Skip to
  1. Homepage
  2. Rare diseases
  3. Genes
Simple search

Simple search

*
(*) mandatory field




 

LAMA2 - laminin, alpha 2

Orpha number ORPHA122961
OMIM 156225
HGNC 6482
UniProtKB P24043
Genatlas LAMA2
Ensembl ENSG00000196569
IUPHAR-DB -
Reactome P24043
Synonym(s) congenital muscular dystrophy, Laminin, alpha 2 (merosin, congenital muscular dystrophy), LAMM, merosin

Diseases list



 Assessed
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.