Craniometadiaphyseal osteosclerosis with hip dysplasia

Preferred Label : Craniometadiaphyseal osteosclerosis with hip dysplasia;

Symbol : CMDOH;

Type : Phenotype, molecular basis known;

Prefixed ID : #620558;

Détails

Origin ID

620558;

UMLS CUI

C5882710;

Genes related to phenotype
- Axis inhibitor 1 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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