Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	FACTOR VII DEFICIENCY
Synonyms	HYPOPROCONVERTINEMIA
ID	http://purl.bioontology.org/ontology/OMIM/227500
altLabel	HYPOPROCONVERTINEMIA F7 DEFICIENCY
cui	C0015503
Gene Locus	13q34
Gene Symbol	F7
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU036809 http://purl.bioontology.org/ontology/OMIM/MTHU007302 http://purl.bioontology.org/ontology/OMIM/MTHU000759 http://purl.bioontology.org/ontology/OMIM/MTHU032016 http://purl.bioontology.org/ontology/OMIM/MTHU009110 http://purl.bioontology.org/ontology/OMIM/MTHU012705 http://purl.bioontology.org/ontology/OMIM/MTHU027990 http://purl.bioontology.org/ontology/OMIM/MTHU041887 http://purl.bioontology.org/ontology/OMIM/MTHU013061 http://purl.bioontology.org/ontology/OMIM/MTHU032017
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	227500
OMIM Entry Type	3
OMIM MimType Value	pound
prefLabel	FACTOR VII DEFICIENCY
tui	T047

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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/MESH/D005168	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/MESH/D005168	Medical Subject Headings	LOOM
http://purl.bioontology.org/ontology/ICD10CM/D68.2	International Classification of Diseases, Version 10 - Clinical Modification	CUI
http://purl.obolibrary.org/obo/DOID_2215	Human Disease Ontology 123	LOOM