Limb-girdle muscular dystrophy

Symptom Information:

Symptom ID: HPO:0006785
Synonyms:
Limb-girdle muscular dystrophy [OMIM:Limb-girdle muscular dystrophy]
Muscular dystrophy, limb-girdle [OMIM:Muscular dystrophy, limb-girdle]
Quality:
Cross references:
OMIM: "Limb-girdle muscular dystrophy" [OMIM:Limb-girdle muscular dystrophy]
OMIM: "Muscular dystrophy, limb-girdle" [OMIM:Muscular dystrophy, limb-girdle]
Is a (Direct Parents):
HPO         Limb-girdle 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)
                   Limb-girdle muscular dystrophy(HPO:0006785)
MedDRA:
Database Frequency: 14 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant limb-girdle muscular dystrophy type 1G (Orphanet:55596)
Autosomal recessive limb-girdle muscular dystrophy type 2C (Orphanet:353)
Autosomal recessive limb-girdle muscular dystrophy type 2D (Orphanet:62)
Autosomal recessive limb-girdle muscular dystrophy type 2E (Orphanet:119)
Autosomal recessive limb-girdle muscular dystrophy type 2F (Orphanet:219)
Autosomal recessive limb-girdle muscular dystrophy type 2G (Orphanet:34514)
Autosomal recessive limb-girdle muscular dystrophy type 2M (Orphanet:206554)
Autosomal recessive limb-girdle muscular dystrophy type 2Q (Orphanet:254361)
Autosomal recessive limb-girdle muscular dystrophy type 2S (Orphanet:369840)
Emery-Dreifuss muscular dystrophy (Orphanet:261)
Glycogen storage disease due to acid maltase deficiency, late-onset (Orphanet:420429)
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUTFRONTOTEMPORAL DEMENTIA 3 (OMIM:615424)
MUSCULAR DYSTROPHY, HEMIZYGOUS LETHAL TYPE (OMIM:309950)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 7 (OMIM:616052)