Online Mendelian Inheritance in Man - MYELOPEROXIDASE DEFICIENCY - Classes | NCBO OntoPortal Appliance

Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

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Preferred Name	MYELOPEROXIDASE DEFICIENCY
Synonyms	MPO DEFICIENCY
ID	http://purl.bioontology.org/ontology/OMIM/254600
altLabel	MPO DEFICIENCY MPOD
cui	C0398595
Gene Locus	17q23.1
Gene Symbol	MPO
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU010943 http://purl.bioontology.org/ontology/OMIM/MTHU010947 http://purl.bioontology.org/ontology/OMIM/MTHU028349 http://purl.bioontology.org/ontology/OMIM/MTHU037777 http://purl.bioontology.org/ontology/OMIM/MTHU010946 http://purl.bioontology.org/ontology/OMIM/MTHU010944 http://purl.bioontology.org/ontology/OMIM/MTHU010942
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	254600
OMIM Entry Type	3
OMIM MimType Value	pound
prefLabel	MYELOPEROXIDASE DEFICIENCY
tui	T047

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Delete	Mapping To	Ontology	Source
	http://purl.bioontology.org/ontology/MESH/C562864	Medical Subject Headings	CUI
	http://purl.bioontology.org/ontology/MESH/C562864	Medical Subject Headings	LOOM