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DO Term : autosomal dominant chondrodysplasia punctata [DOID:0060293] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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:
  • ICD10CM:Q77.3,
  • OMIM:118650,
  • ORDO:79344,
  • OMIM:602497,
  • 118651,
  • 602497,
  • OMIM:118651,
  • 118650
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents