Medical Subject Headings

Last uploaded: November 5, 2019
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Preferred Name

Hyperinsulinemic Hypoglycemia, Familial, 5
ID

http://purl.bioontology.org/ontology/MESH/C566494
cui

C1864952
HM

D006946

D007003
Inverse of RB

0
Mapped to

http://purl.bioontology.org/ontology/MESH/D007003

http://purl.bioontology.org/ontology/MESH/D006946
MDA

20121105
MeSH Frequency

0
notation

C566494
prefLabel

Hyperinsulinemic Hypoglycemia, Familial, 5
SC

3
Scope Statement

mutation in insulin receptor
TERMUI

T808618
TH

OMIM (2013)
tui

T047
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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/609968 Online Mendelian Inheritance in Man CUI
http://purl.bioontology.org/ontology/OMIM/609968 Online Mendelian Inheritance in Man LOOM
http://purl.bioontology.org/ontology/OMIM/147670 Online Mendelian Inheritance in Man CUI