Medical Subject Headings

Last uploaded: November 5, 2019
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Preferred Name

Cardiomyopathy, Familial Hypertrophic, 6
ID

http://purl.bioontology.org/ontology/MESH/C563436
cui

C1833236
HM

D024741
Inverse of RB

0
Mapped to

http://purl.bioontology.org/ontology/MESH/D024741
MDA

20121105
MeSH Frequency

0
notation

C563436
prefLabel

Cardiomyopathy, Familial Hypertrophic, 6
SC

3
Scope Statement

mutation in PRKAG2
TERMUI

T802904
TH

OMIM (2013)
tui

T047
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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/602743 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/600858 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/600858 Online Mendelian Inheritance in Man LOOM