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.