Limb-girdle muscle weakness

Symptom Information:

Symptom ID: HPO:0003325
Synonyms:
Limb girdle weakness [HPO:0003325]
Muscle weakness, limb-girdle [HPO:0003325]
Muscular weakness, limb-girdle [HPO:0003325]
Limb girdle weakness [OMIM:Limb girdle weakness]
Limb-girdle muscle weakness [OMIM:Limb-girdle muscle weakness]
Muscle weakness, limb-girdle [OMIM:Muscle weakness, limb-girdle]
Muscular weakness, limb-girdle [OMIM:Muscular weakness, limb-girdle]
Limb-girdle muscle weakness (2 families) [OMIM:Limb-girdle muscle weakness (2 families)]
Quality:
Cross references:
OMIM: "Limb girdle weakness" [OMIM:Limb girdle weakness]
OMIM: "Limb-girdle muscle weakness" [OMIM:Limb-girdle muscle weakness]
OMIM: "Muscle weakness, limb-girdle" [OMIM:Muscle weakness, limb-girdle]
OMIM: "Muscular weakness, limb-girdle" [OMIM:Muscular weakness, limb-girdle]
OMIM: "Limb-girdle muscle weakness (2 families)" [OMIM:Limb-girdle muscle weakness (2 families)]
Is a (Direct Parents):
HPO         Muscle weakness
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the musculature(HPO:0003011)
          Abnormality of muscle physiology(HPO:0011804)
             Muscle weakness(HPO:0001324)
                Limb-girdle muscle weakness(HPO:0003325)
MedDRA:
Database Frequency: 22 / 7739
Resource:

All diseases associated with this symptom:

Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency (Orphanet:329314)
Alpha-crystallinopathy (Orphanet:98910)
Autosomal dominant limb-girdle muscular dystrophy type 1B (Orphanet:264)
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)
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 2K (Orphanet:86812)
Autosomal recessive limb-girdle muscular dystrophy type 2P (Orphanet:280333)
Becker muscular dystrophy (Orphanet:98895)
Bethlem myopathy (Orphanet:610)
Congenital muscular dystrophy type 1B (Orphanet:98893)
Diaphyseal medullary stenosis - bone malignancy (Orphanet:85182)
Distal myopathy, Nonaka type (Orphanet:602)
Duchenne muscular dystrophy (Orphanet:98896)
Emery-Dreifuss muscular dystrophy (Orphanet:261)
Glycogen storage disease due to acid maltase deficiency, late-onset (Orphanet:420429)
INCLUSION BODY MYOPATHY 2, AUTOSOMAL RECESSIVE (OMIM:600737)
MYASTHENIC SYNDROME, CONGENITAL, 14 (OMIM:616228)
Mitochondrial DNA deletion syndrome with progressive myopathy (Orphanet:352470)
X-linked Emery-Dreifuss muscular dystrophy (Orphanet:98863)