Cerebellar Degeneration, Subacute

Filters:

Results for "Cerebellar Degeneration, Subacute": 14 genes, 974 gene sets

Name
LOC101060399 Gene cerebellar degeneration-related protein 2
CDR2L Gene cerebellar degeneration-related protein 2-like Enables identical protein binding activity. Predicted to be involved in Golgi to secretory granule transport and vesicle transport along microtubule. Predicted to be located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025]
CDR3 Gene Cerebellar degeneration-related autoantigen-3
CDR2 Gene cerebellar degeneration-related protein 2, 62kDa Predicted to be located in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025]
CDR1 Gene cerebellar degeneration-related protein 1, 34kDa Autoantibodies directed against the protein encoded by this intronless gene have been found in some patients with paraneoplastic cerebellar degeneration. The encoded protein contains several hexapeptide repeats. [provided by RefSeq, Jan 2010]
CLA3 Gene cerebellar ataxia 3 (cerebellar parenchyma disorder 1)
RD3L Gene retinal degeneration 3-like
PRPH2 Gene peripherin 2 (retinal degeneration,* slow)* The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is a cell surface glycoprotein found in the outer segment of both rod and cone photoreceptor cells. It may function as an adhesion molecule involved in stabilization and compaction of outer segment disks or in the maintenance of the curvature of the rim. This protein is essential for disk morphogenesis. Defects in this gene are associated with both central and peripheral retinal degenerations. Some of the various phenotypically different disorders are autosomal dominant retinitis pigmentosa, progressive macular degeneration, macular dystrophy and retinitis pigmentosa digenic. [provided by RefSeq, Jul 2008]
PRCD Gene progressive rod-cone degeneration This gene is predominantly expressed in the retina, and mutations in this gene are the cause of autosomal recessive retinal degeneration in both humans and dogs. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Mar 2010]
RD3 Gene retinal degeneration 3 This gene encodes a retinal protein that is associated with promyelocytic leukemia-gene product (PML) bodies in the nucleus. Mutations in this gene cause Leber congenital amaurosis type 12, a disease that results in retinal degeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]
CLAM Gene cerebellar atrophy with progressive microcephaly
CCCSX Gene Cerebral-cerebellar-coloboma syndrome, X-linked
CHMRQ Gene Cerebellar hypoplasia, mental retardation, and quadrupedal locomotion
ATCAY Gene ataxia, cerebellar, Cayman type This gene encodes a neuron-restricted protein that contains a CRAL-TRIO motif common to proteins that bind small lipophilic molecules. Mutations in this gene are associated with cerebellar ataxia, Cayman type. [provided by RefSeq, Jul 2008]
Cerebellar Degeneration, Subacute Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Degeneration, Subacute in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Subacute Combined Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Subacute Combined Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 3 from the curated CTD Gene-Disease Associations dataset.
primary cerebellar degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease primary cerebellar degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
Cerebellar degeneration-related protein 2 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Cerebellar degeneration-related protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
infantile cerebellar-retinal degeneration Gene Set From OMIM Gene-Disease Associations genes associated with the infantile cerebellar-retinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset.
Cerebellar Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Infantile Cerebellar-Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Infantile Cerebellar-Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cerebellar Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cerebellar Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Paraneoplastic Cerebellar Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Paraneoplastic Cerebellar Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Paraneoplastic Cerebellar Degeneration, Anti-Yo-Associated Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Paraneoplastic Cerebellar Degeneration, Anti-Yo-Associated in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Primary cerebellar degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Primary cerebellar degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile cerebellar-retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Infantile cerebellar-retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Infantile cerebellar-retinal degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile cerebellar-retinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
macular degeneration; nephritis, hereditary; retinal degeneration; retinal drusen Gene Set From GAD Gene-Disease Associations genes associated with the disease macular degeneration; nephritis, hereditary; retinal degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
eye diseases, hereditary; macular degeneration; retinal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease eye diseases, hereditary; macular degeneration; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
Subacute neuronopathic Gaucher's disease Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Subacute neuronopathic Gaucher's disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
subacute glomerulonephritis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease subacute glomerulonephritis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
subacute bacterial endocarditis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease subacute bacterial endocarditis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
subacute lymphocytic thyroiditis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease subacute lymphocytic thyroiditis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
subacute thyroiditis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease subacute thyroiditis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
subacute sclerosing panencephalitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease subacute sclerosing panencephalitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
subacute myeloid leukemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease subacute myeloid leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
subacute g(m2) gangliosidosis Gene Set From GAD Gene-Disease Associations genes associated with the disease subacute g(m2) gangliosidosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
thryoiditis, subacute granulomatous Gene Set From GAD Gene-Disease Associations genes associated with the disease thryoiditis, subacute granulomatous in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dawson's inclusion body encephalitis; subacute sclerosing panencephalitis Gene Set From GAD Gene-Disease Associations genes associated with the disease dawson's inclusion body encephalitis; subacute sclerosing panencephalitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
panencephalitis, subacute sclerosing Gene Set From GAD Gene-Disease Associations genes associated with the disease panencephalitis, subacute sclerosing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
subacute sclerosing panencephalitis Gene Set From GAD Gene-Disease Associations genes associated with the disease subacute sclerosing panencephalitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
subacute Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term subacute in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
subacute progressive viral hepatitis Gene Set From HPO Gene-Disease Associations genes associated with the subacute progressive viral hepatitis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Thyroiditis, Subacute Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Thyroiditis, Subacute phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Subacute Sclerosing Panencephalitis Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Subacute Sclerosing Panencephalitis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Subacute Sclerosing Panencephalitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Subacute Sclerosing Panencephalitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Rasmussen Subacute Encephalitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Rasmussen Subacute Encephalitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Subacute Bacterial Endocarditis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Subacute Bacterial Endocarditis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Necrotizing Encephalopathy, Infantile Subacute, Of Leigh Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Necrotizing Encephalopathy, Infantile Subacute, Of Leigh in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Subacute Thyroiditis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Subacute Thyroiditis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Subacute Cutaneous Lupus Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Subacute Cutaneous Lupus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute And Subacute Liver Necrosis (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute And Subacute Liver Necrosis (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Subacute Dermatitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Subacute Dermatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Subacute Hepatic Necrosis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Subacute Hepatic Necrosis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Subacute Adenoviral Encephalitis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Subacute Adenoviral Encephalitis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lupus Erythematosus, Subacute Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lupus Erythematosus, Subacute in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atypical Subacute Thyroiditis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atypical Subacute Thyroiditis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Subacute Necrotising Encephalomyopathy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Subacute Necrotising Encephalomyopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Subacute Progressive Viral Hepatitis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Subacute Progressive Viral Hepatitis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Subacute sclerosing panencephalitis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Subacute sclerosing panencephalitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Subacute thyroiditis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Subacute thyroiditis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Subacute bacterial endocarditis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Subacute bacterial endocarditis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Subacute lymphocytic thyroiditis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Subacute lymphocytic thyroiditis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Subacute leukemia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Subacute leukemia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Subacute delirium Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Subacute delirium in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Subacute glomerulonephritis Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Subacute glomerulonephritis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
cerebellar hemisphere Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in cerebellar hemisphere relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
dorsolateral (non-cerebellar) part of isA Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in dorsolateral (non-cerebellar) part of isA relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
mantle zone of cerebellar vermis Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in mantle zone of cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
cerebellar white matter Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in cerebellar white matter relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
white matter of cerebellar vermis Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in white matter of cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
lateral (dentate) cerebellar nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in lateral (dentate) cerebellar nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
cerebellar vermis Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
cerebellar nuclei of CbH Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in cerebellar nuclei of CbH relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Cerebellar nuclei Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cerebellar nuclei relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
cortex of cerebellar hemisphere Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in cortex of cerebellar hemisphere relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
intermediate (interpositus) cerebellar nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in intermediate (interpositus) cerebellar nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
cortex of cerebellar vermis Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in cortex of cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
superficial stratum of cerebellar vermis Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in superficial stratum of cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
medial (fastigial) cerebellar nucleus Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in medial (fastigial) cerebellar nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
cerebellar nuclei of CbV Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in cerebellar nuclei of CbV relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
superficial stratum of cerebellar hemisphere Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in superficial stratum of cerebellar hemisphere relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
intermediate stratum of cerebellar vermis Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in intermediate stratum of cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
Cerebellar cortex Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Cerebellar cortex relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
periventricular stratum of cerebellar vermis Gene Set From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in periventricular stratum of cerebellar vermis relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
cerebellar cortex_24 pcw_M_12288 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_3 yrs_F_12836 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_4 mos_M_12296 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_2 yrs_F_12979 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_23 yrs_M_12300 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_21 pcw_F_12365 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_21 pcw_F_12365 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_30 yrs_F_12290 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_13 yrs_F_12831 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_8 yrs_M_12841 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_21 pcw_M_12886 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_3 yrs_M_12980 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_18 yrs_M_12984 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_15 yrs_M_12299 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_4 yrs_M_12298 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_4 yrs_M_12298 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_1 yrs_F_12830 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_21 yrs_F_13057 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_12 pcw_F_13060 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_36 yrs_M_12302 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_17 pcw_F_12880 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_10 mos_M_12977 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_26 pcw_F_12949 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray genes with high or low expression in cerebellar cortex_26 pcw_F_12949 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
cerebellar cortex_24 pcw_M_12288 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_11 yrs_F_12289 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_11 yrs_F_12289 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_40 yrs_F_12304 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_3 yrs_F_12836 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_3 yrs_F_12836 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_4 mos_M_12296 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_23 yrs_M_12300 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_21 pcw_F_12365 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_21 pcw_F_12365 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_30 yrs_F_12290 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_13 yrs_F_12831 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_2 yrs_F_12979 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_37 yrs_M_12303 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_8 yrs_M_12841 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_17 pcw_F_12880 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_21 pcw_M_12886 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_3 yrs_M_12980 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_18 yrs_M_12984 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_15 yrs_M_12299 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_4 yrs_M_12298 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_4 yrs_M_12298 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_8 yrs_M_12981 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_8 yrs_M_12981 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_4 mos_M_12890 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_4 mos_M_12890 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_1 yrs_F_12830 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_16 pcw_M_12837 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_19 yrs_F_12832 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_19 yrs_F_12832 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_21 yrs_F_13057 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_12 pcw_F_13060 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_37 pcw_M_263195015 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_37 pcw_M_263195015 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_36 yrs_M_12302 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_10 mos_M_12977 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar cortex_35 pcw_F_12295 Gene Set From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq genes with high or low expression in cerebellar cortex_35 pcw_F_12295 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
cerebellar vermis Gene Set From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in cerebellar vermis relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
Cognitive impairment with or without cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cognitive impairment with or without cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia infantile with progressive external ophthalmoplegia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia infantile with progressive external ophthalmoplegia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia and hypogonadotropic hypogonadism Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia and hypogonadotropic hypogonadism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, deafness, and narcolepsy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, deafness, and narcolepsy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Diabetes mellitus, permanent neonatal, with cerebellar agenesis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Diabetes mellitus, permanent neonatal, with cerebellar agenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Aniridia, cerebellar ataxia, and mental retardation Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Aniridia, cerebellar ataxia, and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
cerebellar mossy fiber Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the cerebellar mossy fiber cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
cerebellar mossy fiber Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cerebellar mossy fiber cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
Aniridia cerebellar ataxia mental deficiency Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Aniridia cerebellar ataxia mental deficiency from the curated CTD Gene-Disease Associations dataset.
Diabetes Mellitus, Permanent Neonatal, with Cerebellar Agenesis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Diabetes Mellitus, Permanent Neonatal, with Cerebellar Agenesis from the curated CTD Gene-Disease Associations dataset.
Cerebellar Ataxia, Cayman Type Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebellar Ataxia, Cayman Type from the curated CTD Gene-Disease Associations dataset.
Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 from the curated CTD Gene-Disease Associations dataset.
Cerebellar Diseases Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebellar Diseases from the curated CTD Gene-Disease Associations dataset.
Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset.
Cerebellar Ataxia Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebellar Ataxia from the curated CTD Gene-Disease Associations dataset.
Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 from the curated CTD Gene-Disease Associations dataset.
Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance from the curated CTD Gene-Disease Associations dataset.
cerebellar disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cerebellar disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
cerebellar disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebellar disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebellar liponeurocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebellar liponeurocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebellar ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebellar ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebellar medulloblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebellar medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebellar astrocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebellar astrocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebellar angioblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebellar angioblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
myoclonic cerebellar dyssynergia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease myoclonic cerebellar dyssynergia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
huntington disease; myoclonic cerebellar dyssynergia; spinocerebellar ataxias Gene Set From GAD Gene-Disease Associations genes associated with the disease huntington disease; myoclonic cerebellar dyssynergia; spinocerebellar ataxias in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain neoplasms; cerebellar neoplasms; ganglioglioma; glioma; medulloblastoma; neuroectodermal tumor, primitive; neuroectodermal tumors, primitive Gene Set From GAD Gene-Disease Associations genes associated with the disease brain neoplasms; cerebellar neoplasms; ganglioglioma; glioma; medulloblastoma; neuroectodermal tumor, primitive; neuroectodermal tumors, primitive in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebellar ataxia; Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebellar ataxia; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebellar medulloblastomas and cutaneous basal cell carcinomas. Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebellar medulloblastomas and cutaneous basal cell carcinomas. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebellar neoplasms; medulloblastoma Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebellar neoplasms; medulloblastoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebellar neoplasms; hemangioblastoma; von hippel-lindau disease Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebellar neoplasms; hemangioblastoma; von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebellar volume Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebellar volume in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebellar ataxia Gene Set From GAD Gene-Disease Associations genes associated with the disease cerebellar ataxia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adrenal gland neoplasms; carcinoma, renal cell; cerebellar neoplasms; hemangioblastoma; kidney neoplasms; pheochromocytoma; retinal neoplasms; von hippel-lindau disease Gene Set From GAD Gene-Disease Associations genes associated with the disease adrenal gland neoplasms; carcinoma, renal cell; cerebellar neoplasms; hemangioblastoma; kidney neoplasms; pheochromocytoma; retinal neoplasms; von hippel-lindau disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cerebellar Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term cerebellar in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
CSTB_KO_GSE47516_18_mouse_brain (P7 cerebellum, P30 cerebellum, cerebellar granule cells) Gene Set From GEO Signatures of Differentially Expressed Genes for Gene Perturbations genes differentially expressed following the CSTB_KO_GSE47516_18_mouse_brain (P7 cerebellum, P30 cerebellum, cerebellar granule cells) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.
regulation of cerebellar granule cell precursor proliferation Gene Set From GO Biological Process Annotations 2015 genes participating in the regulation of cerebellar granule cell precursor proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar cortex structural organization Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar cortex structural organization biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar granular layer development Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar granular layer development biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar purkinje cell layer morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar purkinje cell layer morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar purkinje cell differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar purkinje cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar cortex formation Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar cortex formation biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar cortex morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar cortex morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar granule cell precursor tangential migration Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar granule cell precursor tangential migration biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar molecular layer development Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar molecular layer development biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar purkinje cell layer structural organization Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar purkinje cell layer structural organization biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar purkinje cell layer development Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar purkinje cell layer development biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar cortex development Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar cortex development biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar purkinje cell-granule cell precursor cell signaling involved in regulation of granule cell precursor cell proliferation Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar purkinje cell-granule cell precursor cell signaling involved in regulation of granule cell precursor cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
negative regulation of cerebellar granule cell precursor proliferation Gene Set From GO Biological Process Annotations 2015 genes participating in the negative regulation of cerebellar granule cell precursor proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar granule cell precursor proliferation Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar granule cell precursor proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
radial glia guided migration of cerebellar granule cell Gene Set From GO Biological Process Annotations 2015 genes participating in the radial glia guided migration of cerebellar granule cell biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar granular layer morphogenesis Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar granular layer morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset.
smoothened signaling pathway involved in regulation of cerebellar granule cell precursor cell proliferation Gene Set From GO Biological Process Annotations 2015 genes participating in the smoothened signaling pathway involved in regulation of cerebellar granule cell precursor cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
positive regulation of cerebellar granule cell precursor proliferation Gene Set From GO Biological Process Annotations 2015 genes participating in the positive regulation of cerebellar granule cell precursor proliferation biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar purkinje cell layer maturation Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar purkinje cell layer maturation biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar granule cell differentiation Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar granule cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar granular layer structural organization Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar granular layer structural organization biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar granular layer maturation Gene Set From GO Biological Process Annotations 2015 genes participating in the cerebellar granular layer maturation biological process from the curated GO Biological Process Annotations 2015 dataset.
cerebellar mossy fiber Gene Set From GO Cellular Component Annotations 2015 proteins localized to the cerebellar mossy fiber cellular component from the curated GO Cellular Component Annotations 2015 dataset.
abnormality of the cerebellar peduncle Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the cerebellar peduncle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia of the inferior half of the cerebellar vermis Gene Set From HPO Gene-Disease Associations genes associated with the aplasia of the inferior half of the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar cortical atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar cortical atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
thickened superior cerebellar peduncle Gene Set From HPO Gene-Disease Associations genes associated with the thickened superior cerebellar peduncle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
agenesis of cerebellar vermis Gene Set From HPO Gene-Disease Associations genes associated with the agenesis of cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
diffuse cerebellar atrophy Gene Set From HPO Gene-Disease Associations genes associated with the diffuse cerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar cyst Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar cyst phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
nonprogressive cerebellar ataxia Gene Set From HPO Gene-Disease Associations genes associated with the nonprogressive cerebellar ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
aplasia/hypoplasia of the cerebellar vermis Gene Set From HPO Gene-Disease Associations genes associated with the aplasia/hypoplasia of the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
elongated superior cerebellar peduncle Gene Set From HPO Gene-Disease Associations genes associated with the elongated superior cerebellar peduncle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
dysgenesis of the cerebellar vermis Gene Set From HPO Gene-Disease Associations genes associated with the dysgenesis of the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar vermis atrophy Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar vermis atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar hemisphere hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar hemisphere hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar hemorrhage Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar hemorrhage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar vermis hypoplasia Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar vermis hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar dysplasia Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
disorganization of the anterior cerebellar vermis Gene Set From HPO Gene-Disease Associations genes associated with the disorganization of the anterior cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the superior cerebellar peduncle Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the superior cerebellar peduncle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
abnormality of the cerebellar vermis Gene Set From HPO Gene-Disease Associations genes associated with the abnormality of the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar malformation Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar malformation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar calcifications Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar calcifications phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebellar hemangioblastoma Gene Set From HPO Gene-Disease Associations genes associated with the cerebellar hemangioblastoma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
loss of purkinje cells in the cerebellar vermis Gene Set From HPO Gene-Disease Associations genes associated with the loss of purkinje cells in the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive cerebellar ataxia Gene Set From HPO Gene-Disease Associations genes associated with the progressive cerebellar ataxia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
dense calcifications in the cerebellar dentate nucleus Gene Set From HPO Gene-Disease Associations genes associated with the dense calcifications in the cerebellar dentate nucleus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Cerebellar Diseases Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cerebellar Diseases phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cerebellar Ataxia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cerebellar Ataxia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Cerebellar Neoplasms Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Cerebellar Neoplasms phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Myoclonic Cerebellar Dyssynergia Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Myoclonic Cerebellar Dyssynergia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
thin cerebellar molecular layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thin cerebellar molecular layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar molecular layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar molecular layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar lobule formation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar lobule formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar hemisphere morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar hemisphere morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar purkinje cell layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar purkinje cell layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
decreased cerebellar granule cell number Gene Set From MPO Gene-Phenotype Associations gene mutations causing the decreased cerebellar granule cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent cerebellar foliation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent cerebellar foliation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent cerebellar granule cells Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent cerebellar granule cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar layer morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
thin cerebellar granule layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the thin cerebellar granule layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar granule layer morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar granule layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar golgi cell morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar golgi cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar peduncle morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar peduncle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
reduced cerebellar foliation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the reduced cerebellar foliation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent cerebellar lobules Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent cerebellar lobules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar granule cell morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar granule cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar cortex morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar cortex morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
delaminated cerebellar granule layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the delaminated cerebellar granule layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ectopic cerebellar granule cells Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ectopic cerebellar granule cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar plate morphology Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar plate morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar granule cell migration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar granule cell migration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar foliation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar foliation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
absent cerebellar granule layer Gene Set From MPO Gene-Phenotype Associations gene mutations causing the absent cerebellar granule layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal cerebellar granule cell proliferation Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar granule cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1 phenotype from the curated OMIM Gene-Disease Associations dataset.
cognitive impairment with or without cerebellar ataxia Gene Set From OMIM Gene-Disease Associations genes associated with the cognitive impairment with or without cerebellar ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance phenotype from the curated OMIM Gene-Disease Associations dataset.
?cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene Set From OMIM Gene-Disease Associations genes associated with the ?cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.
ataxia, cerebellar, cayman type Gene Set From OMIM Gene-Disease Associations genes associated with the ataxia, cerebellar, cayman type phenotype from the curated OMIM Gene-Disease Associations dataset.
migraine, familial hemiplegic, 1, with progressive cerebellar ataxia Gene Set From OMIM Gene-Disease Associations genes associated with the migraine, familial hemiplegic, 1, with progressive cerebellar ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.
mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebellar ataxia, nonprogressive, with mental retardation Gene Set From OMIM Gene-Disease Associations genes associated with the cerebellar ataxia, nonprogressive, with mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebellar ataxia Gene Set From OMIM Gene-Disease Associations genes associated with the cerebellar ataxia phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3 Gene Set From OMIM Gene-Disease Associations genes associated with the cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
hemangioblastoma, cerebellar, somatic Gene Set From OMIM Gene-Disease Associations genes associated with the hemangioblastoma, cerebellar, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebral-cerebellar-coloboma syndrome, x-linked Gene Set From OMIM Gene-Disease Associations genes associated with the cerebral-cerebellar-coloboma syndrome, x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.
pancreatic and cerebellar agenesis Gene Set From OMIM Gene-Disease Associations genes associated with the pancreatic and cerebellar agenesis phenotype from the curated OMIM Gene-Disease Associations dataset.
microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set From OMIM Gene-Disease Associations genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebellar ataxia and hypogonadotropic hypogonadism Gene Set From OMIM Gene-Disease Associations genes associated with the cerebellar ataxia and hypogonadotropic hypogonadism phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebellar ataxia, deafness, and narcolepsy, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the cerebellar ataxia, deafness, and narcolepsy, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
cerebellar Gene Set From Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term cerebellar in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.
cerebellar granule cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cerebellar granule cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
cerebellar nucleus Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cerebellar nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
cerebellar cortex Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cerebellar cortex in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
cerebellar purkinje cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue cerebellar purkinje cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.
Cerebellar Malformation Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Malformation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Hypoplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Congenital Cerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Congenital Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Hemangioblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Hemangioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Dominant Cerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Dominant Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Progressive Cerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Progressive Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Function Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Function in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Medulloblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Medulloblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessie Cerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessie Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Lesion Nos Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Lesion Nos in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Liponeurocytoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Liponeurocytoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Glioblastoma Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Glioblastoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Ischaemia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Ischaemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Marie Cerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Marie Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Multiple System Atrophy, Cerebellar Variant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Multiple System Atrophy, Cerebellar Variant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Cortical Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Cortical Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Cortical Dysplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Cortical Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Decompression Injury Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Decompression Injury in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Thickened Superior Cerebellar Peduncle Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Thickened Superior Cerebellar Peduncle in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Edema Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Edema in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Dysgenesis Of The Cerebellar Vermis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Dysgenesis Of The Cerebellar Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Stroke Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Stroke in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Granule Cell Hypertrophy And Megalencephaly Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Granule Cell Hypertrophy And Megalencephaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Cognitive Affective Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Cognitive Affective Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Infarction Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Infarction in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myoclonic Cerebellar Dyssynergia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myoclonic Cerebellar Dyssynergia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mega-Corpus-Callosum Syndrome With Cerebellar Hypoplasia And Cortical Malformations Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mega-Corpus-Callosum Syndrome With Cerebellar Hypoplasia And Cortical Malformations in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Abnormality Of The Cerebellar Vermis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of The Cerebellar Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Partial Absence Of Cerebellar Vermis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Partial Absence Of Cerebellar Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late Cortical Cerebellar Atrophy Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late Cortical Cerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Polymicrogyria, Perisylvian, With Cerebellar Hypoplasia And Arthrogryposis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Polymicrogyria, Perisylvian, With Cerebellar Hypoplasia And Arthrogryposis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Cerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Agenesis Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Agenesis in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cognitive Impairment With Or Without Cerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cognitive Impairment With Or Without Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Degenerations, Primary Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Degenerations, Primary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Hemisphere Hypoplasia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cerebellar Hemisphere Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spectrin-Associated Autosomal Recessive Cerebellar Ataxia Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spectrin-Associated Autosomal Recessive Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Autosomal Recessive Cerebellar Ataxia Type 1 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Autosomal Recessive Cerebellar Ataxia Type 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Acute Cerebellar Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Acute Cerebellar Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
X-Linked Cerebral, Cerebellar, Coloboma Syndrome Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease X-Linked Cerebral, Cerebellar, Coloboma Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Childhood Cerebellar Neoplasm Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Childhood Cerebellar Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cerebellar Ataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Signs Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Signs in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Dysmetria Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Dysmetria in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Nonprogressive Cerebellar Ataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nonprogressive Cerebellar Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Hemorrhage Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Hemorrhage in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Vermis Hypoplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Vermis Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia/Hypoplasia Of The Cerebellar Vermis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia/Hypoplasia Of The Cerebellar Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Elongated Superior Cerebellar Peduncle Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Elongated Superior Cerebellar Peduncle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Loss Of Purkinje Cells In The Cerebellar Vermis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Purkinje Cells In The Cerebellar Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Purkinje Layer Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Purkinje Layer Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Gait Ataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Gait Ataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Vermis Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Vermis Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Cyst Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Cyst in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Dysplasia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Diffuse Cerebellar Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Diffuse Cerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Calcifications Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Calcifications in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Fusion Of The Cerebellar Hemispheres Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fusion Of The Cerebellar Hemispheres in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of The Superior Cerebellar Peduncle Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Superior Cerebellar Peduncle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Atrophy Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Atrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Disorganization Of The Anterior Cerebellar Vermis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Disorganization Of The Anterior Cerebellar Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Dense Calcifications In The Cerebellar Dentate Nucleus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dense Calcifications In The Cerebellar Dentate Nucleus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Gliosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Gliosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormal Morphology Of The Cerebellar Cortex Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Morphology Of The Cerebellar Cortex in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Hypoplasia With Endosteal Sclerosis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Hypoplasia With Endosteal Sclerosis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cerebellar Hemiataxia Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cerebellar Hemiataxia in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Abnormality Of The Cerebellar Peduncle Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of The Cerebellar Peduncle in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Small Cerebellar Cortex Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Small Cerebellar Cortex in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Aplasia Of The Inferior Half Of The Cerebellar Vermis Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Aplasia Of The Inferior Half Of The Cerebellar Vermis in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
cerebellar granule cell differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the cerebellar granule cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
cerebellar granule cell precursor proliferation Gene Set From GO Biological Process Annotations 2023 genes participating in the cerebellar granule cell precursor proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
cerebellar Purkinje cell differentiation Gene Set From GO Biological Process Annotations 2023 genes participating in the cerebellar Purkinje cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset.
cerebellar Purkinje cell-granule cell precursor cell signaling involved in regulation of granule cell precursor cell proliferation Gene Set From GO Biological Process Annotations 2023 genes participating in the cerebellar Purkinje cell-granule cell precursor cell signaling involved in regulation of granule cell precursor cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
cerebellar granule cell precursor tangential migration Gene Set From GO Biological Process Annotations 2023 genes participating in the cerebellar granule cell precursor tangential migration biological process from the curated GO Biological Process Annotations 2023 dataset.
cerebellar granular layer maturation Gene Set From GO Biological Process Annotations 2023 genes participating in the cerebellar granular layer maturation biological process from the curated GO Biological Process Annotations 2023 dataset.
radial glia guided migration of cerebellar granule cell Gene Set From GO Biological Process Annotations 2023 genes participating in the radial glia guided migration of cerebellar granule cell biological process from the curated GO Biological Process Annotations 2023 dataset.
positive regulation of cerebellar granule cell precursor proliferation Gene Set From GO Biological Process Annotations 2023 genes participating in the positive regulation of cerebellar granule cell precursor proliferation biological process from the curated GO Biological Process Annotations 2023 dataset.
cerebellar cortex maturation Gene Set From GO Biological Process Annotations 2023 genes participating in the cerebellar cortex maturation biological process from the curated GO Biological Process Annotations 2023 dataset.
cerebellar mossy fiber Gene Set From GO Cellular Component Annotations 2023 proteins localized to the cerebellar mossy fiber cellular component from the curated GO Cellular Component Annotations 2023 dataset.
abnormal cerebellar granule cell morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar granule cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar plate morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar plate morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar molecular layer Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar molecular layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
thin cerebellar molecular layer Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the thin cerebellar molecular layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar foliation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar foliation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar granule layer morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar granule layer morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased cerebellar granule cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cerebellar granule cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar layer morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar layer morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar Purkinje cell layer Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar Purkinje cell layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
thin cerebellar granule layer Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the thin cerebellar granule layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent cerebellar granule cells Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent cerebellar granule cells phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
delaminated cerebellar granule layer Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the delaminated cerebellar granule layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased cerebellar foliation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cerebellar foliation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar cortex morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar cortex morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent cerebellar foliation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent cerebellar foliation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar lobule formation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar lobule formation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent cerebellar lobules Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent cerebellar lobules phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
reduced cerebellar foliation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced cerebellar foliation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
ectopic cerebellar granule cells Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ectopic cerebellar granule cells phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar granule cell migration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar granule cell migration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar Golgi cell morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar Golgi cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
absent cerebellar granule layer Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the absent cerebellar granule layer phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
decreased cerebellar granule cell precursor proliferation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cerebellar granule cell precursor proliferation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar glomerulus morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar glomerulus morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar peduncle morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar peduncle morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar granule cell precursor proliferation Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar granule cell precursor proliferation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal cerebellar hemisphere morphology Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cerebellar hemisphere morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
increased cerebellar granule cell number Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cerebellar granule cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Brain - Cerebellar Hemisphere Gene Set From GTEx Tissue Gene Expression Profiles 2023 genes with high or low expression in Brain - Cerebellar Hemisphere relative to other tissues from the GTEx Tissue Gene Expression Profiles 2023 dataset.
Cerebellar interneuron_Brain_Mouse Gene Set From CellMarker Gene-Cell Type Associations genes associated with the Cerebellar interneuron_Brain_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset.
cerebellar granule cell differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the cerebellar granule cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
cerebellar granule cell precursor proliferation Gene Set From GO Biological Process Annotations 2025 genes participating in the cerebellar granule cell precursor proliferation biological process from the curated GO Biological Process Annotations 2025 dataset.
cerebellar Purkinje cell differentiation Gene Set From GO Biological Process Annotations 2025 genes participating in the cerebellar Purkinje cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset.
cerebellar Purkinje cell-granule cell precursor cell signaling Gene Set From GO Biological Process Annotations 2025 genes participating in the cerebellar Purkinje cell-granule cell precursor cell signaling biological process from the curated GO Biological Process Annotations 2025 dataset.
cerebellar granule cell precursor tangential migration Gene Set From GO Biological Process Annotations 2025 genes participating in the cerebellar granule cell precursor tangential migration biological process from the curated GO Biological Process Annotations 2025 dataset.
cerebellar granular layer maturation Gene Set From GO Biological Process Annotations 2025 genes participating in the cerebellar granular layer maturation biological process from the curated GO Biological Process Annotations 2025 dataset.
radial glia guided migration of cerebellar granule cell Gene Set From GO Biological Process Annotations 2025 genes participating in the radial glia guided migration of cerebellar granule cell biological process from the curated GO Biological Process Annotations 2025 dataset.
cerebellar cortex maturation Gene Set From GO Biological Process Annotations 2025 genes participating in the cerebellar cortex maturation biological process from the curated GO Biological Process Annotations 2025 dataset.
cerebellar mossy fiber Gene Set From GO Cellular Component Annotations 2025 proteins localized to the cerebellar mossy fiber cellular component from the curated GO Cellular Component Annotations 2025 dataset.
Cerebellar disease Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cerebellar disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal dominant cerebellar ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal dominant cerebellar ataxia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cerebellar ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cerebellar ataxia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Autosomal recessive cerebellar ataxia Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Autosomal recessive cerebellar ataxia from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cerebellar medulloblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant cerebellar ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant cerebellar ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar disease Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar astrocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar astrocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal recessive cerebellar ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive cerebellar ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar hypoplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar hypoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar ataxia type 48 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar ataxia type 48 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar ataxia type 41 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar ataxia type 41 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar ataxia type 42 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar ataxia type 42 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Myoclonic cerebellar dyssynergia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Myoclonic cerebellar dyssynergia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia and hydranencephaly in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Nonprogressive cerebellar ataxia with mental retardation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Nonprogressive cerebellar ataxia with mental retardation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar ataxia, mental retardation and dysequlibrium syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar ataxia, mental retardation and dysequlibrium syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Autosomal dominant cerebellar ataxia, deafness and narcolepsy Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant cerebellar ataxia, deafness and narcolepsy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cayman type cerebellar ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cayman type cerebellar ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar liponeurocytoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar liponeurocytoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar vermis medulloblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar vermis medulloblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar ataxia type 47 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar ataxia type 47 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar atrophy, visual impairment, and psychomotor retardation Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar atrophy, visual impairment, and psychomotor retardation in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar ataxia type 43 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar ataxia type 43 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked cerebellar ataxia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked cerebellar ataxia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar ataxia type 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar ataxia type 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Neurodevelopmental disorder with cerebellar atrophy and motor dysfunction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Lissencephaly 7 with cerebellar hypoplasia Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lissencephaly 7 with cerebellar hypoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar angioblastoma Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebellar angioblastoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebellar cortex Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cerebellar cortex in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebellar Purkinje cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cerebellar Purkinje cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebellar granule cell Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cerebellar granule cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebellar nucleus Gene Set From TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cerebellar nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset.
Cerebellar mossy fiber Gene Set From COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Cerebellar mossy fiber cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
Cerebellar granule cell to Purkinje cell synapse Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cerebellar granule cell to Purkinje cell synapse cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Cerebellar climbing fiber to Purkinje cell synapse Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cerebellar climbing fiber to Purkinje cell synapse cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Cerebellar mossy fiber Gene Set From COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cerebellar mossy fiber cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
Congenital cerebellar hypoplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Congenital cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Abortive cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Abortive cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Infantile cerebral and cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Infantile cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal dominant cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked progressive cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked progressive cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Non-progressive congenital cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Non-progressive congenital cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked intellectual disability-cerebellar hypoplasia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked intellectual disability-cerebellar hypoplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar dysfunction Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar dysfunction phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar atrophy Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar-facial-dental syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar-facial-dental syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar hemangioblastoma Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar hemangioblastoma phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar vermis hypoplasia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar vermis hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
X-linked cerebral-cerebellar-coloboma syndrome syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the X-linked cerebral-cerebellar-coloboma syndrome syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Progressive cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Progressive cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Short stature-pituitary and cerebellar defects-small sella turcica syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Short stature-pituitary and cerebellar defects-small sella turcica syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
ITPR1-associated cerebellar ataxia spectrum disorder Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the ITPR1-associated cerebellar ataxia spectrum disorder phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Autosomal recessive cerebellar ataxia-saccadic intrusion syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal recessive cerebellar ataxia-saccadic intrusion syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar ataxia-hypogonadism syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar ataxia-hypogonadism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Hereditary cerebellar ataxia Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Hereditary cerebellar ataxia phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Dysgenesis of the cerebellar vermis Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Dysgenesis of the cerebellar vermis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Abnormal cerebellar vermis morphology Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormal cerebellar vermis morphology phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Macular degeneration, early-onset Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Macular degeneration, early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Retinal degeneration, autosomal recessive, clumped pigment type Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Retinal degeneration, autosomal recessive, clumped pigment type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Juvenile macular degeneration and hypotrichosis Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Juvenile macular degeneration and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Age-related macular degeneration 6 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Age-related macular degeneration 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Age-related macular degeneration 3 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Age-related macular degeneration 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Age-related macular degeneration 11 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Age-related macular degeneration 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Age-related macular degeneration 14 Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Age-related macular degeneration 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Pigmentary pallidal degeneration Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Pigmentary pallidal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Myopia, high, with cataract and vitreoretinal degeneration Gene Set From ClinVar Gene-Phenotype Associations genes associated with the Myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.
Macular Degeneration, Age-Related, 11 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 11 from the curated CTD Gene-Disease Associations dataset.
Macular Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration from the curated CTD Gene-Disease Associations dataset.
Macular Degeneration, Age-Related, 10 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 10 from the curated CTD Gene-Disease Associations dataset.
Snowflake vitreoretinal degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Snowflake vitreoretinal degeneration from the curated CTD Gene-Disease Associations dataset.
Macular Degeneration, Age-Related, 9 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 9 from the curated CTD Gene-Disease Associations dataset.
Macular Degeneration, Age-Related, 3 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 3 from the curated CTD Gene-Disease Associations dataset.
Macular Degeneration, Age-Related, 2 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 2 from the curated CTD Gene-Disease Associations dataset.
Macular Degeneration, Age-Related, 1 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 1 from the curated CTD Gene-Disease Associations dataset.
Macular Degeneration, Age-Related, 7 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 7 from the curated CTD Gene-Disease Associations dataset.
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED from the curated CTD Gene-Disease Associations dataset.
Intervertebral Disc Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Intervertebral Disc Degeneration from the curated CTD Gene-Disease Associations dataset.
Retinal Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Retinal Degeneration from the curated CTD Gene-Disease Associations dataset.
Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration from the curated CTD Gene-Disease Associations dataset.
Nerve Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Nerve Degeneration from the curated CTD Gene-Disease Associations dataset.
Macular Degeneration, Age-Related, 4 Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Macular Degeneration, Age-Related, 4 from the curated CTD Gene-Disease Associations dataset.
Striatonigral degeneration infantile Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Striatonigral degeneration infantile from the curated CTD Gene-Disease Associations dataset.
Striatal Degeneration, Autosomal Dominant Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Striatal Degeneration, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset.
Hyaloideoretinal degeneration of Wagner Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hyaloideoretinal degeneration of Wagner from the curated CTD Gene-Disease Associations dataset.
Juvenile macular degeneration and hypotrichosis Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Juvenile macular degeneration and hypotrichosis from the curated CTD Gene-Disease Associations dataset.
Wallerian Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Wallerian Degeneration from the curated CTD Gene-Disease Associations dataset.
Frontotemporal Lobar Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Frontotemporal Lobar Degeneration from the curated CTD Gene-Disease Associations dataset.
Mental Retardation, Severe, With Spasticity And Pigmentary Tapetoretinal Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Mental Retardation, Severe, With Spasticity And Pigmentary Tapetoretinal Degeneration from the curated CTD Gene-Disease Associations dataset.
Hepatolenticular Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Hepatolenticular Degeneration from the curated CTD Gene-Disease Associations dataset.
Late-Onset Retinal Degeneration Gene Set From CTD Gene-Disease Associations genes/proteins associated with the disease Late-Onset Retinal Degeneration from the curated CTD Gene-Disease Associations dataset.
Macular Degeneration Gene Set From dbGAP Gene-Trait Associations genes associated with the trait Macular Degeneration in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.
macular degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease macular degeneration from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
spinocerebellar degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease spinocerebellar degeneration from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
cerebral degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease cerebral degeneration from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
age related macular degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease age related macular degeneration from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
retinal degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease retinal degeneration from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
degeneration of macula and posterior pole Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease degeneration of macula and posterior pole from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
macular degeneration Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease macular degeneration in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
retinal degeneration Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease retinal degeneration in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.
macular degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease macular degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
striatonigral degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease striatonigral degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
peripheral retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease peripheral retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
spinocerebellar degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease spinocerebellar degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
kuhnt-junius degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease kuhnt-junius degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
corneal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease corneal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cerebral degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cerebral degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
age related macular degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease age related macular degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
conjunctival degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease conjunctival degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
degeneration of macula and posterior pole Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease degeneration of macula and posterior pole in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
cardiovascular diseases; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroidal neovascularization; geographic atrophy; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; geographic atrophy; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease multisystem atrophy, progressive supranuclear palsy and corticobasal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroiditis; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease choroiditis; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blind vision; blindness; retinal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease blind vision; blindness; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
amyotrophic lateral sclerosis; iron metabolism disorders; nerve degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease amyotrophic lateral sclerosis; iron metabolism disorders; nerve degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chlamydia infections; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease chlamydia infections; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular degeneration; stargardt disease Gene Set From GAD Gene-Disease Associations genes associated with the disease macular degeneration; stargardt disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hepatolenticular degeneration; movement disorders Gene Set From GAD Gene-Disease Associations genes associated with the disease hepatolenticular degeneration; movement disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
geographic atrophy; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease geographic atrophy; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroidal neovascularization; macular degeneration; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; macular degeneration; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; nerve degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; alzheimer's disease; aphasia, primary progressive; dementia; nerve degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
age-related macular degeneration (wet) Gene Set From GAD Gene-Disease Associations genes associated with the disease age-related macular degeneration (wet) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis Gene Set From GAD Gene-Disease Associations genes associated with the disease adolescent nephronophthisis, tapeto-retinal degeneration and hepatic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
wet macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease wet macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
autosomal dominant macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease autosomal dominant macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blind vision; blindness; choroidal neovascularization; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease blind vision; blindness; choroidal neovascularization; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cone degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease cone degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
geographic atrophy; macular degeneration; retinal drusen Gene Set From GAD Gene-Disease Associations genes associated with the disease geographic atrophy; macular degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
mitochondrial diseases; nerve degeneration; presbycusis Gene Set From GAD Gene-Disease Associations genes associated with the disease mitochondrial diseases; nerve degeneration; presbycusis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
intervertebral disk degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease intervertebral disk degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular degeneration, age-related Gene Set From GAD Gene-Disease Associations genes associated with the disease macular degeneration, age-related in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
familial age-related macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease familial age-related macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
blindness; retinal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease blindness; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hepatolenticular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease hepatolenticular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroid diseases; macular degeneration; peripheral vascular diseases; retinal neovascularization Gene Set From GAD Gene-Disease Associations genes associated with the disease choroid diseases; macular degeneration; peripheral vascular diseases; retinal neovascularization in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
brain injuries; nerve degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease brain injuries; nerve degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroidal neovascularization; macular degeneration; retinal drusen Gene Set From GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; macular degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular degeneration; neovascularization, pathologic Gene Set From GAD Gene-Disease Associations genes associated with the disease macular degeneration; neovascularization, pathologic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
intervertebral disk degeneration; intervertebral disk displacement Gene Set From GAD Gene-Disease Associations genes associated with the disease intervertebral disk degeneration; intervertebral disk displacement in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
retinal degeneration; retinitis pigmentosa Gene Set From GAD Gene-Disease Associations genes associated with the disease retinal degeneration; retinitis pigmentosa in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
angiomatosis; choroidal neovascularization; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease angiomatosis; choroidal neovascularization; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular degeneration; vision, low Gene Set From GAD Gene-Disease Associations genes associated with the disease macular degeneration; vision, low in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular degeneration; soft drusen Gene Set From GAD Gene-Disease Associations genes associated with the disease macular degeneration; soft drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; hypertension; macular degeneration; prostatic neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; hypertension; macular degeneration; prostatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atherosclerosis; inflammation; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease atherosclerosis; inflammation; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
hepatolenticular degeneration; liver failure, acute Gene Set From GAD Gene-Disease Associations genes associated with the disease hepatolenticular degeneration; liver failure, acute in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disc degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease disc degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroid diseases; macular degeneration; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease choroid diseases; macular degeneration; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
myocardial infarct; cholesterol, hdl; triglycerides; atherosclerosis, coronary; macular degeneration; colorectal cancer Gene Set From GAD Gene-Disease Associations genes associated with the disease myocardial infarct; cholesterol, hdl; triglycerides; atherosclerosis, coronary; macular degeneration; colorectal cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
atrophy; choroidal neovascularization; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease atrophy; choroidal neovascularization; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cataract; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease cataract; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
dna damage; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease dna damage; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroidal neovascularization; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
color vision defects; retinal degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease color vision defects; retinal degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
occupational exposure in lumbar disc degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease occupational exposure in lumbar disc degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nerve degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease nerve degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
disc degeneration, lumbar spine Gene Set From GAD Gene-Disease Associations genes associated with the disease disc degeneration, lumbar spine in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
age-related macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease age-related macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
spinal disc degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease spinal disc degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroid diseases; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease choroid diseases; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
cardiovascular diseases; inflammation; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease cardiovascular diseases; inflammation; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
macular degeneration; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease macular degeneration; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
nerve degeneration; neurodegenerative diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease nerve degeneration; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
degeneration of intervertebral discs Gene Set From GAD Gene-Disease Associations genes associated with the disease degeneration of intervertebral discs in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diseases in twins; macular degeneration; retinal drusen Gene Set From GAD Gene-Disease Associations genes associated with the disease diseases in twins; macular degeneration; retinal drusen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
chlamydophila infections; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease chlamydophila infections; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
ache, low back; intervertebral disk degeneration; low back pain Gene Set From GAD Gene-Disease Associations genes associated with the disease ache, low back; intervertebral disk degeneration; low back pain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
diabetes mellitus, type 2; inflammatory bowel diseases; macular degeneration; prostatic neoplasms Gene Set From GAD Gene-Disease Associations genes associated with the disease diabetes mellitus, type 2; inflammatory bowel diseases; macular degeneration; prostatic neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
alzheimer disease; cardiovascular diseases; colorectal neoplasms; macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease alzheimer disease; cardiovascular diseases; colorectal neoplasms; macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroidal neovascularization; retinal drusen; wet macular degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease choroidal neovascularization; retinal drusen; wet macular degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
choroid diseases; choroidal neovascularization; macular degeneration; peripheral vascular diseases Gene Set From GAD Gene-Disease Associations genes associated with the disease choroid diseases; choroidal neovascularization; macular degeneration; peripheral vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
frontotemporal lobar degeneration Gene Set From GAD Gene-Disease Associations genes associated with the disease frontotemporal lobar degeneration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.
degeneration Gene Set From GeneRIF Biological Term Annotations genes co-occuring with the biological term degeneration in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.
Age-related macular degeneration (CNV vs. GA) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Age-related macular degeneration (CNV vs. GA) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Age-related macular degeneration (GA) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Age-related macular degeneration (GA) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Age-related macular degeneration (CNV) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Age-related macular degeneration (CNV) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Age-related macular degeneration (wet) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Age-related macular degeneration (wet) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Age-related macular degeneration (extreme sampling) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Age-related macular degeneration (extreme sampling) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
Disc degeneration (lumbar) Gene Set From GWAS Catalog SNP-Phenotype Associations genes associated with the Disc degeneration (lumbar) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.
macular degeneration Gene Set From GWASdb SNP-Disease Associations genes associated with the disease macular degeneration in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
age related macular degeneration Gene Set From GWASdb SNP-Disease Associations genes associated with the disease age related macular degeneration in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
retinal degeneration Gene Set From GWASdb SNP-Disease Associations genes associated with the disease retinal degeneration in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
degeneration of macula and posterior pole Gene Set From GWASdb SNP-Disease Associations genes associated with the disease degeneration of macula and posterior pole in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.
age-related macular degeneration Gene Set From GWASdb SNP-Phenotype Associations genes associated with the age-related macular degeneration phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
macular degeneration Gene Set From GWASdb SNP-Phenotype Associations genes associated with the macular degeneration phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
intervertebral disc degeneration Gene Set From GWASdb SNP-Phenotype Associations genes associated with the intervertebral disc degeneration phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
atrophy/degeneration affecting the central nervous system Gene Set From GWASdb SNP-Phenotype Associations genes associated with the atrophy/degeneration affecting the central nervous system phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.
atrophy/degeneration affecting the central nervous system Gene Set From HPO Gene-Disease Associations genes associated with the atrophy/degeneration affecting the central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
dorsal column degeneration Gene Set From HPO Gene-Disease Associations genes associated with the dorsal column degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy/degeneration involving the corticospinal tracts Gene Set From HPO Gene-Disease Associations genes associated with the atrophy/degeneration involving the corticospinal tracts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive cone degeneration Gene Set From HPO Gene-Disease Associations genes associated with the progressive cone degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
choroidoretinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the choroidoretinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripheral vitreoretinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the peripheral vitreoretinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pallidal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the pallidal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
tapetoretinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the tapetoretinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
retinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the retinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cystoid macular degeneration Gene Set From HPO Gene-Disease Associations genes associated with the cystoid macular degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
spinocerebellar tract degeneration Gene Set From HPO Gene-Disease Associations genes associated with the spinocerebellar tract degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
macular degeneration Gene Set From HPO Gene-Disease Associations genes associated with the macular degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cerebral degeneration Gene Set From HPO Gene-Disease Associations genes associated with the cerebral degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
axonal degeneration/regeneration Gene Set From HPO Gene-Disease Associations genes associated with the axonal degeneration/regeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cochlear degeneration Gene Set From HPO Gene-Disease Associations genes associated with the cochlear degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
late-onset spinocerebellar degeneration Gene Set From HPO Gene-Disease Associations genes associated with the late-onset spinocerebellar degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy/degeneration affecting the cerebrum Gene Set From HPO Gene-Disease Associations genes associated with the atrophy/degeneration affecting the cerebrum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy/degeneration affecting the brainstem Gene Set From HPO Gene-Disease Associations genes associated with the atrophy/degeneration affecting the brainstem phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy/degeneration involving the caudate nucleus Gene Set From HPO Gene-Disease Associations genes associated with the atrophy/degeneration involving the caudate nucleus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
vitreoretinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the vitreoretinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
pigmentary retinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the pigmentary retinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
peripheral axonal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the peripheral axonal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
age-related macular degeneration Gene Set From HPO Gene-Disease Associations genes associated with the age-related macular degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
atrophy/degeneration involving the spinal cord Gene Set From HPO Gene-Disease Associations genes associated with the atrophy/degeneration involving the spinal cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
choroidal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the choroidal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
granulovacuolar degeneration Gene Set From HPO Gene-Disease Associations genes associated with the granulovacuolar degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
honeycomb retinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the honeycomb retinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
corneal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the corneal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
degeneration of the lateral corticospinal tracts Gene Set From HPO Gene-Disease Associations genes associated with the degeneration of the lateral corticospinal tracts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
cystic retinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the cystic retinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
central nervous system degeneration Gene Set From HPO Gene-Disease Associations genes associated with the central nervous system degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
intervertebral disc degeneration Gene Set From HPO Gene-Disease Associations genes associated with the intervertebral disc degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
degeneration of anterior horn cells Gene Set From HPO Gene-Disease Associations genes associated with the degeneration of anterior horn cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
progressive retinal degeneration Gene Set From HPO Gene-Disease Associations genes associated with the progressive retinal degeneration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
Macular Degeneration Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Macular Degeneration phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Wet Macular Degeneration Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Wet Macular Degeneration phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Frontotemporal Lobar Degeneration Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Frontotemporal Lobar Degeneration phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Retinal Degeneration Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Retinal Degeneration phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Nerve Degeneration Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Nerve Degeneration phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Intervertebral Disk Degeneration Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Intervertebral Disk Degeneration phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Hepatolenticular Degeneration Gene Set From HuGE Navigator Gene-Phenotype Associations genes associated with the Hepatolenticular Degeneration phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.
Progressive rod-cone degeneration protein Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Progressive rod-cone degeneration protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.
Retinal degeneration protein 3 Gene Set From InterPro Predicted Protein Domain Annotations proteins predicted to have the Retinal degeneration protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.
vestibular hair cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the vestibular hair cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
neural tube degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the neural tube degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
stria vascularis degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the stria vascularis degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
epididymis epithelium degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the epididymis epithelium degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cochlear inner hair cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cochlear inner hair cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cochlear hair cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cochlear hair cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
inner cell mass degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the inner cell mass degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
optic nerve degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the optic nerve degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
spiral ligament degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the spiral ligament degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
amacrine cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the amacrine cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
muscle degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the muscle degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
wolffian duct degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the wolffian duct degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
liver degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the liver degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
myocardial fiber degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the myocardial fiber degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
embryonic epiblast cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the embryonic epiblast cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
neuron degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the neuron degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
intervertebral disk degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the intervertebral disk degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
mullerian duct degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the mullerian duct degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
purkinje cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the purkinje cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cervical vertebrae degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cervical vertebrae degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
oocyte degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the oocyte degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
hair follicle degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the hair follicle degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
photoreceptor inner segment degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the photoreceptor inner segment degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
heart right ventricle degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the heart right ventricle degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
kidney degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the kidney degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ovary degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ovary degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
abnormal wallerian degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the abnormal wallerian degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
pillar cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the pillar cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
vestibular saccular degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the vestibular saccular degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal outer nuclear layer degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal outer nuclear layer degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cochlear degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cochlear degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
type ii spiral ligament fibrocyte degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the type ii spiral ligament fibrocyte degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal rod cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal rod cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal cone cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal cone cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
vestibular ganglion degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the vestibular ganglion degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
photoreceptor outer segment degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the photoreceptor outer segment degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
vestibular dark cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the vestibular dark cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cerebral cortex pyramidal cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cerebral cortex pyramidal cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
dorsal root ganglion degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the dorsal root ganglion degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
hippocampal neuron degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the hippocampal neuron degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
degeneration of organ of corti supporting cells Gene Set From MPO Gene-Phenotype Associations gene mutations causing the degeneration of organ of corti supporting cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal ganglion cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal ganglion cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
axon degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the axon degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
type i spiral ligament fibrocyte degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the type i spiral ligament fibrocyte degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cardiac muscle degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cardiac muscle degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
utricular macular degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the utricular macular degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
vestibular saccular macula degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the vestibular saccular macula degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
utricular degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the utricular degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
notochord degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the notochord degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
skeletal muscle degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the skeletal muscle degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
type iv spiral ligament fibrocyte degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the type iv spiral ligament fibrocyte degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
hippocampus pyramidal cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the hippocampus pyramidal cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
retinal photoreceptor degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the retinal photoreceptor degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
motor neuron degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the motor neuron degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
skeletal muscle fiber degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the skeletal muscle fiber degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cochlear ganglion degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cochlear ganglion degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
peripheral nervous system degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the peripheral nervous system degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
spinal cord degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the spinal cord degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
seminiferous tubule degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the seminiferous tubule degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
trophectoderm cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the trophectoderm cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
cochlear outer hair cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the cochlear outer hair cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
ameloblast degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the ameloblast degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
superior cervical ganglion degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the superior cervical ganglion degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
deiters cell degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the deiters cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
slow wallerian degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the slow wallerian degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
organ of corti degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the organ of corti degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
type iii spiral ligament fibrocyte degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the type iii spiral ligament fibrocyte degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
epididymis degeneration Gene Set From MPO Gene-Phenotype Associations gene mutations causing the epididymis degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.
mental retardation, severe, with spasticity and tapetoretinal degeneration Gene Set From OMIM Gene-Disease Associations genes associated with the mental retardation, severe, with spasticity and tapetoretinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset.
striatal degeneration, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the striatal degeneration, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
macular degeneration, early-onset Gene Set From OMIM Gene-Disease Associations genes associated with the macular degeneration, early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.
{lumbar disc degeneration} Gene Set From OMIM Gene-Disease Associations genes associated with the {lumbar disc degeneration} phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal degeneration, late-onset, autosomal dominant Gene Set From OMIM Gene-Disease Associations genes associated with the retinal degeneration, late-onset, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset.
macular degeneration, age-related, 15, suscepbitility to Gene Set From OMIM Gene-Disease Associations genes associated with the macular degeneration, age-related, 15, suscepbitility to phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 14, reduced risk of} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 14, reduced risk of} phenotype from the curated OMIM Gene-Disease Associations dataset.
myopia, high, with cataract and vitreoretinal degeneration Gene Set From OMIM Gene-Disease Associations genes associated with the myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, neovascular type} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, neovascular type} phenotype from the curated OMIM Gene-Disease Associations dataset.
snowflake vitreoretinal degeneration Gene Set From OMIM Gene-Disease Associations genes associated with the snowflake vitreoretinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 2} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.
frontotemporal lobar degeneration, tardbp-related Gene Set From OMIM Gene-Disease Associations genes associated with the frontotemporal lobar degeneration, tardbp-related phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 4} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 4} phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 12} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 12} phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, susceptibility to 5} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, susceptibility to 5} phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 10} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 10} phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 8} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 8} phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, reduced risk of} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, reduced risk of} phenotype from the curated OMIM Gene-Disease Associations dataset.
{?macular degeneration, age-related} Gene Set From OMIM Gene-Disease Associations genes associated with the {?macular degeneration, age-related} phenotype from the curated OMIM Gene-Disease Associations dataset.
doyne honeycomb degeneration of retina Gene Set From OMIM Gene-Disease Associations genes associated with the doyne honeycomb degeneration of retina phenotype from the curated OMIM Gene-Disease Associations dataset.
macular degeneration, age-related, 11 Gene Set From OMIM Gene-Disease Associations genes associated with the macular degeneration, age-related, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular degeneration, age-related, 3 Gene Set From OMIM Gene-Disease Associations genes associated with the macular degeneration, age-related, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular degeneration, age-related, 6 Gene Set From OMIM Gene-Disease Associations genes associated with the macular degeneration, age-related, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.
macular degeneration, juvenile Gene Set From OMIM Gene-Disease Associations genes associated with the macular degeneration, juvenile phenotype from the curated OMIM Gene-Disease Associations dataset.
macular degeneration, x-linked atrophic Gene Set From OMIM Gene-Disease Associations genes associated with the macular degeneration, x-linked atrophic phenotype from the curated OMIM Gene-Disease Associations dataset.
frontotemporal lobar degeneration with ubiquitin-positive inclusions Gene Set From OMIM Gene-Disease Associations genes associated with the frontotemporal lobar degeneration with ubiquitin-positive inclusions phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 1} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.
retinal degeneration, autosomal recessive, clumped pigment type Gene Set From OMIM Gene-Disease Associations genes associated with the retinal degeneration, autosomal recessive, clumped pigment type phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 7} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 7} phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 13, susceptibility to} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 13, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.
{macular degeneration, age-related, 9} Gene Set From OMIM Gene-Disease Associations genes associated with the {macular degeneration, age-related, 9} phenotype from the curated OMIM Gene-Disease Associations dataset.
striatonigral degeneration, infantile Gene Set From OMIM Gene-Disease Associations genes associated with the striatonigral degeneration, infantile phenotype from the curated OMIM Gene-Disease Associations dataset.
Hepatolenticular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hepatolenticular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Age Related Macular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Age Related Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Exudative Age-Related Macular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Exudative Age-Related Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Exudative Macular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Exudative Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Juvenile Macular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Juvenile Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Macular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Photoreceptor Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Photoreceptor Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vitreoretinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vitreoretinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Degeneration Of Lumbar Intervertebral Disc Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Degeneration Of Lumbar Intervertebral Disc in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Intervertebral Disc Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Intervertebral Disc Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pallidopontonigral Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pallidopontonigral Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Muscle Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Muscle Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Wet Age-Related Macular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Wet Age-Related Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Chorioretinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Chorioretinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Degeneration Of The Striatum Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Degeneration Of The Striatum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Stiatonigral Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Stiatonigral Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Frontotemporal Lobar Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Frontotemporal Lobar Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Meniscal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Meniscal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Late-Onset Retinal Degeneration (Disorder) Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Late-Onset Retinal Degeneration (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypoprebetalipoproteinemia, Acanthocytosis, Retinitis Pigmentosa, And Pallidal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Corticobasal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Corticobasal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinocerebellar Tract Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinocerebellar Tract Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vascular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vascular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Striatonigral Degeneration, Infantile, Mitochondrial Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Striatonigral Degeneration, Infantile, Mitochondrial in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Atrophy/Degeneration Affecting The Brainstem Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Atrophy/Degeneration Affecting The Brainstem in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nervous System--Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nervous System--Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pallidoluysian Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pallidoluysian Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Degeneration Of Spine Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Degeneration Of Spine in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cystoid Macular Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cystoid Macular Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Facet Joint Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Facet Joint Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Snowflake Vitreoretinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Snowflake Vitreoretinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Glaucomatous Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Glaucomatous Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Nonexudative Age-Related Macular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Nonexudative Age-Related Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hyaloideoretinal Degeneration Of Wagner Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hyaloideoretinal Degeneration Of Wagner in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Vitreous Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Vitreous Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Lattice Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Lattice Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Corneal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Corneal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Striatonigral Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Striatonigral Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Basal Ganglion Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Basal Ganglion Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Age-Related Macular Degeneration Type 11 Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Age-Related Macular Degeneration Type 11 in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Reticular Pigmentary Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Reticular Pigmentary Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Myopic Macular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Myopic Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Mptp-Induced Degeneration Of The Striatum Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Mptp-Induced Degeneration Of The Striatum in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cns Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cns Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Cochleosaccular Degeneration Of The Inner Ear And Progressive Cataracts Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Cochleosaccular Degeneration Of The Inner Ear And Progressive Cataracts in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Arteriovascular Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Arteriovascular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Pallidal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Pallidal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Striatal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Striatal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Striatal Degeneration, Autosomal Dominant Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Striatal Degeneration, Autosomal Dominant in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Hypertrophic Olivary Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Hypertrophic Olivary Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Peripheral Retinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Peripheral Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Corticostriatal-Spinal Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Corticostriatal-Spinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Lumbar Spine Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Lumbar Spine Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Spinal Cord Degeneration Gene Set From DisGeNET Gene-Disease Associations genes associated with the disease Spinal Cord Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
Neurofibrillary Degeneration (Morphologic Abnormality) Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Neurofibrillary Degeneration (Morphologic Abnormality) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Nerve Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Nerve Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Macular Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Central Nervous System Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Central Nervous System Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy/Degeneration Involving The Caudate Nucleus Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Involving The Caudate Nucleus in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Pigmentary Iris Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Pigmentary Iris Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Axonal Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Axonal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peripheral Axonal Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Axonal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Degeneration Of Anterior Horn Cells Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Degeneration Of Anterior Horn Cells in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Degeneration Of The Lateral Corticospinal Tracts Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Degeneration Of The Lateral Corticospinal Tracts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Dry Age-Related Macular Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dry Age-Related Macular Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Dorsal Column Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dorsal Column Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy/Degeneration Involving The Corticospinal Tracts Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Involving The Corticospinal Tracts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retrograde Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retrograde Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Wallerian Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Wallerian Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Retinal Pigmentary Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Retinal Pigmentary Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Cochlear Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Cochlear Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Late-Onset Spinocerebellar Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Late-Onset Spinocerebellar Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Axonal Degeneration/Regeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Axonal Degeneration/Regeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Granulovacuolar Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Granulovacuolar Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peripheral Vitreoretinal Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Vitreoretinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy/Degeneration Involving The Spinal Cord Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Involving The Spinal Cord in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Peripheral Cystoid Retinal Degeneration Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Peripheral Cystoid Retinal Degeneration in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy/Degeneration Affecting The Central Nervous System Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Affecting The Central Nervous System in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
Atrophy/Degeneration Affecting The Cerebrum Gene Set From DisGeNET Gene-Phenotype Associations genes associated with the phenotype Atrophy/Degeneration Affecting The Cerebrum in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset.
oocyte degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the oocyte degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
notochord degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the notochord degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
epididymis degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the epididymis degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cochlear ganglion degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cochlear ganglion degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
vestibular hair cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the vestibular hair cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Purkinje cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the Purkinje cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cochlear hair cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cochlear hair cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cochlear inner hair cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cochlear inner hair cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cochlear outer hair cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cochlear outer hair cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
organ of Corti degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the organ of Corti degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
degeneration of organ of Corti supporting cells Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the degeneration of organ of Corti supporting cells phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina photoreceptor degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina photoreceptor degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina outer nuclear layer degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina outer nuclear layer degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
photoreceptor outer segment degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the photoreceptor outer segment degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
seminiferous tubule degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the seminiferous tubule degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
neuron degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the neuron degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
slow Wallerian degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the slow Wallerian degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
muscle degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the muscle degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
ameloblast degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ameloblast degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
ovary degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the ovary degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
vestibular ganglion degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the vestibular ganglion degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
motor neuron degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the motor neuron degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
vestibular saccular macula degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the vestibular saccular macula degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
pillar cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the pillar cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
hippocampal neuron degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the hippocampal neuron degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina ganglion cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina ganglion cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
inner cell mass degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the inner cell mass degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
kidney degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the kidney degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
myocardial fiber degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the myocardial fiber degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Deiters cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the Deiters cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
utricular macular degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the utricular macular degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
liver degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the liver degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
vestibular dark cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the vestibular dark cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
optic nerve degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the optic nerve degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Wolffian duct degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the Wolffian duct degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
axon degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the axon degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
amacrine cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the amacrine cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
stria vascularis degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the stria vascularis degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
epididymis epithelium degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the epididymis epithelium degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
testis degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the testis degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
spiral ligament degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the spiral ligament degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
hair follicle degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the hair follicle degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
superior cervical ganglion degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the superior cervical ganglion degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina cone cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina cone cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
skeletal muscle fiber degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the skeletal muscle fiber degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
skeletal muscle degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the skeletal muscle degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cardiac muscle degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cardiac muscle degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
facial muscle degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the facial muscle degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
intervertebral disk degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the intervertebral disk degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Mullerian duct degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the Mullerian duct degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
peripheral nervous system degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the peripheral nervous system degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
type I spiral ligament fibrocyte degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the type I spiral ligament fibrocyte degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
type III spiral ligament fibrocyte degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the type III spiral ligament fibrocyte degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
spinal cord degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the spinal cord degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cochlear degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cochlear degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
type II spiral ligament fibrocyte degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the type II spiral ligament fibrocyte degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
type IV spiral ligament fibrocyte degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the type IV spiral ligament fibrocyte degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
trophectoderm cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the trophectoderm cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
hippocampus pyramidal cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the hippocampus pyramidal cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina rod cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina rod cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
heart right ventricle degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the heart right ventricle degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
embryonic epiblast cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the embryonic epiblast cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cervical vertebrae degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cervical vertebrae degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
vestibular saccular degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the vestibular saccular degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
utricular degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the utricular degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
neural tube degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the neural tube degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
seminal vesicle epithelium degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the seminal vesicle epithelium degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
photoreceptor inner segment degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the photoreceptor inner segment degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
abnormal Wallerian degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal Wallerian degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
cerebral cortex pyramidal cell degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the cerebral cortex pyramidal cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
gastric gland degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the gastric gland degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
nasal gland degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the nasal gland degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
salivary gland degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the salivary gland degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
pancreas degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the pancreas degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
dorsal root ganglion degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the dorsal root ganglion degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
retina macular degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the retina macular degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Meibomian gland degeneration Gene Set From MGI Mouse Phenotype Associations 2023 gene mutations causing the Meibomian gland degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.
Retinal degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Retinal degeneration from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Degeneration of macula and posterior pole Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Degeneration of macula and posterior pole from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Age related macular degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Age related macular degeneration from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Macular degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Macular degeneration from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Cerebral degeneration Gene Set From DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Cerebral degeneration from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset.
Age related macular degeneration Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Age related macular degeneration in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Degeneration of macula and posterior pole Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Degeneration of macula and posterior pole in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Macular degeneration Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Macular degeneration in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal degeneration Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Retinal degeneration in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Kuhnt-Junius degeneration Gene Set From DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Kuhnt-Junius degeneration in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 10 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 10 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Macular degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Macular degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Degeneration of macula and posterior pole Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Degeneration of macula and posterior pole in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cerebral degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cerebral degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Corneal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Corneal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Retinal lattice degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Retinal lattice degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Peripheral retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Peripheral retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
late-onset retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease late-onset retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
X-linked atrophic macular degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease X-linked atrophic macular degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Kuhnt-Junius degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Kuhnt-Junius degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 12 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 12 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Striatonigral degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Striatonigral degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Conjunctival degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Conjunctival degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 1 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Corticobasal degeneration syndrome Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Corticobasal degeneration syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Pulp degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pulp degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 2 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Snowflake vitreoretinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Snowflake vitreoretinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 8 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 8 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 15 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 15 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 7 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 7 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 13 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 13 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Cobblestone retinal degeneration Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Cobblestone retinal degeneration in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 9 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 9 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 14 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 14 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 4 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 4 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration 11 Gene Set From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Age related macular degeneration 11 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
Age related macular degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Age related macular degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Late-onset retinal degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Late-onset retinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Spongy degeneration of central nervous system Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Spongy degeneration of central nervous system phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Pigmentary pallidal degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Pigmentary pallidal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Macular degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Macular degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Age-related macular degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Age-related macular degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Snowflake vitreoretinal degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Snowflake vitreoretinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Trichomegaly-retina pigmentary degeneration-dwarfism syndrome Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Trichomegaly-retina pigmentary degeneration-dwarfism syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Retinal degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Retinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
GRN-related frontotemporal lobar degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the GRN-related frontotemporal lobar degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Skeletal dysplasia and progressive central nervous system degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Skeletal dysplasia and progressive central nervous system degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Striatal degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Striatal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Lattice retinal degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Lattice retinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Striatonigral degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Striatonigral degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Helicoid peripapillary chorioretinal degeneration Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Helicoid peripapillary chorioretinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Atrophy/Degeneration affecting the central nervous system Gene Set From ClinVar Gene-Phenotype Associations 2025 genes associated with the Atrophy/Degeneration affecting the central nervous system phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
Age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Corticobasal degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Corticobasal degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Advanced age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Advanced age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Exudative age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Exudative age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related macular degeneration (SNP x mitochondrial G12771A interaction) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related macular degeneration (SNP x mitochondrial G12771A interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Disc degeneration (lumbar) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Disc degeneration (lumbar) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Early age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Early age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to ranibizumab in age-related macular degeneration (exudative) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to ranibizumab in age-related macular degeneration (exudative) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related macular degeneration (extreme sampling) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related macular degeneration (extreme sampling) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related macular degeneration (wet) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related macular degeneration (wet) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related macular degeneration (choroidal neovascularisation) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related macular degeneration (choroidal neovascularisation) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related macular degeneration (geographic atrophy) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related macular degeneration (geographic atrophy) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related macular degeneration (CNV vs. GA) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related macular degeneration (CNV vs. GA) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Laterality in neovascular age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Laterality in neovascular age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Age-related macular degeneration (MTAG) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Age-related macular degeneration (MTAG) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Neovascular age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Neovascular age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Disease progression in age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Disease progression in age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Disease progression in age-related macular degeneration (adjusted for baseline) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Disease progression in age-related macular degeneration (adjusted for baseline) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Disease progression to geographic atrophy form in age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Disease progression to geographic atrophy form in age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Disease progression to choroidal neovascularization form in age-related macular degeneration Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Disease progression to choroidal neovascularization form in age-related macular degeneration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.
Response to antioxidants and zinc in age-related macular degeneration (disease progression) Gene Set From GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Response to antioxidants and zinc in age-related macular degeneration (disease progression) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset.

Harmonizome 3.0

LOC101060399 Gene

CDR2L Gene

CDR3 Gene

CDR2 Gene

CDR1 Gene

CLA3 Gene

RD3L Gene

PRPH2 Gene

PRCD Gene

RD3 Gene

CLAM Gene

CCCSX Gene

CHMRQ Gene

ATCAY Gene

Cerebellar Degeneration, Subacute Gene Set

Subacute Combined Degeneration Gene Set

CEREBELLAR DEGENERATION-RELATED AUTOANTIGEN 3 Gene Set

primary cerebellar degeneration Gene Set

Cerebellar degeneration-related protein 2 Gene Set

infantile cerebellar-retinal degeneration Gene Set

Cerebellar Degeneration Gene Set

Infantile Cerebellar-Retinal Degeneration Gene Set

Progressive Cerebellar Degeneration Gene Set

Paraneoplastic Cerebellar Degeneration Gene Set

Paraneoplastic Cerebellar Degeneration, Anti-Yo-Associated Gene Set

Primary cerebellar degeneration Gene Set

Infantile cerebellar-retinal degeneration Gene Set

Infantile cerebellar-retinal degeneration Gene Set

macular degeneration; nephritis, hereditary; retinal degeneration; retinal drusen Gene Set

eye diseases, hereditary; macular degeneration; retinal degeneration Gene Set

Subacute neuronopathic Gaucher's disease Gene Set

subacute glomerulonephritis Gene Set

subacute bacterial endocarditis Gene Set

subacute lymphocytic thyroiditis Gene Set

subacute thyroiditis Gene Set

subacute sclerosing panencephalitis Gene Set

subacute myeloid leukemia Gene Set

subacute g(m2) gangliosidosis Gene Set

thryoiditis, subacute granulomatous Gene Set

dawson's inclusion body encephalitis; subacute sclerosing panencephalitis Gene Set

panencephalitis, subacute sclerosing Gene Set

subacute sclerosing panencephalitis Gene Set

subacute Gene Set

subacute progressive viral hepatitis Gene Set

Thyroiditis, Subacute Gene Set

Subacute Sclerosing Panencephalitis Gene Set

Subacute Sclerosing Panencephalitis Gene Set

Rasmussen Subacute Encephalitis Gene Set

Subacute Bacterial Endocarditis Gene Set

Necrotizing Encephalopathy, Infantile Subacute, Of Leigh Gene Set

Subacute Thyroiditis Gene Set

Subacute Cutaneous Lupus Gene Set

Acute And Subacute Liver Necrosis (Disorder) Gene Set

Subacute Dermatitis Gene Set

Subacute Hepatic Necrosis Gene Set

Subacute Adenoviral Encephalitis Gene Set

Lupus Erythematosus, Subacute Gene Set

Atypical Subacute Thyroiditis Gene Set

Subacute Necrotising Encephalomyopathy Gene Set

Subacute Progressive Viral Hepatitis Gene Set

Subacute sclerosing panencephalitis Gene Set

Subacute thyroiditis Gene Set

Subacute bacterial endocarditis Gene Set

Subacute lymphocytic thyroiditis Gene Set

Subacute leukemia Gene Set

Subacute delirium Gene Set

Subacute glomerulonephritis Gene Set

cerebellar hemisphere Gene Set

dorsolateral (non-cerebellar) part of isA Gene Set

mantle zone of cerebellar vermis Gene Set

cerebellar white matter Gene Set

white matter of cerebellar vermis Gene Set

lateral (dentate) cerebellar nucleus Gene Set

cerebellar vermis Gene Set

cerebellar nuclei of CbH Gene Set

Cerebellar nuclei Gene Set

cortex of cerebellar hemisphere Gene Set

intermediate (interpositus) cerebellar nucleus Gene Set

cortex of cerebellar vermis Gene Set