Online Mendelian Inheritance in Man - CRIGLER-NAJJAR SYNDROME, TYPE II - Classes

Preferred Name	CRIGLER-NAJJAR SYNDROME, TYPE II
Synonyms	HBLRCN2
ID	http://purl.bioontology.org/ontology/OMIM/606785
altLabel	HBLRCN2 HYPERBILIRUBINEMIA, CRIGLER-NAJJAR TYPE II
cui	C2931132
Gene Locus	2q37
Gene Symbol	UGT1A1 GNT1 BILIQTL1 UGT1
Has manifestation	http://purl.bioontology.org/ontology/OMIM/MTHU003834 http://purl.bioontology.org/ontology/OMIM/MTHU003837 http://purl.bioontology.org/ontology/OMIM/MTHU002997 http://purl.bioontology.org/ontology/OMIM/MTHU029556 http://purl.bioontology.org/ontology/OMIM/MTHU033556 http://purl.bioontology.org/ontology/OMIM/MTHU003833 http://purl.bioontology.org/ontology/OMIM/MTHU003836 http://purl.bioontology.org/ontology/OMIM/MTHU033557
MIMTYPEMEANING	Phenotype description, molecular basis known.
notation	606785
OMIM Entry Type	3
OMIM MimType Value	pound
prefLabel	CRIGLER-NAJJAR SYNDROME, TYPE II
tui	T047

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Delete	Mapping To	Ontology	Source
	http://purl.bioontology.org/ontology/MESH/C536213	Medical Subject Headings	CUI