Distal muscle weakness
Symptom Information:
Symptom ID: | HPO:0002460 | |||||||||||||||||||
Synonyms: |
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Quality: | ||||||||||||||||||||
Cross references: |
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Is a (Direct Parents): |
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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) Distal muscle weakness(HPO:0002460) MedDRA: |
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Database Frequency: | 122 / 7739 | |||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AMYOTROPHIC LATERAL SCLEROSIS 5 | (OMIM:602099) |
AMYOTROPHIC LATERAL SCLEROSIS 8 | (OMIM:608627) |
AMYOTROPHIC LATERAL SCLEROSIS 9 | (OMIM:611895) |
AMYOTROPHIC LATERAL SCLEROSIS WITH POLYGLUCOSAN BODIES | (OMIM:205250) |
Alpha-N-acetylgalactosaminidase deficiency type 2 | (Orphanet:79280) |
Alpha-crystallinopathy | (Orphanet:98910) |
Amyotrophic lateral sclerosis type 4 | (Orphanet:357043) |
Autosomal dominant Charcot-Marie-Tooth disease type 2A1 | (Orphanet:99946) |
Autosomal dominant Charcot-Marie-Tooth disease type 2A2 | (Orphanet:99947) |
Autosomal dominant Charcot-Marie-Tooth disease type 2B | (Orphanet:99936) |
Autosomal dominant Charcot-Marie-Tooth disease type 2C | (Orphanet:99937) |
Autosomal dominant Charcot-Marie-Tooth disease type 2D | (Orphanet:99938) |
Autosomal dominant Charcot-Marie-Tooth disease type 2E | (Orphanet:99939) |
Autosomal dominant Charcot-Marie-Tooth disease type 2F | (Orphanet:99940) |
Autosomal dominant Charcot-Marie-Tooth disease type 2G | (Orphanet:99941) |
Autosomal dominant Charcot-Marie-Tooth disease type 2I | (Orphanet:99942) |
Autosomal dominant Charcot-Marie-Tooth disease type 2J | (Orphanet:99943) |
Autosomal dominant Charcot-Marie-Tooth disease type 2K | (Orphanet:99944) |
Autosomal dominant Charcot-Marie-Tooth disease type 2L | (Orphanet:99945) |
Autosomal dominant Charcot-Marie-Tooth disease type 2M | (Orphanet:228179) |
Autosomal dominant Charcot-Marie-Tooth disease type 2N | (Orphanet:228174) |
Autosomal dominant Charcot-Marie-Tooth disease type 2O | (Orphanet:284232) |
Autosomal dominant Charcot-Marie-Tooth disease type 2P | (Orphanet:300319) |
Autosomal dominant congenital benign spinal muscular atrophy | (Orphanet:1216) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type A | (Orphanet:100043) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B | (Orphanet:100044) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type C | (Orphanet:100045) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type D | (Orphanet:100046) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E | (Orphanet:93114) |
Autosomal dominant spastic paraplegia type 17 | (Orphanet:100998) |
Autosomal dominant spastic paraplegia type 38 | (Orphanet:171617) |
Autosomal dominant spastic paraplegia type 9 | (Orphanet:100990) |
Autosomal recessive Charcot-Marie-Tooth disease with hoarseness | (Orphanet:101097) |
Autosomal recessive centronuclear myopathy | (Orphanet:169186) |
Autosomal recessive intermediate Charcot-Marie-Tooth disease type C | (Orphanet:369867) |
Autosomal recessive limb-girdle muscular dystrophy type 2E | (Orphanet:119) |
Autosomal recessive limb-girdle muscular dystrophy type 2I | (Orphanet:34515) |
Autosomal recessive limb-girdle muscular dystrophy type 2J | (Orphanet:140922) |
Autosomal recessive lower motor neuron disease with childhood onset | (Orphanet:206580) |
Autosomal recessive progressive external ophthalmoplegia | (Orphanet:254886) |
Autosomal recessive spastic ataxia of Charlevoix-Saguenay | (Orphanet:98) |
Autosomal recessive spastic paraplegia type 48 | (Orphanet:306511) |
Bethlem myopathy | (Orphanet:610) |
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE | (OMIM:607706) |
CYSTINOSIS, NEPHROPATHIC | (OMIM:219800) |
Charcot-Marie-Tooth disease type 1A | (Orphanet:101081) |
Charcot-Marie-Tooth disease type 1B | (Orphanet:101082) |
Charcot-Marie-Tooth disease type 1C | (Orphanet:101083) |
Charcot-Marie-Tooth disease type 1D | (Orphanet:101084) |
Charcot-Marie-Tooth disease type 1E | (Orphanet:90658) |
Charcot-Marie-Tooth disease type 1F | (Orphanet:101085) |
Charcot-Marie-Tooth disease type 2B1 | (Orphanet:98856) |
Charcot-Marie-Tooth disease type 2B2 | (Orphanet:101101) |
Charcot-Marie-Tooth disease type 2H | (Orphanet:101102) |
Charcot-Marie-Tooth disease type 4A | (Orphanet:99948) |
Charcot-Marie-Tooth disease type 4B1 | (Orphanet:99955) |
Charcot-Marie-Tooth disease type 4B2 | (Orphanet:99956) |
Charcot-Marie-Tooth disease type 4C | (Orphanet:99949) |
Charcot-Marie-Tooth disease type 4D | (Orphanet:99950) |
Charcot-Marie-Tooth disease type 4E | (Orphanet:99951) |
Charcot-Marie-Tooth disease type 4G | (Orphanet:99953) |
Charcot-Marie-Tooth disease type 4J | (Orphanet:139515) |
Dejerine-Sottas syndrome | (Orphanet:64748) |
Desminopathy | (Orphanet:98909) |
Distal hereditary motor neuropathy type 1 | (Orphanet:139518) |
Distal hereditary motor neuropathy type 5 | (Orphanet:139536) |
Distal hereditary motor neuropathy type 7 | (Orphanet:139589) |
Distal hereditary motor neuropathy, Jerash type | (Orphanet:139552) |
Distal myopathy with anterior tibial onset | (Orphanet:178400) |
Distal myopathy with vocal cord weakness | (Orphanet:600) |
Distal myopathy, Welander type | (Orphanet:603) |
Distal spinal muscular atrophy type 3 | (Orphanet:139547) |
Duchenne muscular dystrophy | (Orphanet:98896) |
GIANT AXONAL NEUROPATHY 2, AUTOSOMAL DOMINANT | (OMIM:610100) |
Giant axonal neuropathy | (Orphanet:643) |
Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia | (Orphanet:79091) |
Hereditary motor and sensory neuropathy type 5 | (Orphanet:64751) |
Hereditary motor and sensory neuropathy type 6 | (Orphanet:90120) |
Hereditary sensory and autonomic neuropathy type 1 | (Orphanet:36386) |
Inclusion body myositis | (Orphanet:611) |
Laing distal myopathy | (Orphanet:59135) |
MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE) | (OMIM:603041) |
MIYOSHI MUSCULAR DYSTROPHY 3 | (OMIM:613319) |
MYOPATHY, DISTAL, 3 | (OMIM:610099) |
MYOPATHY, DISTAL, INFANTILE-ONSET | (OMIM:160300) |
Mitochondrial neurogastrointestinal encephalomyopathy | (Orphanet:298) |
Miyoshi myopathy | (Orphanet:45448) |
Myosclerosis | (Orphanet:289380) |
NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET | (OMIM:616263) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIC | (OMIM:613376) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VA | (OMIM:600794) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VB | (OMIM:614751) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIA | (OMIM:158580) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB | (OMIM:607641) |
NEUROPATHY, CONGENITAL, WITH ARTHROGRYPOSIS MULTIPLEX | (OMIM:162370) |
NEUROPATHY, HEREDITARY SENSORIMOTOR, WITH UPPER MOTOR NEURON, VISUALPATHWAY AND AUTONOMIC DISTURBANCE | (OMIM:162380) |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC | (OMIM:613640) |
NONAKA MYOPATHY | (OMIM:605820) |
Navajo neurohepatopathy | (Orphanet:255229) |
Neurodegeneration with brain iron accumulation due to C19orf12 mutation | (Orphanet:289560) |
Neurologic Waardenburg-Shah syndrome | (Orphanet:163746) |
OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE | (OMIM:258650) |
Oculopharyngeal muscular dystrophy | (Orphanet:270) |
Oculopharyngodistal myopathy | (Orphanet:98897) |
PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS | (OMIM:614369) |
POLYGLUCOSAN BODY MYOPATHY 2 | (OMIM:616199) |
Posterior column ataxia - retinitis pigmentosa | (Orphanet:88628) |
RADICULONEUROPATHY, FATAL NEONATAL | (OMIM:266250) |
Roussy-Lévy syndrome | (Orphanet:3115) |
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1 | (OMIM:606002) |
Spheroid body myopathy | (Orphanet:268129) |
Spinal muscular atrophy with respiratory distress | (Orphanet:98920) |
Spinocerebellar ataxia with axonal neuropathy type 2 | (Orphanet:64753) |
Steinert myotonic dystrophy | (Orphanet:273) |
Trichomegaly - retina pigmentary degeneration - dwarfism | (Orphanet:3363) |
VACUOLAR NEUROMYOPATHY | (OMIM:601846) |
X-linked Charcot-Marie-Tooth disease type 1 | (Orphanet:101075) |
X-linked Charcot-Marie-Tooth disease type 2 | (Orphanet:101076) |
X-linked Charcot-Marie-Tooth disease type 3 | (Orphanet:101077) |
X-linked Charcot-Marie-Tooth disease type 5 | (Orphanet:99014) |
X-linked distal spinal muscular atrophy | (Orphanet:139557) |
X-linked intellectual disability due to GRIA3 anomalies | (Orphanet:364028) |