MeSH Browser

MeSH Supplementary: Oculodentodigital Dysplasia, Autosomal Recessive
Unique ID: C567605
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567605
Entry Term(s): Oculodentoosseous Dysplasia, Autosomal Recessive
Registry Numbers: 0
Heading Mapped to: *Eye Abnormalities; *Syndactyly; *Tooth Abnormalities; Connexin 43 / deficiency; *Craniofacial Abnormalities
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Oculodentodigital Dysplasia, Autosomal Recessive MeSH Supplementary Concept Data 2025