MUSCULAR DYSTROPHY, HEMIZYGOUS LETHAL TYPE

General Information (adopted from Orphanet):

Synonyms, Signs:
Number of Symptoms 1
OrphanetNr:
OMIM Id: 309950
ICD-10:
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance:
Age of onset:

Disease classification (adopted from Orphanet):

Parent Diseases: No data available.

Symptom Information: Sort by abundance 

1
(HPO:0006785) Limb-girdle muscular dystrophy 14 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: