Log In|Sign Up
ENLama2-Related Muscular Dystrophy
Alias:
Muscular Dystrophy Congenital, Merosin Negative
Laminin Alpha-2 Deficient Muscular Dystrophy
Muscular Dystrophy Due to Lama2 Deficiency
Merosin-Deficient Muscular Dystrophy
Laminin Alpha 2 Deficiency
Lama2 Md
Mdc1a
Favorite
Lama2-Related Muscular Dystrophy, also known as muscular dystrophy congenital, merosin negative, is related to muscular dystrophy, congenital merosin-deficient, 1a and muscular dystrophy, limb-girdle, autosomal recessive 23. An important gene associated with Lama2-Related Muscular Dystrophy is LAMA2 (Laminin Subunit Alpha 2). Affiliated tissues include tongue and lung.
Related ID：
Basic Information
Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
Medical Symptom
#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
Gene & Mutation
#
Gene
Function
Score
Mutations
Related Drugs
Name
CAS Number
Status
Phase
Disease Model
Category
Name
MGI
Related Gene
Strain of Origin
Publications
References Literature
Title
PMID
Journal
Year
IF
