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Fanconi Anemia Complementation Group F (MONDO:0011325)

Fanconi anemia caused by mutations of the FANCF gene. This gene encodes a polypeptide with homology to the prokaryotic RNA-binding protein ROM.

Overview

Category

Ontology ID

Internal:12438

Synonyms

FANCF

Fanconi Anemia, complementation group type F

Fanconi anaemia complementation group type F

Fanconi anemia complementation group F

Fanconi anemia complementation group type F

Fanconi anemia, complementation group F

Mapped terms

DOID:0111088

GARD:0015355

MEDGEN:854016

NCIT:C125707

OMIM:603467

UMLS:C3469526

Child terms

Unknown children.