Search
ectrodactyly, ectodermal dysplasia, cleft lip/palate syndrome 3 (EEC3)
Genetics:
- autosomal dominant
- associated with p63 mutations at chromosome 3q27
Clinical manifestations:
- ectrodactyly of hands & feet, ectodermal dysplasia & facial clefting
Related
p63 protein; p53 homolog p63; tumor protein p73-like; p73L; TP63; p51; p40; keratinocyte transcription factor KET; chronic ulcerative stomatitis protein (CUSP, TP73L, KET, p63, P73H)
General
ectrodactyly, ectodermal dysplasia, cleft lip/palate syndrome (EEC syndrome)
Database Correlations
OMIM 604292
References
OMIM :accession 604292