autosomal recessive dyskeratosis congenita 1

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Summary

Literature (0)

DOID:0070015 - autosomal recessive dyskeratosis congenita 1

Disease Ontology Definition:A dyskeratosis congenita that has_material_basis_in an autosomal recessive mutation of the NOLA3 gene on chromosome 15q14.

Synonyms: DKCB1

Echinobase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: nhp2

MIM:

MIM:224230 - dyskeratosis congenita, autosomal recessive, 1; dkcb1

MIM:224230 - dyskeratosis congenita, autosomal recessive, 1; dkcb1

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal recessive disease (is_a), dyskeratosis congenita (is_a)