Name

cns hypomyelination Gene Set

From HPO Gene-Disease Associations

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

Hypomyelination and Congenital Cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomyelination and Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypomyelination, global cerebral Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomyelination, global cerebral phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypomyelination, Global Cerebral Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypomyelination, Global Cerebral from the curated CTD Gene-Disease Associations dataset.

hypomyelination Gene Set

From GeneRIF Biological Term Annotations

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

cerebral hypomyelination Gene Set

From HPO Gene-Disease Associations

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

peripheral hypomyelination Gene Set

From HPO Gene-Disease Associations

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

hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, dystonia, and cerebral hypomyelination Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, dystonia, and cerebral hypomyelination phenotype from the curated OMIM Gene-Disease Associations dataset.

hypomyelination, global cerebral Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypomyelination, global cerebral phenotype from the curated OMIM Gene-Disease Associations dataset.

CNS-P53 complex Gene Set

From CORUM Protein Complexes

proteins in the CNS-P53 complex protein complex from the CORUM Protein Complexes dataset.

CNS-5161 Gene Set

From DrugBank Drug Targets

interacting proteins for the CNS-5161 drug from the curated DrugBank Drug Targets dataset.

cns Gene Set

From GeneRIF Biological Term Annotations

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

cns infection Gene Set

From GWASdb SNP-Phenotype Associations

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

cns demyelination Gene Set

From HPO Gene-Disease Associations

genes associated with the cns demyelination 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.

foam cells in visceral organs and cns Gene Set

From HPO Gene-Disease Associations

genes associated with the foam cells in visceral organs and cns phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cns infection Gene Set

From HPO Gene-Disease Associations

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

delayed cns myelination Gene Set

From HPO Gene-Disease Associations

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

Demyelinating Autoimmune Diseases, CNS Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Demyelinating Autoimmune Diseases, CNS phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

decreased cns synapse formation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased cns synapse formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cns synapse formation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cns synapse formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cns synaptic transmission Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cns synaptic transmission phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cns inflammation Gene Set

From MPO Gene-Phenotype Associations

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

increased cns synapse formation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased cns synapse formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cns glial cell morphology Gene Set

From MPO Gene-Phenotype Associations

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

delayed cns synapse formation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the delayed cns synapse formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cns ischemia Gene Set

From MPO Gene-Phenotype Associations

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

altered response to cns ischemic injury Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the altered response to cns ischemic injury phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

cavernous malformations of cns and retina Gene Set

From OMIM Gene-Disease Associations

genes associated with the cavernous malformations of cns and retina phenotype from the curated OMIM Gene-Disease Associations dataset.

cns cell line Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue cns cell line in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.