Limb-girdle muscle atrophy

Symptom Information:

Symptom ID: HPO:0003797
Synonyms:
Limb-girdle myopathy [HPO:0003797]
Limb-girdle muscle atrophy [OMIM:Limb-girdle muscle atrophy]
Quality:
Cross references:
OMIM: "Limb-girdle muscle atrophy" [OMIM:Limb-girdle muscle atrophy]
Is a (Direct Parents):
HPO         Skeletal muscle atrophy
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle morphology(HPO:0011805)
             Skeletal muscle atrophy(HPO:0003202)
                Limb-girdle muscle atrophy(HPO:0003797)
MedDRA:
Database Frequency: 8 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive Emery-Dreifuss muscular dystrophy (Orphanet:98855)
Autosomal recessive limb girdle muscular dystrophy type 2A (Orphanet:267)
Autosomal recessive limb-girdle muscular dystrophy type 2D (Orphanet:62)
Becker muscular dystrophy (Orphanet:98895)
Distal myopathy, Nonaka type (Orphanet:602)
Glycogen storage disease due to acid maltase deficiency, late-onset (Orphanet:420429)
INCLUSION BODY MYOPATHY 2, AUTOSOMAL RECESSIVE (OMIM:600737)
MYOPATHY WITH GIANT ABNORMAL MITOCHONDRIA (OMIM:255140)