Preferred Name

RENIN

Synonyms

RENAL TUBULAR DYSGENESIS

ID

http://purl.bioontology.org/ontology/OMIM/179820

altLabel

RENAL TUBULAR DYSGENESIS

HYPERPRORENINEMIA, FAMILIAL

TUBULOINTERSTITIAL KIDNEY DISEASE, AUTOSOMAL DOMINANT, 4

REN

cui

C1419338

C0266313

C4016362

C2751310

Gene Locus

1q32

Gene Symbol

ADTKD4

REN

RTD

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

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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/MESH/C567760 Medical Subject Headings / 医学主题词表 CUI
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C113591 National Cancer Institute Thesaurus / 美国国家癌症研究所词典 LOOM
http://purl.obolibrary.org/obo/PR_000013883 Protein Ontology / 蛋白质本体 LOOM
http://purl.obolibrary.org/obo/PR_000013883 中国人类表型本体 / Human Phenotype Ontology China LOOM
http://purl.obolibrary.org/obo/PR_000013883 Uber Anatomy Ontology / 超级解剖学本体 LOOM
http://purl.obolibrary.org/obo/PR_000013883 Cell Ontology / 细胞本体 LOOM
http://purl.bmicc.cn/ontology/ICD10CN/Q61.4 《国际疾病分类》第10版中文版 / International Classification of Diseases, 10th Edition, China CUI
http://purl.bioontology.org/ontology/LNC/LP32149-4 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 LOOM
http://purl.bioontology.org/ontology/MESH/D012083 Medical Subject Headings / 医学主题词表 LOOM
http://purl.bioontology.org/ontology/MESH/C537048 Medical Subject Headings / 医学主题词表 CUI
http://purl.bioontology.org/ontology/LNC/LP15273-3 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 LOOM
http://purl.bioontology.org/ontology/LNC/MTHU003186 Logical Observation Identifier Names and Codes / 逻辑观察标识符名称和代码 LOOM
http://www.orpha.net/ORDO/Orphanet_138530 Orphanet Rare Disease Ontology / Orphanet罕见病本体 LOOM