Disease #01270 (CDD (dysplasia, craniodiaphyseal, autosomal dominant (CDD), OMIM:122860)

Official abbreviation CDD
Name dysplasia, craniodiaphyseal, autosomal dominant (CDD
OMIM ID 122860
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 SOST
Associated tissues -
Disease features -
Remarks -