Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B9a3089a6bd8faada608b6ce40ee7bda7> ?p ?o ?g. }
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- B9a3089a6bd8faada608b6ce40ee7bda7 hasDbXref "Orphanet:276280" @default.
- B9a3089a6bd8faada608b6ce40ee7bda7 hasDbXref "https://orcid.org/0000-0001-5208-3432" @default.
- B9a3089a6bd8faada608b6ce40ee7bda7 type Axiom @default.
- B9a3089a6bd8faada608b6ce40ee7bda7 annotatedProperty IAO_0000115 @default.
- B9a3089a6bd8faada608b6ce40ee7bda7 annotatedSource MONDO_0017177 @default.
- B9a3089a6bd8faada608b6ce40ee7bda7 annotatedTarget "A rare, genetic overgrowth syndrome characterized by non- progressive, asymmetrical, moderate hemihyperplasia (frequently affecting the limbs) associated with slow growing, painless, multiple, recurrent, subcutaneous lipomatous masses distributed throughout entire body (in particular back, torso, extremities, fingers, axillae). Superficial vascular malformations may also be associated. Increased risk of intra-abdominal embryonal malignancies may be associated." @default.