Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	FANCONI ANEMIA, COMPLEMENTATION GROUP R
Synonyms	FANCR
ID	http://purl.bioontology.org/ontology/OMIM/617244
altLabel	FANCR
cui	C4284093
Gene Locus	15q15.1
Gene Symbol	RECA MRMV2 RAD51A FANCR
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU038662 http://purl.bioontology.org/ontology/OMIM/MTHU000166 http://purl.bioontology.org/ontology/OMIM/MTHU056590 http://purl.bioontology.org/ontology/OMIM/MTHU035437 http://purl.bioontology.org/ontology/OMIM/MTHU056594 http://purl.bioontology.org/ontology/OMIM/MTHU056592 http://purl.bioontology.org/ontology/OMIM/MTHU034182 http://purl.bioontology.org/ontology/OMIM/MTHU001944 http://purl.bioontology.org/ontology/OMIM/MTHU003335 http://purl.bioontology.org/ontology/OMIM/MTHU057613 http://purl.bioontology.org/ontology/OMIM/MTHU056587 http://purl.bioontology.org/ontology/OMIM/MTHU056595 http://purl.bioontology.org/ontology/OMIM/MTHU036340 http://purl.bioontology.org/ontology/OMIM/MTHU056593 http://purl.bioontology.org/ontology/OMIM/MTHU056591 http://purl.bioontology.org/ontology/OMIM/MTHU002499 http://purl.bioontology.org/ontology/OMIM/MTHU001447
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	617244
OMIM Entry Type	3
OMIM MimType Value	pound
prefLabel	FANCONI ANEMIA, COMPLEMENTATION GROUP R
tui	T047

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Delete	Mapping To	Ontology	Source
	http://purl.obolibrary.org/obo/DOID_0111090	Human Disease Ontology 123	LOOM