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Fanconi Anemia Complementation Group B (MONDO:0010351)

Fanconi anemia caused by mutations of the FANCB gene. This gene encodes the protein for complementation group B.

Overview

Category

Ontology ID

Internal:11518

Synonyms

FA2

FACB

FANCB

Fanconi Anemia, complementation group type B

Fanconi anaemia complementation group type B

Fanconi anemia complementation group B

Fanconi anemia complementation group type B

Fanconi anemia, complementation group B, X-linked recessive

Fanconi anemia, complementation group B

Fanconi pancytopenia, type 2

Mapped terms

DOID:0111098

GARD:0015257

MEDGEN:336901

MESH:C564497

NCIT:C125703

OMIM:300514

UMLS:C1845292

Child terms

Unknown children.