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- Bdb7a722f4427005f4d16b9faa1571034 hasDbXref "Orphanet:75501" @default.
- Bdb7a722f4427005f4d16b9faa1571034 type Axiom @default.
- Bdb7a722f4427005f4d16b9faa1571034 annotatedProperty IAO_0000115 @default.
- Bdb7a722f4427005f4d16b9faa1571034 annotatedSource MONDO_0009158 @default.
- Bdb7a722f4427005f4d16b9faa1571034 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.