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DO Term : X-linked dyskeratosis congenita [DOID:0070025] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A dyskeratosis congenita that has_material_basis_in an X-linked recessive mutation of the DKC1 gene on chromosome Xq28.

synonyms:
Zinsser-Cole-Engman syndrome,
DKCX,
305000,
OMIM:305000

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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