Distal amyotrophy

Symptom Information:

Symptom ID: HPO:0003693
Synonyms:
Amyotrophy of distal limb muscles [HPO:0003693]
Distal amyotrophy, especially of the hands and feet [HPO:0003693]
Distal limb muscle atrophy [HPO:0003693]
Distal muscle atrophy [HPO:0003693]
Distal muscle atrophy, upper and lower limbs [HPO:0003693]
Distal muscle wasting [HPO:0003693]
Distal muscular atrophy [HPO:0003693]
Muscle atrophy, distal [HPO:0003693]
Amyotrophy of distal limb muscles [OMIM:Amyotrophy of distal limb muscles]
Distal amyotrophy [OMIM:Distal amyotrophy]
Distal amyotrophy, especially of the hands and feet [OMIM:Distal amyotrophy, especially of the hands and feet]
Distal limb muscle atrophy [OMIM:Distal limb muscle atrophy]
Distal muscle atrophy [OMIM:Distal muscle atrophy]
Distal muscle atrophy, upper and lower limbs [OMIM:Distal muscle atrophy, upper and lower limbs]
Distal muscle wasting [OMIM:Distal muscle wasting]
Distal muscular atrophy [OMIM:Distal muscular atrophy]
Muscle atrophy, distal [OMIM:Muscle atrophy, distal]
Distal amyotrophy (hands and feet) [OMIM:Distal amyotrophy (hands and feet)]
Distal limb muscle atrophy (less common) [OMIM:Distal limb muscle atrophy (less common)]
Distal muscle atrophy (lower limbs more affected than upper limbs) [OMIM:Distal muscle atrophy (lower limbs more affected than upper limbs)]
Quality:
Cross references:
OMIM: "Amyotrophy of distal limb muscles" [OMIM:Amyotrophy of distal limb muscles]
OMIM: "Distal amyotrophy" [OMIM:Distal amyotrophy]
OMIM: "Distal amyotrophy, especially of the hands and feet" [OMIM:Distal amyotrophy, especially of the hands and feet]
OMIM: "Distal limb muscle atrophy" [OMIM:Distal limb muscle atrophy]
OMIM: "Distal muscle atrophy" [OMIM:Distal muscle atrophy]
OMIM: "Distal muscle atrophy, upper and lower limbs" [OMIM:Distal muscle atrophy, upper and lower limbs]
OMIM: "Distal muscle wasting" [OMIM:Distal muscle wasting]
OMIM: "Distal muscular atrophy" [OMIM:Distal muscular atrophy]
OMIM: "Muscle atrophy, distal" [OMIM:Muscle atrophy, distal]
OMIM: "Distal amyotrophy (hands and feet)" [OMIM:Distal amyotrophy (hands and feet)]
OMIM: "Distal limb muscle atrophy (less common)" [OMIM:Distal limb muscle atrophy (less common)]
OMIM: "Distal muscle atrophy (lower limbs more affected than upper limbs)" [OMIM:Distal muscle atrophy (lower limbs more affected than upper limbs)]
Is a (Direct Parents):
HPO         Skeletal 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)
                Distal amyotrophy(HPO:0003693)
MedDRA:
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)