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Human Disease

autosomal dominant chondrodysplasia punctata

Term ID
DOID:0060293
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. https://www.omim.org/entry/118650
References
Ontology
Human Disease   ( DOID:0060293 )
Relationships
is a type of
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Genes Involved
Zebrafish Models