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- Bc8bb63cac3d3a2701a9ffd487a06fe5f hasDbXref "Orphanet:398073" @default.
- Bc8bb63cac3d3a2701a9ffd487a06fe5f type Axiom @default.
- Bc8bb63cac3d3a2701a9ffd487a06fe5f annotatedProperty IAO_0000115 @default.
- Bc8bb63cac3d3a2701a9ffd487a06fe5f annotatedSource MONDO_0018354 @default.
- Bc8bb63cac3d3a2701a9ffd487a06fe5f annotatedTarget "Prader-Willi-like syndrome is a rare, genetic, endocrine disease characterized by manifestations of a Prader-Willi syndrome phenotype (including obesity, hyperphagia, hypotonia, psychomotor delay, intellectual disability, small hands/feet, hypogonadism, growth hormone deficiency and characteristic facial features) ocurring in the absence of 15q11-q13 genomic abnormalities." @default.