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DO Term : autosomal recessive dyskeratosis congenita 3 [DOID:0070019] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A dyskeratosis congenita that has_material_basis_in an autosomal recessive mutation of the WRAP53 gene on chromosome 17p13.1.
  • synonyms:
  • OMIM:613988,
  • 613988,
  • DKCB3
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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





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