Medical Subject Headings

Last uploaded: November 5, 2019

Preferred Name	Peroxisome Biogenesis Disorder, Complementation Group E
ID	http://purl.bioontology.org/ontology/MESH/C566569
cui	C1865804
HM	D018901
Inverse of RB	0
Mapped to	http://purl.bioontology.org/ontology/MESH/D018901
MDA	20121105
MeSH Frequency	0
notation	C566569
prefLabel	Peroxisome Biogenesis Disorder, Complementation Group E
SC	3
TERMUI	T808751
TH	OMIM (2013)
tui	T047

Delete	Subject	Author	Type	Created
No notes to display

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