Ehlers-Danlos syndrome, fibronectinemic type
MONDO:0009158Mondo
Findings
No curated finding names Ehlers-Danlos syndrome, fibronectinemic type yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
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.
Definition from the Mondo Disease Ontology (MONDO:0009158), read 2026-09-29. CC BY 4.0.
Where it sits
Other names
4 names
Resolves to: Ehlers-Danlos syndrome, fibronectinemic type
- Also called
- EDS XEhlers-Danlos syndrome type 10Ehlers-Danlos syndrome with platelet dysfunction from fibronectin abnormalityEhlers-Danlos syndrome, fibronectin-deficient