Terminology Service for NFDI4Health

autosomal dominant chondrodysplasia punctata

Go to external page http://purl.obolibrary.org/obo/DOID_0060293


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. [ http://purl.obolibrary.org/obo/ECO_0007636 ]

Term info

Label

autosomal dominant chondrodysplasia punctata

database cross reference
Subsets

DO_rare_slim

comment

NT MGI.

created by

emitraka

creation date

2015-02-05T16:49:46Z

has obo namespace

disease_ontology

id

DOID:0060293