Medical Subject Headings

Last uploaded: November 5, 2019

Preferred Name	Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency
ID	http://purl.bioontology.org/ontology/MESH/C564317
cui	C1842898
Has mapping qualifier	http://purl.bioontology.org/ontology/MESH/Q000151
HM	D009136/Q000151
Inverse of RB	0
Mapped to	http://purl.bioontology.org/ontology/MESH/D009136
MDA	20121105
MeSH Frequency	0
MMR	20131106
notation	C564317
prefLabel	Muscular Dystrophy, Congenital, due to Partial LAMA2 Deficiency
SC	3
Scope Statement	mutation in laminin alpha-2 (LAMA2)
TERMUI	T829440
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/156225	Online Mendelian Inheritance in Man	CUI
	http://purl.bioontology.org/ontology/OMIM/607855	Online Mendelian Inheritance in Man	CUI