Medical Subject Headings

Last uploaded: November 5, 2019
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Preferred Name

Peroxisome Biogenesis Disorder, Complementation Group R
ID

http://purl.bioontology.org/ontology/MESH/C566635
cui

C1866352
HM

D018901
Inverse of RB

0
Mapped to

http://purl.bioontology.org/ontology/MESH/D018901
MDA

20121105
MeSH Frequency

0
notation

C566635
prefLabel

Peroxisome Biogenesis Disorder, Complementation Group R
SC

3
TERMUI

T808886
TH

OMIM (2013)
tui

T047
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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/614879 Online Mendelian Inheritance in Man CUI