Distal sensory impairment
Symptom Information:
Symptom ID: | HPO:0002936 | ||||||||||||||||||||||
Synonyms: |
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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 nervous system(HPO:0000707) Abnormality of nervous system morphology(HPO:0012639) Abnormal peripheral nervous system morphology(HPO:0000759) Peripheral neuropathy(HPO:0009830) Sensory impairment(HPO:0003474) Distal sensory impairment(HPO:0002936) MedDRA: |
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Database Frequency: | 96 / 7739 | ||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ATAXIA-OCULOMOTOR APRAXIA 3 | (OMIM:615217) |
Adult polyglucosan body disease | (Orphanet:206583) |
Alpha-N-acetylgalactosaminidase deficiency type 2 | (Orphanet:79280) |
Ataxia - oculomotor apraxia type 1 | (Orphanet:1168) |
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 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 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 intermediate Charcot-Marie-Tooth disease type F | (Orphanet:352670) |
Autosomal dominant spastic paraplegia type 10 | (Orphanet:100991) |
Autosomal dominant spastic paraplegia type 31 | (Orphanet:101011) |
Autosomal recessive Charcot-Marie-Tooth disease with hoarseness | (Orphanet:101097) |
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A | (Orphanet:217055) |
Autosomal recessive intermediate Charcot-Marie-Tooth disease type B | (Orphanet:254334) |
Autosomal recessive intermediate Charcot-Marie-Tooth disease type C | (Orphanet:369867) |
Autosomal recessive spastic ataxia of Charlevoix-Saguenay | (Orphanet:98) |
Autosomal recessive spastic paraplegia type 28 | (Orphanet:101008) |
Autosomal recessive spastic paraplegia type 43 | (Orphanet:320370) |
Autosomal recessive spastic paraplegia type 44 | (Orphanet:320401) |
Autosomal recessive spastic paraplegia type 55 | (Orphanet:320375) |
CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS | (OMIM:606842) |
CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURALHEARING LOSS, AND SKELETAL DYSPLASIA | (OMIM:616007) |
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S | (OMIM:616155) |
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2T | (OMIM:616233) |
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2U | (OMIM:616280) |
CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE D | (OMIM:616039) |
CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED | (OMIM:302900) |
Cataract - ataxia - deafness | (Orphanet:1368) |
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 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 4B3 | (Orphanet:363981) |
Charcot-Marie-Tooth disease type 4C | (Orphanet:99949) |
Charcot-Marie-Tooth disease type 4D | (Orphanet:99950) |
Charcot-Marie-Tooth disease type 4F | (Orphanet:99952) |
Charcot-Marie-Tooth disease type 4H | (Orphanet:99954) |
Charcot-Marie-Tooth disease type 4J | (Orphanet:139515) |
Combined oxidative phosphorylation defect type 7 | (Orphanet:254930) |
Dejerine-Sottas syndrome | (Orphanet:64748) |
Distal myopathy with vocal cord weakness | (Orphanet:600) |
Familial encephalopathy with neuroserpin inclusion bodies | (Orphanet:85110) |
Giant axonal neuropathy | (Orphanet:643) |
HYPERTROPHIC NEUROPATHY AND CATARACT | (OMIM:239900) |
Hereditary motor and sensory neuropathy type 5 | (Orphanet:64751) |
Hereditary motor and sensory neuropathy type 6 | (Orphanet:90120) |
Hereditary motor and sensory neuropathy, Okinawa type | (Orphanet:90117) |
Hereditary sensory and autonomic neuropathy type 1 | (Orphanet:36386) |
Hereditary sensory and autonomic neuropathy type 1B | (Orphanet:139564) |
Hereditary sensory and autonomic neuropathy with spastic paraplegia | (Orphanet:139578) |
Kufor-Rakeb syndrome | (Orphanet:306674) |
MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE) | (OMIM:603041) |
Mitochondrial neurogastrointestinal encephalomyopathy | (Orphanet:298) |
Muscular dystrophy, Selcen type | (Orphanet:199340) |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, ADULT-ONSET, WITH ANOSMIA | (OMIM:608720) |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC | (OMIM:613640) |
NEUROPATHY, HEREDITARY SENSORY, TYPE ID | (OMIM:613708) |
Neurologic Waardenburg-Shah syndrome | (Orphanet:163746) |
OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE | (OMIM:258650) |
PARTIAL LIPODYSTROPHY, CONGENITAL CATARACTS, AND NEURODEGENERATIONSYNDROME | (OMIM:606721) |
PEROXISOME BIOGENESIS DISORDER 6B | (OMIM:614871) |
Parkinsonim due to ATP13A2 deficiency | (Orphanet:314632) |
Polyneuropathy - hearing loss - ataxia - retinitis pigmentosa - cataract | (Orphanet:171848) |
Roussy-Lévy syndrome | (Orphanet:3115) |
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY | (OMIM:181405) |
Spinocerebellar ataxia type 4 | (Orphanet:98765) |
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 4 | (Orphanet:101078) |
X-linked Charcot-Marie-Tooth disease type 5 | (Orphanet:99014) |
X-linked distal spinal muscular atrophy | (Orphanet:139557) |
X-linked hereditary sensory and autonomic neuropathy with deafness | (Orphanet:139583) |