Fanconi anemia complementation group G

Fanconi anemia complementation group G

http://purl.obolibrary.org/obo/MONDO_0013565

Fanconi anemia caused by mutations of the FANCG gene. [ NCIT:C125708 ]

Synonyms: Fanconi anemia complementation group G Fanconi anaemia complementation group type G Fanconi anemia complementation group type G Fanconi Anemia, complementation group type G FANCG

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Term mappings

Preferred root terms

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This is just here as a test because I lose it

Term information

database cross reference

OMIM:614082 (MONDO:equivalentTo)
GARD:15753 (OMIM:614082)
NCIT:C125708 (MONDO:equivalentTo)
DOID:0111086 (MONDO:equivalentTo)
EFO:0009046 (MONDO:equivalentTo)

Subsets

gard_rare, rare, nord_rare, clingen

exactMatch

http://purl.obolibrary.org/obo/DOID_0111086

http://purl.obolibrary.org/obo/NCIT_C125708

https://omim.org/entry/614082

has related synonym

Fanconi anemia, complementation group G

MONDO:0013565

seeAlso

https://search.clinicalgenome.org/kb/conditions/MONDO:0013565

Term relations

Subclass of:

Fanconi anemia