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DO Term : Fanconi anemia complementation group V [DOID:0111080] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Fanconi anemia that has_material_basis_in homozygous mutation in the MAD2L2 gene on chromosome 1p36.

synonyms:
617243,
FANCV,
OMIM:617243

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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