Medical Subject Headings

Last uploaded: November 5, 2019
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Preferred Name

Peroxisome Biogenesis Disorder, Complementation Group 1
ID

http://purl.bioontology.org/ontology/MESH/C566568
cui

C1865803
HM

D018901
Inverse of RB

0
Mapped to

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

20121105
MeSH Frequency

1
notation

C566568
prefLabel

Peroxisome Biogenesis Disorder, Complementation Group 1
SC

3
TERMUI

T808750
TH

OMIM (2013)
tui

T047
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Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/OMIM/214100 Online Mendelian Inheritance in Man CUI