Medical Subject Headings

Last uploaded: November 5, 2019
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Preferred Name

Hypertensive Nephropathy
ID

http://purl.bioontology.org/ontology/MESH/C563161
cui

C0848548
HM

D006977

D009393
Inverse of RB

0
Mapped to

http://purl.bioontology.org/ontology/MESH/D006977

http://purl.bioontology.org/ontology/MESH/D009393
MDA

20121105
MeSH Frequency

118
MMR

20150818
notation

C563161
prefLabel

Hypertensive Nephropathy
SC

3
Scope Statement

A hereditary disorder reported in an AFRICAN AMERICAN family. Nearly half of those affected had CHRONIC KIDNEY FAILURE and HYPERTENSION. PROTEINURIA and focal segmental glomerular sclerosis-like lesions (OMIM: 603278) with ARTERIOLE thickening were observed in one patient. Has been mapped to chromosome 9. OMIM: 608026
TERMUI

T802320
TH

OMIM (2013)
tui

T047
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Delete Mapping To Ontology Source
http://purl.bmicc.cn/ontology/ICD10CN/I12 International Classification of Diseases, 10th Edition, China CUI
http://purl.bioontology.org/ontology/OMIM/608026 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/608026 Online Mendelian Inheritance in Man LOOM
http://purl.bioontology.org/ontology/ICD10CM/I12 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C4757 National Cancer Institute Thesaurus LOOM
http://purl.bioontology.org/ontology/ICD10CM/I12.9 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/ICD10/I12 International Classification of Diseases, Version 10 CUI