MeSH Browser

MeSH Supplementary: Omodysplasia 2
Unique ID: C567664
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567664
Entry Term(s): OMOD2; Omodysplasia, Autosomal Dominant
Registry Number: 0
Heading Mapped to: Humerus / *abnormalities; *Osteochondrodysplasias; *Facies; Metacarpal Bones / *abnormalities
Frequency: 3
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Omodysplasia 2 MeSH Supplementary Concept Data 2023