Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	FANCONI ANEMIA, COMPLEMENTATION GROUP V
Synonyms	FANCV
ID	http://purl.bioontology.org/ontology/OMIM/617243
altLabel	FANCV
cui	C4310652
Gene Locus	1p36
Gene Symbol	MAD2L2 FANCV MAD2B
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU001686 http://purl.bioontology.org/ontology/OMIM/MTHU004258 http://purl.bioontology.org/ontology/OMIM/MTHU002606 http://purl.bioontology.org/ontology/OMIM/MTHU056586 http://purl.bioontology.org/ontology/OMIM/MTHU056588 http://purl.bioontology.org/ontology/OMIM/MTHU056590 http://purl.bioontology.org/ontology/OMIM/MTHU001001 http://purl.bioontology.org/ontology/OMIM/MTHU000212 http://purl.bioontology.org/ontology/OMIM/MTHU000145 http://purl.bioontology.org/ontology/OMIM/MTHU056589 http://purl.bioontology.org/ontology/OMIM/MTHU056587 http://purl.bioontology.org/ontology/OMIM/MTHU036682 http://purl.bioontology.org/ontology/OMIM/MTHU036340 http://purl.bioontology.org/ontology/OMIM/MTHU018752
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	617243
OMIM Entry Type	3
OMIM MimType Value	pound
prefLabel	FANCONI ANEMIA, COMPLEMENTATION GROUP V
tui	T047

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Delete	Mapping To	Ontology	Source
	http://purl.obolibrary.org/obo/DOID_0111080	Human Disease Ontology 123	LOOM