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- Be5f89744d9da5a3b4407ebfdda71ceb3 hasDbXref "Orphanet:1173" @default.
- Be5f89744d9da5a3b4407ebfdda71ceb3 type Axiom @default.
- Be5f89744d9da5a3b4407ebfdda71ceb3 annotatedProperty IAO_0000115 @default.
- Be5f89744d9da5a3b4407ebfdda71ceb3 annotatedSource MONDO_0008935 @default.
- Be5f89744d9da5a3b4407ebfdda71ceb3 annotatedTarget "Cerebellar ataxia-hypogonadism syndrome is a very rare autosomal recessive neurodegenerative disorder characterized by the combination of progressive cerebellar ataxia with onset from early childhood to the fourth decade, and hypogonadotropic hypogonadism (delayed puberty and lack of secondary sex characteristics). Cerebellar ataxia-hypogonadism syndrome belongs to a clinical continuum of neurodegenerative disorders along with clinically overlapping disorders such as ataxia-hypogonadism-choroidal dystrophy syndrome." @default.