autosomal dominant chondrodysplasia punctata Disease Ontology Browser

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Disease Ontology Browser

autosomal dominant chondrodysplasia punctata (DOID:0060293)
Alliance: disease page
Alt IDs: OMIM:118650, OMIM:118651, OMIM:602497, ICD10CM:Q77.3, ORDO:79344
Definition: A chondrodysplasia punctata that is characterized by abnormal facies and stippling of the limbs, associated with vitamin K-related teratogenicity, has_material_basis_in autosomal dominant inheritance.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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