Term Name: autosomal dominant chondrodysplasia punctata
Synonyms:
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.
Ontology: Human Disease [DOID:0060293]   ( DOID:0060293 )

Relationships
is a type of: autosomal dominant disease chondrodysplasia punctata