Preferred Label : merosin;
UMLS semantic type : T116 - Amino Acid, Peptide, or Protein; T123 - Biologically Active Substance;
Is substance : O;
Origin ID : M0012197;
UMLS CUI : C0376333;
Automatic exact mappings (from CISMeF team)
Related record
Semantic type(s)
https://www.afm-telethon.fr/fr/fiches-maladies/dystrophie-musculaire-congenitale-avec-deficit-primaire-en-merosine
2020
France
popular works
principal
congenital dystrophy, nos
congenital muscular dysdrophy
laminin
muscular dystrophy congenital, merosin negative
Muscular dystrophy
muscular dystrophies
merosin
muscular dystrophy, nos
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