Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019

Preferred Name	RENIN
Synonyms	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 2
ID	http://purl.bioontology.org/ontology/OMIM/179820
altLabel	HYPERURICEMIC NEPHROPATHY, FAMILIAL JUVENILE, 2 RENAL TUBULAR DYSGENESIS HYPERPRORENINEMIA, FAMILIAL REN
cui	C1419338 C0266313 C4016362 C2751310
Gene Locus	1q32
Gene Symbol	HNFJ2 REN
Has allelic variant	http://purl.bioontology.org/ontology/OMIM/179820.0001 http://purl.bioontology.org/ontology/OMIM/179820.0005 http://purl.bioontology.org/ontology/OMIM/179820.0006 http://purl.bioontology.org/ontology/OMIM/179820.0007 http://purl.bioontology.org/ontology/OMIM/179820.0002 http://purl.bioontology.org/ontology/OMIM/179820.0003 http://purl.bioontology.org/ontology/OMIM/179820.0004
MIMTYPEMEANING	Gene with known sequence
notation	179820
OMIM Entry Type	1
OMIM MimType Value	star
prefLabel	RENIN
tui	T028 T033 T047

Delete	Subject	Author	Type	Created
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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/MESH/C567760	Medical Subject Headings	CUI
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C113591	National Cancer Institute Thesaurus	LOOM
http://purl.obolibrary.org/obo/PR_000013883	Human Phenotype Ontology China	LOOM
http://purl.obolibrary.org/obo/PR_000013883	International Classification of Diseases Ontology	LOOM
http://purl.obolibrary.org/obo/PR_000013883	Protein Ontology	LOOM
http://purl.bmicc.cn/ontology/ICD10CN/Q61.4	International Classification of Diseases, 10th Edition, China	CUI
http://purl.bioontology.org/ontology/LNC/LP32149-4	Logical Observation Identifier Names and Codes	LOOM
http://purl.bioontology.org/ontology/MESH/D012083	Medical Subject Headings	LOOM
http://purl.bioontology.org/ontology/MESH/C537048	Medical Subject Headings	CUI
http://purl.bioontology.org/ontology/LNC/LP15273-3	Logical Observation Identifier Names and Codes	LOOM
http://purl.bioontology.org/ontology/LNC/MTHU003186	Logical Observation Identifier Names and Codes	LOOM