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Results for "htlv-i-associated myelopathy": 2 genes, 24 gene sets

Name

HRES2 Gene

HTLV-1 related endogenous sequence 2

HRES1 Gene

HTLV-1 related endogenous sequence

htlv-i-associated myelopathy Gene Set

From GAD Gene-Disease Associations

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

htlv-i infections; htlv-ii infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease htlv-i infections; htlv-ii infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

htlv-i infections; paraparesis, tropical spastic; spinal cord diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease htlv-i infections; paraparesis, tropical spastic; spinal cord diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

htlv-i infections; leukemia, t-cell Gene Set

From GAD Gene-Disease Associations

genes associated with the disease htlv-i infections; leukemia, t-cell in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

htlv-i infections; spinal cord diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease htlv-i infections; spinal cord diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myelopathy/tropical spastic paraparesis Gene Set

From GAD Gene-Disease Associations

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

htlv-1 infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease htlv-1 infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

htlv-i infections; paraparesis, tropical spastic; tropical spastic paraparesis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease htlv-i infections; paraparesis, tropical spastic; tropical spastic paraparesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

htlv-i infections Gene Set

From GAD Gene-Disease Associations

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

htlv-i infections; paraparesis, tropical spastic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease htlv-i infections; paraparesis, tropical spastic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

htlv Gene Set

From GeneRIF Biological Term Annotations

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

myelopathy Gene Set

From GeneRIF Biological Term Annotations

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

myelopathy Gene Set

From HPO Gene-Disease Associations

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

cervical myelopathy Gene Set

From HPO Gene-Disease Associations

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

HTLV-I Infections Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Cervical Myelopathy Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Cervical Myelopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Cervical Spondylosis With Myelopathy Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Cervical Spondylosis With Myelopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Degenerative Myelopathy Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Degenerative Myelopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Chronic Myelopathy Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Chronic Myelopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Human T-Cell Lymphotrophic Virus, Type I [Htlv-I] Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Human T-Cell Lymphotrophic Virus, Type I [Htlv-I] in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Thoracic Myelopathy Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Thoracic Myelopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Vacuolar Myelopathy Gene Set

From DisGeNET Gene-Disease Associations

genes associated with the disease Vacuolar Myelopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Copper deficiency myelopathy Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Copper deficiency myelopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.

Vascular myelopathy Gene Set

From DISEASES Text-mining Gene-Disease Association Evidence Scores 2025

genes co-occuring with the disease Vascular myelopathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.