MeSH Browser

MeSH Supplementary: Craniometaphyseal Dysplasia, Autosomal Dominant
Unique ID: C565145
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565145
Entry Term(s): Autosomal Dominant Craniometaphyseal Dysplasia; Craniometaphyseal Dysplasia, Jackson Type; Craniometaphyseal dysplasia Jackson type; Craniometaphyseal dysplasia autosomal dominant; Craniometaphyseal dysplasia dominant type
Registry Number: 0
Heading Mapped to: *Craniomandibular Disorders
Frequency: 2
Note: dominant form due to mutation in human homolog of mouse ANKH gene
Date of Entry: 2012/11/05
Revision Date: 2015/08/18

Craniometaphyseal Dysplasia, Autosomal Dominant MeSH Supplementary Concept Data 2024