ZFIN Human Disease: autosomal dominant chondrodysplasia punctata

OBO ID: DOID:0060293

OBO ID: DOID:0060293

Term Name:	autosomal dominant chondrodysplasia punctata	Search Ontology:
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:	ICD10CM:Q77.3 OMIM:118650 OMIM:118651 OMIM:602497 ORDO:79344
Ontology:	Human Disease ( DOID:0060293 )

Relationships

is a type of:	autosomal dominant disease chondrodysplasia punctata autosomal dominant disease chondrodysplasia punctata Show first 5 Terms

OTHER autosomal dominant chondrodysplasia punctata PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None