autosomal dominant chondrodysplasia punctata

Summary

DOID:0060293 - autosomal dominant chondrodysplasia punctata

Disease Ontology 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.

Synonyms:

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

:

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0007321 - autosomal dominant chondrodysplasia punctata

MONDO:0007321 - autosomal dominant chondrodysplasia punctata

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), chondrodysplasia punctata (is_a)