Fanconi anemia complementation group F

Fanconi anemia complementation group F

http://purl.obolibrary.org/obo/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. [ NCIT:C125707 ]

Synonyms: Fanconi anaemia complementation group type F Fanconi Anemia, complementation group type F Fanconi anemia complementation group type F Fanconi anemia complementation group F FANCF

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This is just here as a test because I lose it

Term information

database cross reference

EFO:0009045 (MONDO:equivalentTo)
GARD:15355 (OMIM:603467)
NCIT:C125707 (MONDO:equivalentTo)
DOID:0111088 (MONDO:equivalentTo)
OMIM:603467 (MONDO:equivalentTo)

Subsets

gard_rare, rare, nord_rare, clingen

exactMatch

https://omim.org/entry/603467

http://purl.obolibrary.org/obo/DOID_0111088

http://purl.obolibrary.org/obo/NCIT_C125707

has related synonym

Fanconi anemia, complementation group F

MONDO:0011325

seeAlso

https://search.clinicalgenome.org/kb/conditions/MONDO:0011325

Term relations

Subclass of:

Fanconi anemia