased cd8-positive, alpha-beta memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

{memory impairment, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {memory impairment, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

[memory, enhanced, qtl] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [memory, enhanced, qtl] phenotype from the curated OMIM Gene-Disease Associations dataset.

memory Gene Set

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term memory in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

H3K27me3_CD4 Memory Primary Cells Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K27me3_CD4 Memory Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K27ac_CD4 Memory Primary Cells Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K27ac_CD4 Memory Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K4me1_CD4+ CD25- CD45RO+ Memory Primary Cells Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me1_CD4+ CD25- CD45RO+ Memory Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K36me3_CD8 Memory Primary Cells Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K36me3_CD8 Memory Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K9me3_CD4+ CD25- CD45RO+ Memory Primary Cells Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K9me3_CD4+ CD25- CD45RO+ Memory Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K36me3_CD4 Memory Primary Cells Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K36me3_CD4 Memory Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K4me3_CD4 Memory Primary Cells Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me3_CD4 Memory Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K4me1_CD8 Memory Primary Cells Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me1_CD8 Memory Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K9me3_CD4 Memory Primary Cells Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K9me3_CD4 Memory Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K27me3_CD8 Memory Primary Cells Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K27me3_CD8 Memory Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K36me3_CD4+ CD25- CD45RO+ Memory Primary Cells Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K36me3_CD4+ CD25- CD45RO+ Memory Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K4me3_CD8 Memory Primary Cells Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me3_CD8 Memory Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K27ac_CD8 Memory Primary Cells Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K27ac_CD8 Memory Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K27me3_CD4+ CD25- CD45RO+ Memory Primary Cells Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K27me3_CD4+ CD25- CD45RO+ Memory Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K9me3_CD8 Memory Primary Cells Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K9me3_CD8 Memory Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K27ac_CD4+ CD25- CD45RO+ Memory Primary Cells Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K27ac_CD4+ CD25- CD45RO+ Memory Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K4me1_CD4 Memory Primary Cells Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me1_CD4 Memory Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K4me3_CD4+ CD25- CD45RO+ Memory Primary Cells Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me3_CD4+ CD25- CD45RO+ Memory Primary Cells histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

memory t-lymphocyte Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue memory t-lymphocyte in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

short insular gyri, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

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

short insular gyri, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

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

Short stature, idiopathic, autosomal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, idiopathic, autosomal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short rib-polydactyly syndrome, Majewski type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short rib-polydactyly syndrome, Majewski type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly 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.

Ectodermal dysplasia/short stature syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectodermal dysplasia/short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, idiopathic, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, idiopathic, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short-sleeper Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short-sleeper phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short-rib thoracic dysplasia 11 with or without polydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

short QT syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the short QT 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.

Microcephaly, short stature, and impaired glucose metabolism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, short stature, and impaired glucose metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital short bowel syndrome, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital short bowel syndrome, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short rib polydactyly syndrome 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short rib polydactyly syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short rib polydactyly syndrome 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short rib polydactyly syndrome 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short-rib thoracic dysplasia 10 with or without polydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

SHORT syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the SHORT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Brachyrachia (short spine dysplasia) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Brachyrachia (short spine dysplasia) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short-rib thoracic dysplasia 3 with or without polydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short-rib thoracic dysplasia 3 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Yakut short stature syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Yakut short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondylometaepiphyseal dysplasia short limb-hand type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondylometaepiphyseal dysplasia short limb-hand type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

short-chain collagen trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the short-chain collagen trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

short-chain collagen trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the short-chain collagen trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS 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.

Short QT Syndrome 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Short QT Syndrome 1 from the curated CTD Gene-Disease Associations dataset.

Short QT Syndrome 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Short QT Syndrome 3 from the curated CTD Gene-Disease Associations dataset.

Short QT Syndrome 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Short QT Syndrome 2 from the curated CTD Gene-Disease Associations dataset.

Short Stature, Idiopathic, Autosomal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Short Stature, Idiopathic, Autosomal from the curated CTD Gene-Disease Associations dataset.

Short Stature, Idiopathic, X-Linked Gene Set

From CTD Gene-Disease Associations

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

Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type from the curated CTD Gene-Disease Associations dataset.

Short Rib-Polydactyly Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Short Rib-Polydactyly Syndrome from the curated CTD Gene-Disease Associations dataset.

Short chain Acyl CoA dehydrogenase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Short chain Acyl CoA dehydrogenase deficiency from the curated CTD Gene-Disease Associations dataset.

SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY from the curated CTD Gene-Disease Associations dataset.

short bowel syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

short stature Gene Set

From GAD Gene-Disease Associations

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

idiopathic short stature Gene Set

From GAD Gene-Disease Associations

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

multiple organ failure; short bowel syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple organ failure; short bowel syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

short Gene Set

From GeneRIF Biological Term Annotations

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

16478745-SuppTable1-short Gene Set

From GeneSigDB Published Gene Signatures

genes in signature reported in the publication with PubMedID 16478745-SuppTable1-short from the GeneSigDB Published Gene Signatures dataset.

short-chain fatty acid metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the short-chain fatty acid metabolic process biological process from the curated GO Biological Process Annotations dataset.

short-chain fatty acid transport Gene Set

From GO Biological Process Annotations

genes participating in the short-chain fatty acid transport biological process from the curated GO Biological Process Annotations dataset.

short-chain fatty acid biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the short-chain fatty acid biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

short-chain fatty acid import Gene Set

From GO Biological Process Annotations

genes participating in the short-chain fatty acid import biological process from the curated GO Biological Process Annotations dataset.

short-chain fatty acid catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the short-chain fatty acid catabolic process biological process from the curated GO Biological Process Annotations dataset.

short-chain collagen trimer Gene Set

From GO Cellular Component Annotations

proteins localized to the short-chain collagen trimer cellular component from the curated GO Cellular Component Annotations dataset.

short-chain fatty acid uptake transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the short-chain fatty acid uptake transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

short-chain carboxylesterase activity Gene Set

From GO Molecular Function Annotations

genes performing the short-chain carboxylesterase activity molecular function from the curated GO Molecular Function Annotations dataset.

short-chain fatty acid transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the short-chain fatty acid transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

Hypertension risk in short sleep duration Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Hypertension risk in short sleep duration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

short attention span Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the short attention span phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

short distal phalanx of finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

moderately short stature Gene Set

From HPO Gene-Disease Associations

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

short nasal bridge Gene Set

From HPO Gene-Disease Associations

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

short chordae tendineae of the tricuspid valve Gene Set

From HPO Gene-Disease Associations

genes associated with the short chordae tendineae of the tricuspid valve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short nose Gene Set

From HPO Gene-Disease Associations

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

short 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short 5th toe Gene Set

From HPO Gene-Disease Associations

genes associated with the short 5th toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short 4th toe Gene Set

From HPO Gene-Disease Associations

genes associated with the short 4th toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short diaphyses Gene Set

From HPO Gene-Disease Associations

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

short metacarpals with rounded proximal ends Gene Set

From HPO Gene-Disease Associations

genes associated with the short metacarpals with rounded proximal ends phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short 1st metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the short 1st metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short femoral neck Gene Set

From HPO Gene-Disease Associations

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

short digit Gene Set

From HPO Gene-Disease Associations

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

relatively short spine Gene Set

From HPO Gene-Disease Associations

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

short sacroiliac notch Gene Set

From HPO Gene-Disease Associations

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

short chordae tendineae of the mitral valve Gene Set

From HPO Gene-Disease Associations

genes associated with the short chordae tendineae of the mitral valve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short columella Gene Set

From HPO Gene-Disease Associations

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

short nail Gene Set

From HPO Gene-Disease Associations

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

short stature Gene Set

From HPO Gene-Disease Associations

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

short fourth metatarsal Gene Set

From HPO Gene-Disease Associations

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

short humerus Gene Set

From HPO Gene-Disease Associations

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

mesomelic short stature Gene Set

From HPO Gene-Disease Associations

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

short middle phalanx of finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short middle phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short philtrum Gene Set

From HPO Gene-Disease Associations

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

short metatarsal Gene Set

From HPO Gene-Disease Associations

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

short umbilical cord Gene Set

From HPO Gene-Disease Associations

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

short upper lip Gene Set

From HPO Gene-Disease Associations

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

short distal phalanx of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short palpebral fissure Gene Set

From HPO Gene-Disease Associations

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

short femur Gene Set

From HPO Gene-Disease Associations

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

short phalanx of the thumb Gene Set

From HPO Gene-Disease Associations

genes associated with the short phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short attention span Gene Set

From HPO Gene-Disease Associations

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

short 5th metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the short 5th metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short middle phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short proximal phalanx of finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short proximal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short chin Gene Set

From HPO Gene-Disease Associations

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

short thorax Gene Set

From HPO Gene-Disease Associations

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

short mandibular rami Gene Set

From HPO Gene-Disease Associations

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

short lingual frenulum Gene Set

From HPO Gene-Disease Associations

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

disproportionate short stature Gene Set

From HPO Gene-Disease Associations

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

short 3rd metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the short 3rd metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short palm Gene Set

From HPO Gene-Disease Associations

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

short mandibular condyles Gene Set

From HPO Gene-Disease Associations

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

short 2nd toe Gene Set

From HPO Gene-Disease Associations

genes associated with the short 2nd toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short proximal phalanx of thumb Gene Set

From HPO Gene-Disease Associations

genes associated with the short proximal phalanx of thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mild short stature Gene Set

From HPO Gene-Disease Associations

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

short middle phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short neck Gene Set

From HPO Gene-Disease Associations

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

severe short-limb dwarfism Gene Set

From HPO Gene-Disease Associations

genes associated with the severe short-limb dwarfism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short phalanx of finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short foot Gene Set

From HPO Gene-Disease Associations

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

short distal phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short ribs Gene Set

From HPO Gene-Disease Associations

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

short proximal phalanx of hallux Gene Set

From HPO Gene-Disease Associations

genes associated with the short proximal phalanx of hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short ear Gene Set

From HPO Gene-Disease Associations

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

proportionate short stature Gene Set

From HPO Gene-Disease Associations

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

short toe Gene Set

From HPO Gene-Disease Associations

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

short thumb Gene Set

From HPO Gene-Disease Associations

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

short iliac bones Gene Set

From HPO Gene-Disease Associations

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

short lower limbs Gene Set

From HPO Gene-Disease Associations

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

short distal phalanx of the thumb Gene Set

From HPO Gene-Disease Associations

genes associated with the short distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short phalanx of hallux Gene Set

From HPO Gene-Disease Associations

genes associated with the short phalanx of hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short hard palate Gene Set

From HPO Gene-Disease Associations

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

short nasal septum Gene Set

From HPO Gene-Disease Associations

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

short distal phalanx of toe Gene Set

From HPO Gene-Disease Associations

genes associated with the short distal phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short metacarpal Gene Set

From HPO Gene-Disease Associations

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

short distal phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short long bone Gene Set

From HPO Gene-Disease Associations

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

short sternum Gene Set

From HPO Gene-Disease Associations

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

short 4th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short stepped shuffling gait Gene Set

From HPO Gene-Disease Associations

genes associated with the short stepped shuffling gait phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short distal phalanx of the 4th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short tibia Gene Set

From HPO Gene-Disease Associations

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

short 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short 4th metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the short 4th metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe short stature Gene Set

From HPO Gene-Disease Associations

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

short tubular bones (hand) Gene Set

From HPO Gene-Disease Associations

genes associated with the short tubular bones (hand) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short clavicles Gene Set

From HPO Gene-Disease Associations

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

short middle phalanx of toe Gene Set

From HPO Gene-Disease Associations

genes associated with the short middle phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short first metatarsal Gene Set

From HPO Gene-Disease Associations

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

short finger Gene Set

From HPO Gene-Disease Associations

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

short hallux Gene Set

From HPO Gene-Disease Associations

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

Short Bowel Syndrome Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Short Bowel Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Short hematopoietin receptor, family 1, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Short hematopoietin receptor, family 1, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Short hematopoietin receptor, family 2, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Short hematopoietin receptor, family 2, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Short-chain dehydrogenase/reductase, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Short-chain dehydrogenase/reductase, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Short-chain dehydrogenase/reductase SDR Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Short-chain dehydrogenase/reductase SDR protein domain from the InterPro Predicted Protein Domain Annotations dataset.

short nasal bone Gene Set

From MPO Gene-Phenotype Associations

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

short frontal bone Gene Set

From MPO Gene-Phenotype Associations

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

short perineum Gene Set

From MPO Gene-Phenotype Associations

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

short tail Gene Set

From MPO Gene-Phenotype Associations

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

short photoreceptor inner segment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short photoreceptor inner segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short squamosal bone Gene Set

From MPO Gene-Phenotype Associations

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

short malleus manubrium Gene Set

From MPO Gene-Phenotype Associations

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

short metestrus Gene Set

From MPO Gene-Phenotype Associations

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

short metatarsal bones Gene Set

From MPO Gene-Phenotype Associations

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

short diestrus Gene Set

From MPO Gene-Phenotype Associations

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

short photoreceptor outer segment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short photoreceptor outer segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short vertebral body Gene Set

From MPO Gene-Phenotype Associations

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

short zygomatic bone Gene Set

From MPO Gene-Phenotype Associations

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

short fibula Gene Set

From MPO Gene-Phenotype Associations

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

short palate Gene Set

From MPO Gene-Phenotype Associations

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

short premaxilla Gene Set

From MPO Gene-Phenotype Associations

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

short excitatory postsynaptic current decay time Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short excitatory postsynaptic current decay time phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short proestrus Gene Set

From MPO Gene-Phenotype Associations

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

short ureter Gene Set

From MPO Gene-Phenotype Associations

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

short humerus Gene Set

From MPO Gene-Phenotype Associations

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

short uterine horn Gene Set

From MPO Gene-Phenotype Associations

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

short tibia Gene Set

From MPO Gene-Phenotype Associations

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

short radius Gene Set

From MPO Gene-Phenotype Associations

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

short ulna Gene Set

From MPO Gene-Phenotype Associations

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

short stride length Gene Set

From MPO Gene-Phenotype Associations

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

short vibrissae Gene Set

From MPO Gene-Phenotype Associations

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

short umbilical cord Gene Set

From MPO Gene-Phenotype Associations

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

short malleus Gene Set

From MPO Gene-Phenotype Associations

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

short hair Gene Set

From MPO Gene-Phenotype Associations

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

short lumbar vertebrae Gene Set

From MPO Gene-Phenotype Associations

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

short estrous cycle Gene Set

From MPO Gene-Phenotype Associations

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

short mandible Gene Set

From MPO Gene-Phenotype Associations

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

short rostral-caudal axis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short rostral-caudal axis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short cochlear hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short cochlear hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short maxilla Gene Set

From MPO Gene-Phenotype Associations

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

short kidney papilla Gene Set

From MPO Gene-Phenotype Associations

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

short outer hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short outer hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short endolymphatic duct Gene Set

From MPO Gene-Phenotype Associations

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

short oviduct Gene Set

From MPO Gene-Phenotype Associations

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

short presphenoid bone Gene Set

From MPO Gene-Phenotype Associations

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

short ribs Gene Set

From MPO Gene-Phenotype Associations

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

short snout Gene Set

From MPO Gene-Phenotype Associations

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

short vertebral column Gene Set

From MPO Gene-Phenotype Associations

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

short nails Gene Set

From MPO Gene-Phenotype Associations

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

short cochlear outer hair cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short cochlear outer hair cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short gestation period Gene Set

From MPO Gene-Phenotype Associations

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

short sternum Gene Set

From MPO Gene-Phenotype Associations

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

short neck Gene Set

From MPO Gene-Phenotype Associations

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

short femur Gene Set

From MPO Gene-Phenotype Associations

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

short inner hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short inner hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short sperm flagellum Gene Set

From MPO Gene-Phenotype Associations

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

short limbs Gene Set

From MPO Gene-Phenotype Associations

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

short metacarpal bones Gene Set

From MPO Gene-Phenotype Associations

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

short incisors Gene Set

From MPO Gene-Phenotype Associations

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

short scapula Gene Set

From MPO Gene-Phenotype Associations

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

short scala media Gene Set

From MPO Gene-Phenotype Associations

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

short trachea Gene Set

From MPO Gene-Phenotype Associations

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

short estrus Gene Set

From MPO Gene-Phenotype Associations

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

short syndrome Gene Set

From OMIM Gene-Disease Associations

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

short-rib thoracic dysplasia 10 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 4 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 4 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

[short sleeper] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [short sleeper] 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.

ectodermal dysplasia/short stature syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia/short stature syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 6 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 6 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 7 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 7 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

spondylometaepiphyseal dysplasia, short limb-hand type Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondylometaepiphyseal dysplasia, short limb-hand type phenotype from the curated OMIM Gene-Disease Associations dataset.

short stature Gene Set

From OMIM Gene-Disease Associations

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

short-rib thoracic dysplasia 11 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital short bowel syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital short bowel syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

short qt syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the short qt syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

short qt syndrome 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the short qt syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

short qt syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the short qt syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

?retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?retinal dystrophy, juvenile cataracts, and short stature 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.

short-rib thoracic dysplasia 9 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 9 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

acyl-coa dehydrogenase, short-chain, deficiency of Gene Set

From OMIM Gene-Disease Associations

genes associated with the acyl-coa dehydrogenase, short-chain, deficiency of phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, short stature, and impaired glucose metabolism Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, short stature, and impaired glucose metabolism phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 3 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 3 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

osteochondritis dissecans, short stature, and early-onset osteoarthritis Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteochondritis dissecans, short stature, and early-onset osteoarthritis phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 8 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 8 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

short stature with microcephaly and distinctive facies Gene Set

From OMIM Gene-Disease Associations

genes associated with the short stature with microcephaly and distinctive facies phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 2 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 2 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

short stature, idiopathic familial Gene Set

From OMIM Gene-Disease Associations

genes associated with the short stature, idiopathic familial phenotype from the curated OMIM Gene-Disease Associations dataset.

short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 5 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 5 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated OMIM Gene-Disease Associations dataset.

Thyroid hormone metabolism, abnormal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thyroid hormone metabolism, abnormal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Reflex, Abnormal Gene Set

From CTD Gene-Disease Associations

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

Neutrophil Chemotactic Response, Abnormal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neutrophil Chemotactic Response, Abnormal from the curated CTD Gene-Disease Associations dataset.

Thyroid Hormone Metabolism, Abnormal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thyroid Hormone Metabolism, Abnormal from the curated CTD Gene-Disease Associations dataset.

abnormal retinal correspondence Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

abnormal splicing Gene Set

From GAD Gene-Disease Associations

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

ekg, abnormal Gene Set

From GAD Gene-Disease Associations

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

ekg, abnormal; brugada syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ekg, abnormal; brugada syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormal urogenital development Gene Set

From GAD Gene-Disease Associations

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

abnormal fibrin polymerization and thrombophilia Gene Set

From GAD Gene-Disease Associations

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

abnormal Gene Set

From GeneRIF Biological Term Annotations

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

abnormal cannabidiol Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the abnormal cannabidiol ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

abnormal eye physiology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal renal physiology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal gallbladder morphology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal gallbladder physiology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal intraocular pressure Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal eating behavior Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal thrombosis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal leukocyte count Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal iris pigmentation Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal bone structure Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal serum iron Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal emotion/affect behavior Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal emotion/affect behavior phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal bleeding Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal atrioventricular conduction Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal hair quantity Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal nervous system electrophysiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal nervous system electrophysiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal male reproductive system physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal male reproductive system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal external genitalia Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal ekg Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal axial skeleton morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal axial skeleton morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal immunoglobulin level Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal monocyte count Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal neutrophil cell number Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal neutrophil cell number 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.

abnormal platelet count Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal aggressive, impulsive or violent behavior Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal aggressive, impulsive or violent behavior phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

acquired abnormal hair pattern Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the acquired abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal glomerular filtration rate Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal glomerular filtration rate phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal eye morphology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal testosterone level Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal joint morphology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal motor neuron morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal motor neuron morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal biliary tract morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal biliary tract morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal neuron morphology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal genital system morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal genital system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal appendicular skeleton morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal appendicular skeleton morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal cortical bone morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal cortical bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal electrophysiology of sinoatrial node origin Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal electrophysiology of sinoatrial node origin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal respiratory system morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal respiratory system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal number of teeth Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal number of teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal hair pattern Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal circulating creatinine level Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal circulating creatinine level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal peripheral nervous system morphology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal peripheral nervous system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal autonomic nervous system physiology Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal autonomic nervous system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormal platelet function Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal muscle tone Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal diaphysis morphology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal spermatogenesis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal hemoglobin Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal internal genitalia Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal glucose homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal renal morphology Gene Set

From GWASdb SNP-Phenotype Associations

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

abnormal dermatoglyphics Gene Set

From HPO Gene-Disease Associations

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

abnormal gallbladder morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal ossification of hand bones Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal ossification of hand bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal bone structure Gene Set

From HPO Gene-Disease Associations

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

abnormal branching pattern of the aortic arch Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal branching pattern of the aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal motor nerve conduction velocity Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal motor nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal maternal serum screening Gene Set

From HPO Gene-Disease Associations

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

abnormal rod and cone electroretinograms Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal rod and cone electroretinograms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal albumin level Gene Set

From HPO Gene-Disease Associations

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

abnormal enchondral ossification Gene Set

From HPO Gene-Disease Associations

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

abnormal number of vertebrae Gene Set

From HPO Gene-Disease Associations

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

abnormal platelet membrane protein expression Gene Set

From HPO Gene-Disease Associations

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

abnormal mitochondria in muscle tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal mitochondria in muscle tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal male reproductive system physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal male reproductive system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal placental size Gene Set

From HPO Gene-Disease Associations

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

abnormal central microtubular pair morphology of respiratory motile cilia Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal central microtubular pair morphology of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal platelet granules Gene Set

From HPO Gene-Disease Associations

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

abnormal subcutaneous fat tissue distribution Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal subcutaneous fat tissue distribution phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal electroretinogram Gene Set

From HPO Gene-Disease Associations

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

abnormal lung lobation Gene Set

From HPO Gene-Disease Associations

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

abnormal flash visual evoked potentials Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal flash visual evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal peripheral nervous system synaptic transmission Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal peripheral nervous system synaptic transmission phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal urine phosphate concentration Gene Set

From HPO Gene-Disease Associations

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

abnormal drinking behavior Gene Set

From HPO Gene-Disease Associations

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

abnormal sperm motility Gene Set

From HPO Gene-Disease Associations

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

abnormal fear/anxiety-related behavior Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal fear/anxiety-related behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal renal corticomedullary differentiation Gene Set

From HPO Gene-Disease Associations

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

abnormal humeral ossification Gene Set

From HPO Gene-Disease Associations

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

abnormal delayed hypersensitivity skin test Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal delayed hypersensitivity skin test phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal upper motor neuron morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal upper motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal protein n-linked glycosylation Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal protein n-linked glycosylation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal echocardiogram Gene Set

From HPO Gene-Disease Associations

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

abnormal serum ferritin Gene Set

From HPO Gene-Disease Associations

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

abnormal female reproductive system physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal female reproductive system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal hypothalamus morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal axial skeleton morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal calcification of the carpal bones Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal calcification of the carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal testosterone level Gene Set

From HPO Gene-Disease Associations

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

abnormal peripheral myelination Gene Set

From HPO Gene-Disease Associations

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

abnormal speech discrimination Gene Set

From HPO Gene-Disease Associations

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

abnormal genital system morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal morphology of bones of the lower limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal morphology of bones of the lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal liver function tests during pregnancy Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal liver function tests during pregnancy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal cortical bone morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal hypothalamus physiology Gene Set

From HPO Gene-Disease Associations

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

abnormal trabecular bone morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal electrophysiology of sinoatrial node origin Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal electrophysiology of sinoatrial node origin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal metacarpal morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal t3/t4 ratio Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal t3/t4 ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal glycosylation Gene Set

From HPO Gene-Disease Associations

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

abnormal iris vasculature Gene Set

From HPO Gene-Disease Associations

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

abnormal pupillary function Gene Set

From HPO Gene-Disease Associations

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

abnormal posturing Gene Set

From HPO Gene-Disease Associations

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

abnormal natural killer cell physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal natural killer cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal external genitalia Gene Set

From HPO Gene-Disease Associations

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

abnormal immunoglobulin level Gene Set

From HPO Gene-Disease Associations

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

congenital abnormal hair pattern Gene Set

From HPO Gene-Disease Associations

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

abnormal nervous system electrophysiology Gene Set

From HPO Gene-Disease Associations

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

abnormal autonomic nervous system physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal autonomic nervous system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal monocyte count Gene Set

From HPO Gene-Disease Associations

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

abnormal atrial arrangement Gene Set

From HPO Gene-Disease Associations

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

abnormal morphology of ulna Gene Set

From HPO Gene-Disease Associations

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

abnormal circulating renin Gene Set

From HPO Gene-Disease Associations

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

abnormal retinal folds Gene Set

From HPO Gene-Disease Associations

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

abnormal pancreas size Gene Set

From HPO Gene-Disease Associations

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

abnormal urine sodium concentration Gene Set

From HPO Gene-Disease Associations

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

abnormal vestibulo-ocular reflex Gene Set

From HPO Gene-Disease Associations

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

abnormal vertebral pedicle morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal tendon morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal glucose homeostasis Gene Set

From HPO Gene-Disease Associations

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

abnormal leukocyte count Gene Set

From HPO Gene-Disease Associations

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

abnormal tarsal ossification Gene Set

From HPO Gene-Disease Associations

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

abnormal spermatogenesis Gene Set

From HPO Gene-Disease Associations

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

abnormal size of pituitary gland Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal size of pituitary gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal urine potassium concentration Gene Set

From HPO Gene-Disease Associations

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

abnormal synaptic transmission at the neuromuscular junction Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal synaptic transmission at the neuromuscular junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal peripheral nervous system morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal peripheral nervous system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal pupillary light reflex Gene Set

From HPO Gene-Disease Associations

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

abnormal pyramidal signs Gene Set

From HPO Gene-Disease Associations

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

abnormal biliary tract morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal pigmentation of the oral mucosa Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal pigmentation of the oral mucosa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal hair pattern Gene Set

From HPO Gene-Disease Associations

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

abnormal number of incisors Gene Set

From HPO Gene-Disease Associations

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

abnormal localization of kidney Gene Set

From HPO Gene-Disease Associations

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

abnormal elasticity of skin Gene Set

From HPO Gene-Disease Associations

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

abnormal platelet volume Gene Set

From HPO Gene-Disease Associations

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

abnormal vas deferens morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal muscle tone Gene Set

From HPO Gene-Disease Associations

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

abnormal lower motor neuron morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal lower motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal ciliary motility Gene Set

From HPO Gene-Disease Associations

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

abnormal atrioventricular conduction Gene Set

From HPO Gene-Disease Associations

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

abnormal metatarsal ossification Gene Set

From HPO Gene-Disease Associations

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

abnormal st segment Gene Set

From HPO Gene-Disease Associations

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

abnormal sweat homeostasis Gene Set

From HPO Gene-Disease Associations

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

abnormal nasal base Gene Set

From HPO Gene-Disease Associations

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

abnormal pelvis bone ossification Gene Set

From HPO Gene-Disease Associations

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

abnormal sperm morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal ossification of the pubic bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal ossification of the pubic bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal isoelectric focusing of serum transferrin Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal isoelectric focusing of serum transferrin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal hemoglobin Gene Set

From HPO Gene-Disease Associations

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

abnormal morphology of bones of the upper limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal morphology of bones of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal nasal morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal ossification involving the femoral head and neck Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal ossification involving the femoral head and neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal concentration of calcium in blood Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal concentration of calcium in blood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal emotion/affect behavior Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal emotion/affect behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal epiphyseal ossification Gene Set

From HPO Gene-Disease Associations

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

abnormal urine cytology Gene Set

From HPO Gene-Disease Associations

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

abnormal palmar dermatoglyphics Gene Set

From HPO Gene-Disease Associations

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

abnormal neuron morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal csf lactate level Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal csf lactate level 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.

abnormal joint morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal vertebral segmentation and fusion Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal vertebral segmentation and fusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal internal genitalia Gene Set

From HPO Gene-Disease Associations

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

abnormal oral glucose tolerance Gene Set

From HPO Gene-Disease Associations

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

abnormal bone collagen fibril morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal bone collagen fibril morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal delivery Gene Set

From HPO Gene-Disease Associations

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

abnormal middle ear reflexes Gene Set

From HPO Gene-Disease Associations

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

abnormal mitochondrial morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal cervical curvature Gene Set

From HPO Gene-Disease Associations

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

abnormal bleeding Gene Set

From HPO Gene-Disease Associations

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

abnormal myelination Gene Set

From HPO Gene-Disease Associations

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

abnormal mitochondrial shape Gene Set

From HPO Gene-Disease Associations

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

abnormal auditory evoked potentials Gene Set

From HPO Gene-Disease Associations

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

abnormal activity of mitochondrial respiratory chain Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal activity of mitochondrial respiratory chain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal location of ears Gene Set

From HPO Gene-Disease Associations

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

abnormal cns myelination Gene Set

From HPO Gene-Disease Associations

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

abnormal eye physiology Gene Set

From HPO Gene-Disease Associations

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

abnormal renal physiology Gene Set

From HPO Gene-Disease Associations

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

abnormal synaptic transmission Gene Set

From HPO Gene-Disease Associations

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

abnormal eating behavior Gene Set

From HPO Gene-Disease Associations

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

abnormal atrioventricular connection Gene Set

From HPO Gene-Disease Associations

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

abnormal ventriculo-arterial connection Gene Set

From HPO Gene-Disease Associations

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

abnormal anterior horn cell morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal anterior horn cell morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal germ cell morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal upper to lower segment ratio Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal upper to lower segment ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal form of the vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal form of the vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal biliary tract physiology Gene Set

From HPO Gene-Disease Associations

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

abnormal urine output Gene Set

From HPO Gene-Disease Associations

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

abnormal blistering of the skin Gene Set

From HPO Gene-Disease Associations

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

abnormal diaphysis morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal cholesterol homeostasis Gene Set

From HPO Gene-Disease Associations

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

abnormal urine citrate concentration Gene Set

From HPO Gene-Disease Associations

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

abnormal size of the palpebral fissures Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal size of the palpebral fissures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal hand morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal hair quantity Gene Set

From HPO Gene-Disease Associations

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

abnormal anatomic location of the heart Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal anatomic location of the heart phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal iron deposition in mitochondria Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal iron deposition in mitochondria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal morphology of forearm bone Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal morphology of forearm bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal circulating aldosterone Gene Set

From HPO Gene-Disease Associations

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

abnormal male germ cell morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal male germ cell morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal platelet morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal circulating creatinine level Gene Set

From HPO Gene-Disease Associations

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

abnormal platelet function Gene Set

From HPO Gene-Disease Associations

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

abnormal large intestine physiology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal large intestine physiology 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.

abnormal urine chloride concentration Gene Set

From HPO Gene-Disease Associations

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

abnormal vascular physiology Gene Set

From HPO Gene-Disease Associations

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

abnormal vertebral ossification Gene Set

From HPO Gene-Disease Associations

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

abnormal renal morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal heart morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal hair laboratory examination Gene Set

From HPO Gene-Disease Associations

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

abnormal retinal pigmentation Gene Set

From HPO Gene-Disease Associations

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

abnormal shape of the palpebral fissure Gene Set

From HPO Gene-Disease Associations

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

abnormal lymphocyte count Gene Set

From HPO Gene-Disease Associations

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

abnormal conjugate eye movement Gene Set

From HPO Gene-Disease Associations

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

abnormal autonomic nervous system morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal autonomic nervous system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal pulmonary lymphatics Gene Set

From HPO Gene-Disease Associations

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

abnormal bone ossification Gene Set

From HPO Gene-Disease Associations

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

abnormal pattern of respiration Gene Set

From HPO Gene-Disease Associations

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

abnormal protein glycosylation Gene Set

From HPO Gene-Disease Associations

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

abnormal hair whorl Gene Set

From HPO Gene-Disease Associations

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

abnormal connection of the cardiac segments Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal connection of the cardiac segments phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal cartilage collagen Gene Set

From HPO Gene-Disease Associations

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

abnormal umbilical stump bleeding Gene Set

From HPO Gene-Disease Associations

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

abnormal social behavior Gene Set

From HPO Gene-Disease Associations

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

abnormal cortical gyration Gene Set

From HPO Gene-Disease Associations

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

abnormal serum iron Gene Set

From HPO Gene-Disease Associations

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

abnormal number of permanent teeth Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal number of permanent teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal sex determination Gene Set

From HPO Gene-Disease Associations

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

abnormal prolactin level Gene Set

From HPO Gene-Disease Associations

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

abnormal respiratory system morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal number of teeth Gene Set

From HPO Gene-Disease Associations

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

abnormal respiratory epithelium morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal axonemal organization of respiratory motile cilia Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal axonemal organization of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal foot bone ossification Gene Set

From HPO Gene-Disease Associations

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

abnormal shape of the radius Gene Set

From HPO Gene-Disease Associations

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

abnormal neutrophil cell number Gene Set

From HPO Gene-Disease Associations

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

abnormal platelet count Gene Set

From HPO Gene-Disease Associations

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

abnormal eye morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal cone-mediated electroretinogram Gene Set

From HPO Gene-Disease Associations

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

abnormal basal ganglia mri signal intensity Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal basal ganglia mri signal intensity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal respiratory motile cilium morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal sensory nerve conduction velocity Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal sensory nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal muscle glycogen content Gene Set

From HPO Gene-Disease Associations

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

abnormal appendicular skeleton morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal hand bone ossification Gene Set

From HPO Gene-Disease Associations

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

abnormal number of erythroid precursors Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal number of erythroid precursors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal respiratory motile cilium physiology Gene Set

From HPO Gene-Disease Associations

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

abnormal urine magnesium concentration Gene Set

From HPO Gene-Disease Associations

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

abnormal rapid eye movement (rem) sleep Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal rapid eye movement (rem) sleep phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal nerve conduction velocity Gene Set

From HPO Gene-Disease Associations

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

abnormal thrombosis Gene Set

From HPO Gene-Disease Associations

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

abnormal glucose tolerance Gene Set

From HPO Gene-Disease Associations

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

abnormal ekg Gene Set

From HPO Gene-Disease Associations

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

abnormal levels of creatine kinase in blood Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal levels of creatine kinase in blood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal ejaculation Gene Set

From HPO Gene-Disease Associations

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

abnormal aggressive, impulsive or violent behavior Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal aggressive, impulsive or violent behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal motor neuron morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal urinary electrolyte concentration Gene Set

From HPO Gene-Disease Associations

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

abnormal finger flexion creases Gene Set

From HPO Gene-Disease Associations

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

abnormal metaphyseal trabeculation Gene Set

From HPO Gene-Disease Associations

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

abnormal umbilical cord blood vessels Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal umbilical cord blood vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal head movements Gene Set

From HPO Gene-Disease Associations

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

acquired abnormal hair pattern Gene Set

From HPO Gene-Disease Associations

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

abnormal facility in opposing the shoulders Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal facility in opposing the shoulders phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal migration of corneal endothelium Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal migration of corneal endothelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal gallbladder physiology Gene Set

From HPO Gene-Disease Associations

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

abnormal intraocular pressure Gene Set

From HPO Gene-Disease Associations

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

abnormal shape of the frontal region Gene Set

From HPO Gene-Disease Associations

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

abnormal iris pigmentation Gene Set

From HPO Gene-Disease Associations

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

abnormal urinary sulfate concentration Gene Set

From HPO Gene-Disease Associations

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

abnormal morphology of the radius Gene Set

From HPO Gene-Disease Associations

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

abnormal rib ossification Gene Set

From HPO Gene-Disease Associations

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

abnormal glomerular filtration rate Gene Set

From HPO Gene-Disease Associations

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

abnormal sternal ossification Gene Set

From HPO Gene-Disease Associations

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

abnormal shape of the occiput Gene Set

From HPO Gene-Disease Associations

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

abnormal involuntary eye movements Gene Set

From HPO Gene-Disease Associations

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

abnormal metaphyseal vascular invasion Gene Set

From HPO Gene-Disease Associations

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

abnormal enzyme/coenzyme activity Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal enzyme/coenzyme activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal cartilage morphology Gene Set

From HPO Gene-Disease Associations

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

abnormal peripheral action potential amplitude Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal peripheral action potential amplitude phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Reflex, Abnormal Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Spindle assembly abnormal protein 6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Spindle assembly abnormal protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

DMRT/protein doublesex/protein male abnormal 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the DMRT/protein doublesex/protein male abnormal 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Protein male abnormal 21-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Protein male abnormal 21-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Abnormal spindle-like microcephaly-associated protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Abnormal spindle-like microcephaly-associated protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal clitoris morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal male genitalia morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal lung volume Gene Set

From MPO Gene-Phenotype Associations

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

abnormal basilar membrane morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal neural fold elevation formation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural fold elevation formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal sensory capabilities/reflexes/nociception Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal sensory capabilities/reflexes/nociception phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal behavioral response to anesthetic Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal behavioral response to anesthetic phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal trigeminal ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal auditory brainstem response waveform shape Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal auditory brainstem response waveform shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal photoreceptor layer morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal bradykinin level Gene Set

From MPO Gene-Phenotype Associations

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

abnormal fetal derived definitive erythrocyte cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal fetal derived definitive erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal paravertebral ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal nasal cavity morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal primary sex determination Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal primary sex determination phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hippocampus stratum lacunosum morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal gallbladder morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal ectomesenchyme morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal male urethra morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal bone marrow cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal bone marrow cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal zona glomerulosa morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal ear development Gene Set

From MPO Gene-Phenotype Associations

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

abnormal surfactant secretion Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cerebellum fastigial nucleus morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal social/conspecific interaction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal social/conspecific interaction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hippocampus size Gene Set

From MPO Gene-Phenotype Associations

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

abnormal tooth morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal neutrophil differentiation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal vomer bone morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal endplate potential Gene Set

From MPO Gene-Phenotype Associations

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

abnormal sagittal suture morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal semicircular canal morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal estrous cycle Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cd4-positive t cell differentiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cd4-positive t cell differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neuron differentiation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal long bone metaphysis morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal testis size Gene Set

From MPO Gene-Phenotype Associations

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

abnormal vascular endothelial cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal sympathetic neuron innervation pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal sympathetic neuron innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal melanosome transport Gene Set

From MPO Gene-Phenotype Associations

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

abnormal inferior colliculus morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal tongue muscle morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal inner nuclear layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal inner nuclear layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal keratinocyte physiology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal behavioral response to methamphetamine Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal behavioral response to methamphetamine phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal auditory brainstem response Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal auditory brainstem response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal macrophage derived foam cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal macrophage derived foam cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal heart left atrium weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal heart left atrium weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal malleus morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal scala vestibuli morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal pupillary reflex Gene Set

From MPO Gene-Phenotype Associations

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

abnormal interdigital cell death Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal interdigital cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal schwann cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal posterior definitive endoderm morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal keratinocyte morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal renal protein reabsorption Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal renal protein reabsorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal habenula morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal urine antidiuretic hormone level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal urine antidiuretic hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal embryonic tissue morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal laryngeal mucosa morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal plasma membrane morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal circulating angiotensinogen level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal circulating angiotensinogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal b cell apoptosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal b cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal corneocyte envelope morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal primordial ovarian follicle number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal primordial ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal prostate gland dorsolateral lobe morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal prostate gland dorsolateral lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal vestibular nerve morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal melanocyte morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cochlear inner hair cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cochlear inner hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal parametrial fat pad morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal effector t cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal urine aldosterone level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal urine aldosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal roof plate morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal bone healing Gene Set

From MPO Gene-Phenotype Associations

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

abnormal rhombomere 4 morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal rhombomere 4 morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal heart right ventricle size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal heart right ventricle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal snout morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal optic disc morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal parasympathetic ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal blinking Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blinking 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 circulating interleukin-1 alpha level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal circulating interleukin-1 alpha level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal thyroid gland development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal thyroid gland development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal efferent ductules of testis morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal efferent ductules of testis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal periocular mesenchyme morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal purkinje cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal purkinje cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal circulating pancreatic peptide level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal circulating pancreatic peptide level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal frontonasal prominence morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal gas homeostasis Gene Set

From MPO Gene-Phenotype Associations

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

abnormal intestinal mucosa morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal dermis papillary layer morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hair shaft morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cellular replicative senescence Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cellular replicative senescence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal throat morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal nasolacrimal duct morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal first pharyngeal arch morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal loop of henle descending limb morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal loop of henle descending limb morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal triiodothyronine level Gene Set

From MPO Gene-Phenotype Associations

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

abnormal visual acuity Gene Set

From MPO Gene-Phenotype Associations

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

abnormal circulating sulfate level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal circulating sulfate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal parturition Gene Set

From MPO Gene-Phenotype Associations

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

abnormal scala tympani morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal external urethral orifice morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal male reproductive gland physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal male reproductive gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal chorioallantoic fusion Gene Set

From MPO Gene-Phenotype Associations

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

abnormal purkinje cell dendrite morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal lens development Gene Set

From MPO Gene-Phenotype Associations

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

abnormal pituitary diverticulum morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal arteriole morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal outer hair cell stereociliary bundle morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal outer hair cell stereociliary bundle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal pancreatic endocrine progenitor cell proliferation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal pancreatic endocrine progenitor cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cd4-positive, cd25-positive, alpha-beta regulatory t cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cd4-positive, cd25-positive, alpha-beta regulatory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal rosenthal canal morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal pr interval Gene Set

From MPO Gene-Phenotype Associations

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

abnormal enterocyte apoptosis Gene Set

From MPO Gene-Phenotype Associations

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

abnormal renal glomerulus basement membrane thickness Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal renal glomerulus basement membrane thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal superior vagus ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal melanoblast morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal urinary bladder weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal urinary bladder weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal single cell response threshold Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal single cell response threshold phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal dermis reticular layer morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal body height Gene Set

From MPO Gene-Phenotype Associations

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

abnormal kidney epithelial cell primary cilium physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal kidney epithelial cell primary cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal optic stalk morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal neural tube mantle layer morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural tube mantle layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal posterior cardinal vein morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal renal tubule epithelial cell primary cilium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal renal tubule epithelial cell primary cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal intramembranous bone ossification Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal intramembranous bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ear distance/ position Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ear distance/ position phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal mitochondrion morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal maxillary sinus morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal otic vesicle development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal otic vesicle development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal brown adipose tissue physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal brown adipose tissue physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal lymph node b cell domain morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal lymph node b cell domain morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal circulating lactate dehydrogenase level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal circulating lactate dehydrogenase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal plasmacytoid dendritic cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal plasmacytoid dendritic cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal urinary bladder morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal rod cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal digestive system development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal digestive system development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal auditory summating potential Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal auditory summating potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal paired-pulse inhibition Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal paired-pulse inhibition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal aortic arch and aortic arch branch attachment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal aortic arch and aortic arch branch attachment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal ganglion cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal postnatal growth Gene Set

From MPO Gene-Phenotype Associations

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

abnormal brain development Gene Set

From MPO Gene-Phenotype Associations

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

abnormal miniature inhibitory postsynaptic currents Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal miniature inhibitory postsynaptic currents phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal osteocyte morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal axillary lymph node morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal costal cartilage morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal splenocyte morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal circulating chemokine level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal circulating chemokine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cerebellum posterior vermis morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal thalamus morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hair medulla air spaces Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hair medulla air spaces phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal zigzag hair morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal xenobiotic induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal xenobiotic induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal kidney epithelium morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal pons morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal b cell anergy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal b cell anergy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal rr interval Gene Set

From MPO Gene-Phenotype Associations

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

abnormal somite size Gene Set

From MPO Gene-Phenotype Associations

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

abnormal pancreatic acinar cell zymogen granule morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal pancreatic acinar cell zymogen granule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal meibomian gland development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal meibomian gland development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal basophil physiology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cerebellum vermis lobule ii morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cerebellum vermis lobule ii morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal tubuloglomerular feedback response Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal tubuloglomerular feedback response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal b wave amplitude Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal b wave amplitude phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal urine organic cation level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal urine organic cation level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal embryo attachment Gene Set

From MPO Gene-Phenotype Associations

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

abnormal myogenesis Gene Set

From MPO Gene-Phenotype Associations

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

abnormal eye morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal kidney collecting duct morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal olfactory bulb granule cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal olfactory bulb granule cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal lumbar dorsal root ganglion morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal lumbar dorsal root ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal sensorimotor gating Gene Set

From MPO Gene-Phenotype Associations

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

abnormal somatic sensory system morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal coccygeal vertebrae morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cell chemotaxis Gene Set

From MPO Gene-Phenotype Associations

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

abnormal neural crest cell apoptosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural crest cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal axon pruning Gene Set

From MPO Gene-Phenotype Associations

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

abnormal pinna reflex Gene Set

From MPO Gene-Phenotype Associations

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

abnormal glomerular capillary morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hind foot hair pigmentation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hind foot hair pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal cord dorsal column morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord dorsal column morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal coronary vessel morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal mucous neck cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal pre-pro b cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal pre-pro b cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal sertoli cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal posterior primitive streak morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal endolymphatic duct morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal pulmonary respiratory rate Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal pulmonary respiratory rate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal gestational length Gene Set

From MPO Gene-Phenotype Associations

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

abnormal thymus medulla morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal long bone epiphysis morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal retinal cone cell inner segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal cone cell inner segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood gas level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood gas level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal suprachiasmatic nucleus morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cortical plate morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hormone-sensitive lipase activity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hormone-sensitive lipase activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal motile cilium morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal male germ cell apoptosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal male germ cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal epididymis size Gene Set

From MPO Gene-Phenotype Associations

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

abnormal catecholamine level Gene Set

From MPO Gene-Phenotype Associations

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

abnormal basal lamina morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal respiration Gene Set

From MPO Gene-Phenotype Associations

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

abnormal vagina development Gene Set

From MPO Gene-Phenotype Associations

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

abnormal skeletal muscle fiber morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal forced expiratory flow rates Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal forced expiratory flow rates phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal right lung morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal lateral nasal prominence morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal sarcolemma morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal vertebral lamina morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal small intestine crypts of lieberkuhn morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal small intestine crypts of lieberkuhn morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal postimplantation uterine environment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal postimplantation uterine environment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal spinal cord white matter morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal spinal cord white matter morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal cone bipolar cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal cone bipolar cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal placenta size Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cajal body morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal olfactory system physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal olfactory system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cd8-positive, gamma-delta intraepithelial t cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cd8-positive, gamma-delta intraepithelial t cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neural crest cell physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal neural crest cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cornea morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal osteoblast physiology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal auchene hair morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal anal canal morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal t-helper 17 cell morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal t-helper 17 cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal uterine horn morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal splenocyte proliferation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal body temperature Gene Set

From MPO Gene-Phenotype Associations

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

abnormal atrium myocardium morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal plasma cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal plasma cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal hyperactivated sperm motility Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal hyperactivated sperm motility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal mammary gland pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal mammary gland pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal endometrium morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal eosinophil differentiation Gene Set

From MPO Gene-Phenotype Associations

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

abnormal circulating estradiol level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal circulating estradiol level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal anxiety-related response Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal anxiety-related response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal conditioned emotional response Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal conditioned emotional response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal neurocranium morphology Gene Set

From MPO Gene-Phenotype Associations

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

abnormal circulating glucagon level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal circulating glucagon level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal functional residual capacity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal functional residual capacity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.