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Ellis-van Creveld syndrome

Disease Summary
Associated Targets (4)
Tbio

3

Tchem

1


GARD Rare
Mondo Description Ellis-van Creveld syndrome (EVC) is a skeletal and ectoderlam dysplasia characterized by a tetrad of short stature, postaxial polydactyly, ectodermal dysplasia, and congenital heart defects.
Uniprot Description An autosomal recessive condition characterized by the clinical tetrad of chondrodystrophy, polydactyly, ectodermal dysplasia and cardiac anomalies. Patients manifest short-limb dwarfism, short ribs, postaxial polydactyly, and dysplastic nails and teeth. Congenital heart defects, most commonly an atrioventricular septal defect, are observed in 60% of affected individuals.
Mondo Term and Equivalent IDs
MONDO:0009162:  Ellis-van Creveld syndrome
GARD:0001301: 
ICD9:756.55: 
MESH:D004613: 
NCIT:C84684: 
Orphanet:289: 
SCTID:62501005: 
UMLS:C0013903: 
UMLS:CN239258: