Online Mendelian Inheritance in Man - HYPERBILIRUBINEMIA, ROTOR TYPE - Classes | NCBO OntoPortal Appliance

Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

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Preferred Name	HYPERBILIRUBINEMIA, ROTOR TYPE
Synonyms	ROTOR SYNDROME
ID	http://purl.bioontology.org/ontology/OMIM/237450
altLabel	ROTOR SYNDROME HBLRR
cui	C0220991
Gene Locus	12p12.2
Gene Symbol	OATP8 SLC21A8 SLCO1B3 HBLRR OATP1B3
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU032112 http://purl.bioontology.org/ontology/OMIM/MTHU002997 http://purl.bioontology.org/ontology/OMIM/MTHU032110 http://purl.bioontology.org/ontology/OMIM/MTHU032109 http://purl.bioontology.org/ontology/OMIM/MTHU032111 http://purl.bioontology.org/ontology/OMIM/MTHU000011 http://purl.bioontology.org/ontology/OMIM/MTHU032108
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	237450
OMIM Entry Type	3
OMIM MimType Value	pound
prefLabel	HYPERBILIRUBINEMIA, ROTOR TYPE
tui	T047

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Delete	Mapping To	Ontology	Source
	http://purl.bioontology.org/ontology/MESH/D006933	Medical Subject Headings	CUI
	http://purl.bioontology.org/ontology/ICD10CM/E80.6	International Classification of Diseases, Version 10 - Clinical Modification	CUI