You are using an outdated browser. Please upgrade your browser to improve your experience.

EEC syndrome

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description EEC syndrome is a genetic developmental disorder characterized by ectrodactyly, ectodermal dysplasia, and orofacial clefts (cleft lip/palate).
Disease Ontology Description An autosomal dominant disease characterized by ectrodactyly, ectodermal dysplasia, and orofacial clefts (cleft lip-palate).
Mondo Term and Equivalent IDs
MONDO:0010004:  EEC syndrome
DC:0000689: 
GARD:0002076: 
MESH:C536189: 
NCIT:C148261: 
Orphanet:1896: 
SCTID:39788007: 
UMLS:C0406704: 
UMLS:CN776907: