Shoulder girdle muscle atrophy

Symptom Information:

Symptom ID: HPO:0003724
Synonyms:
Shoulder girdle atrophy [HPO:0003724]
Shoulder girdle muscle wasting [HPO:0003724]
Shoulder-girdle muscle atrophy [HPO:0003724]
Shoulder girdle atrophy [OMIM:Shoulder girdle atrophy]
Shoulder girdle muscle atrophy [OMIM:Shoulder girdle muscle atrophy]
Shoulder-girdle muscle atrophy [OMIM:Shoulder-girdle muscle atrophy]
Quality:
Cross references:
OMIM: "Shoulder girdle atrophy" [OMIM:Shoulder girdle atrophy]
OMIM: "Shoulder girdle muscle atrophy" [OMIM:Shoulder girdle muscle atrophy]
OMIM: "Shoulder-girdle muscle atrophy" [OMIM:Shoulder-girdle muscle atrophy]
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)
                   Shoulder girdle muscle atrophy(HPO:0003724)
MedDRA:
Database Frequency: 14 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant Charcot-Marie-Tooth disease type 2C (Orphanet:99937)
Autosomal dominant Emery-Dreifuss muscular dystrophy (Orphanet:98853)
Autosomal dominant limb-girdle muscular dystrophy type 1H (Orphanet:238755)
Autosomal recessive Emery-Dreifuss muscular dystrophy (Orphanet:98855)
Autosomal recessive limb-girdle muscular dystrophy type 2E (Orphanet:119)
Autosomal recessive limb-girdle muscular dystrophy type 2H (Orphanet:1878)
Cap myopathy (Orphanet:171881)
Congenital muscular dystrophy with cerebellar involvement (Orphanet:370959)
Duchenne muscular dystrophy (Orphanet:98896)
Facioscapulohumeral dystrophy (Orphanet:269)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia (Orphanet:52430)
NEMALINE MYOPATHY 1 (OMIM:609284)
SCAPULOPERONEAL SYNDROME, NEUROGENIC, KAESER TYPE (OMIM:181400)
Scapuloperoneal amyotrophy (Orphanet:85146)