ZFIN Human Disease: orofaciodigital syndrome X

OBO ID: DOID:0060380

OBO ID: DOID:0060380

Term Name:	orofaciodigital syndrome X	Search Ontology:
Synonyms:	OFD10 orofaciodigital syndrome with fibular aplasia
Definition:	An orofaciodigital syndrome that is characterized by facial, oral and digital deformities as well as radial shortening, fibular agenesis and coalescence of tarsal bones. https://omim.org/entry/165590
References:	ICD10CM:Q87.0 MESH:C563491 OMIM:165590 ORDO:2756
Ontology:	Human Disease ( DOID:0060380 )

Relationships

is a type of:	autosomal dominant disease orofaciodigital syndrome autosomal dominant disease orofaciodigital syndrome Show first 5 Terms

OTHER orofaciodigital syndrome X PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None