Distal amyotrophy
Symptom Information:
Symptom ID: | HPO:0003693 | ||||||||||||||||||||
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 morphology(HPO:0011805) Skeletal muscle atrophy(HPO:0003202) Distal amyotrophy(HPO:0003693) MedDRA: |
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Database Frequency: | 118 / 7739 | ||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE | (OMIM:205100) |
AMYOTROPHIC LATERAL SCLEROSIS 5 | (OMIM:602099) |
AMYOTROPHIC LATERAL SCLEROSIS 9 | (OMIM:611895) |
AMYOTROPHIC LATERAL SCLEROSIS, JUVENILE, WITH DEMENTIA | (OMIM:205200) |
Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency | (Orphanet:329314) |
Ataxia - hypogonadism - choroidal dystrophy | (Orphanet:1180) |
Ataxia - oculomotor apraxia type 1 | (Orphanet:1168) |
Ataxia-telangiectasia-like disorder | (Orphanet:251347) |
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 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 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 spastic paraplegia type 17 | (Orphanet:100998) |
Autosomal dominant spastic paraplegia type 3 | (Orphanet:100984) |
Autosomal dominant spastic paraplegia type 38 | (Orphanet:171617) |
Autosomal recessive Charcot-Marie-Tooth disease with hoarseness | (Orphanet:101097) |
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A | (Orphanet:217055) |
Autosomal recessive lower motor neuron disease with childhood onset | (Orphanet:206580) |
Autosomal recessive spastic ataxia of Charlevoix-Saguenay | (Orphanet:98) |
Autosomal recessive spastic paraplegia type 11 | (Orphanet:2822) |
Autosomal recessive spastic paraplegia type 15 | (Orphanet:100996) |
Autosomal recessive spastic paraplegia type 20 | (Orphanet:101000) |
Autosomal recessive spastic paraplegia type 26 | (Orphanet:101006) |
Autosomal recessive spastic paraplegia type 39 | (Orphanet:139480) |
Autosomal recessive spastic paraplegia type 43 | (Orphanet:320370) |
CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM | (OMIM:118301) |
CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE | (OMIM:118230) |
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) |
Dejerine-Sottas syndrome | (Orphanet:64748) |
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, Nonaka type | (Orphanet:602) |
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) |
Glycogen storage disease due to glycogen debranching enzyme deficiency | (Orphanet:366) |
Hereditary motor and sensory neuropathy type 5 | (Orphanet:64751) |
Hereditary motor and sensory neuropathy type 6 | (Orphanet:90120) |
Hereditary sensory and autonomic neuropathy with spastic paraplegia | (Orphanet:139578) |
INCLUSION BODY MYOPATHY 2, AUTOSOMAL RECESSIVE | (OMIM:600737) |
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUTFRONTOTEMPORAL DEMENTIA 1 | (OMIM:167320) |
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia | (Orphanet:52430) |
Intellectual deficit - cataracts - calcified pinnae - myopathy | (Orphanet:3042) |
Intellectual deficit, X-linked, Miles-Carpenter type | (Orphanet:85283) |
Intellectual disability-developmental delay-contractures syndrome | (Orphanet:3454) |
Juvenile amyotrophic lateral sclerosis | (Orphanet:300605) |
LARYNGEAL ABDUCTOR PARALYSIS WITH CEREBELLAR ATAXIA AND MOTOR NEUROPATHY | (OMIM:606183) |
MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE) | (OMIM:603041) |
MYASTHENIC SYNDROME, CONGENITAL, 10 | (OMIM:254300) |
MYOPATHY, DISTAL, 3 | (OMIM:610099) |
Mitochondrial neurogastrointestinal encephalomyopathy | (Orphanet:298) |
Miyoshi myopathy | (Orphanet:45448) |
Myotilin-related myofibrillar myopathy without spheroid body | (Orphanet:98911) |
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6 | (OMIM:615643) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VB | (OMIM:614751) |
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, TYPE ID | (OMIM:613708) |
NONAKA MYOPATHY | (OMIM:605820) |
Neurodegeneration with brain iron accumulation due to C19orf12 mutation | (Orphanet:289560) |
Neurologic Waardenburg-Shah syndrome | (Orphanet:163746) |
Oculopharyngodistal myopathy | (Orphanet:98897) |
PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS | (OMIM:614369) |
PEROXISOME BIOGENESIS DISORDER 6B | (OMIM:614871) |
Perrault Syndrome 5 | (OMIM:616138) |
Polyneuropathy - hearing loss - ataxia - retinitis pigmentosa - cataract | (Orphanet:171848) |
Postsynaptic congenital myasthenic syndromes | (Orphanet:98913) |
Roussy-Lévy syndrome | (Orphanet:3115) |
SPASTIC ATAXIA 2, AUTOSOMAL RECESSIVE | (OMIM:611302) |
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1 | (OMIM:606002) |
Spastic paraplegia - neuropathy - poikiloderma | (Orphanet:2821) |
Spastic paraplegia-optic atrophy-neuropathy syndrome | (Orphanet:320406) |
Spinal muscular atrophy with respiratory distress | (Orphanet:98920) |
Spinocerebellar ataxia type 1 | (Orphanet:98755) |
Spinocerebellar ataxia type 1 with axonal neuropathy | (Orphanet:94124) |
Spinocerebellar ataxia type 2 | (Orphanet:98756) |
Spinocerebellar ataxia type 3 | (Orphanet:98757) |
Spinocerebellar ataxia with axonal neuropathy type 2 | (Orphanet:64753) |
Tangier disease | (Orphanet:31150) |
Trichomegaly - retina pigmentary degeneration - dwarfism | (Orphanet:3363) |
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) |