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- Bbc7421dddb0e924b55be80a7833922cd hasDbXref "Orphanet:75501" @default.
- Bbc7421dddb0e924b55be80a7833922cd type Axiom @default.
- Bbc7421dddb0e924b55be80a7833922cd annotatedProperty IAO_0000115 @default.
- Bbc7421dddb0e924b55be80a7833922cd annotatedSource MONDO_0009158 @default.
- Bbc7421dddb0e924b55be80a7833922cd annotatedTarget "Ehlers-Danlos syndromes (EDS) form a heterogeneous group of inherited connective tissue disorders characterized by variable joint hypermobility and cutaneous hyperextensibility. Type X is distinguished by platelet dysfunction associated with a fibronectin abnormality. Type X EDS has been described in only one family so far. Age of onset is about 13-25 years. Transmission is autosomal recessive." @default.