Limb muscle weakness

Symptom Information:

Symptom ID: HPO:0003690
Synonyms:
Limb weakness [HPO:0003690]
Limb muscle weakness [OMIM:Limb muscle weakness]
Limb weakness [OMIM:Limb weakness]
Limb muscle weakness (distal greater than proximal) [OMIM:Limb muscle weakness (distal greater than proximal)]
Quality:
Cross references:
OMIM: "Limb muscle weakness" [OMIM:Limb muscle weakness]
OMIM: "Limb weakness" [OMIM:Limb weakness]
OMIM: "Limb muscle weakness (distal greater than proximal)" [OMIM:Limb muscle weakness (distal greater than proximal)]
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 muscle weakness(HPO:0003690)
MedDRA:
Database Frequency: 41 / 7739
Resource:

All diseases associated with this symptom:

Arnold-Chiari malformation type I (Orphanet:268882)
Arnold-Chiari malformation type II (Orphanet:1136)
Autosomal dominant Charcot-Marie-Tooth disease type 2O (Orphanet:284232)
Autosomal dominant progressive external ophthalmoplegia (Orphanet:254892)
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A (Orphanet:217055)
Autosomal recessive limb-girdle muscular dystrophy type 2B (Orphanet:268)
Autosomal recessive spastic paraplegia type 46 (Orphanet:320391)
CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS (OMIM:606842)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Charcot-Marie-Tooth disease type 4F (Orphanet:99952)
Choreoacanthocytosis (Orphanet:2388)
Corpus callosum agenesis - neuronopathy (Orphanet:1496)
Diaphyseal medullary stenosis - bone malignancy (Orphanet:85182)
Emery-Dreifuss muscular dystrophy (Orphanet:261)
Glycogen storage disease due to acid maltase deficiency, infantile onset (Orphanet:308552)
Hereditary motor and sensory neuropathy type 6 (Orphanet:90120)
Hurler-Scheie syndrome (Orphanet:93476)
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia (Orphanet:52430)
Kennedy disease (Orphanet:481)
MYASTHENIA GRAVIS (OMIM:254200)
MYASTHENIC SYNDROME, CONGENITAL, 4A, SLOW-CHANNEL (OMIM:605809)
Mitochondrial DNA depletion syndrome, myopathic form (Orphanet:254875)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
NEMALINE MYOPATHY 2 (OMIM:256030)
NEMALINE MYOPATHY 4 (OMIM:609285)
NEMALINE MYOPATHY 6 (OMIM:609273)
Nemaline myopathy (Orphanet:607)
OCULAR MYOPATHY WITH CURARE SENSITIVITY (OMIM:257600)
Oculopharyngeal muscular dystrophy (Orphanet:270)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 1 (OMIM:157640)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 3 (OMIM:609286)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 4 (OMIM:610131)
Primary CD59 deficiency (Orphanet:169464)
Primary basilar impression (Orphanet:2285)
REFSUM DISEASE, CLASSIC (OMIM:266500)
Refsum disease (Orphanet:773)
Spinal muscular atrophy with respiratory distress (Orphanet:98920)
Spinocerebellar ataxia type 18 (Orphanet:98771)
Spondyloepiphyseal dysplasia, Reardon type (Orphanet:163662)
Synaptic congenital myasthenic syndromes (Orphanet:98915)
Syringomyelia (Orphanet:3280)