Disease #01272 (CMDD (dysplasia, craniometaphyseal, autosomal dominant (CMDD)), OMIM:123000)

Official abbreviation CMDD
Name dysplasia, craniometaphyseal, autosomal dominant (CMDD)
OMIM ID 123000
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene ANKH
Associated tissues -
Disease features -
Remarks -