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DO Term : Fanconi anemia complementation group D2 [DOID:0111083] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Fanconi anemia that has_material_basis_in compound heterozygous or homozygous mutation in the FANCD2 gene on chromosome 3p25.

synonyms:
OMIM:227646,
FA4,
Fanconi pancytopenia type 4,
227646,
FANCD2,
FAD2

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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