Sensory neuropathy
Symptom Information:
Symptom ID: | HPO:0000763 | ||||||
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 nervous system(HPO:0000707) Abnormality of nervous system morphology(HPO:0012639) Abnormal peripheral nervous system morphology(HPO:0000759) Peripheral neuropathy(HPO:0009830) Sensory neuropathy(HPO:0000763) MedDRA: Nervous system disorders(MedDRA:10029205) Peripheral axonal neuropathy(HPO:0003477) Peripheral neuropathies NEC(MedDRA:10034607) Sensory neuropathy(HPO:0000763) |
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Database Frequency: | 78 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
46,XY complete gonadal dysgenesis | (Orphanet:242) |
Acromegaly | (Orphanet:963) |
Acute intermittent porphyria | (Orphanet:79276) |
Adiposis dolorosa | (Orphanet:36397) |
Alpha-N-acetylgalactosaminidase deficiency type 1 | (Orphanet:79279) |
Alveolar echinococcosis | (Orphanet:284) |
Arachnoiditis | (Orphanet:137817) |
Autosomal dominant hypocalcemia | (Orphanet:428) |
Autosomal dominant spastic paraplegia type 9 | (Orphanet:100990) |
Autosomal recessive spastic paraplegia type 11 | (Orphanet:2822) |
Autosomal recessive spastic paraplegia type 48 | (Orphanet:306511) |
Behçet disease | (Orphanet:117) |
Benign familial infantile seizures | (Orphanet:306) |
Beta-thalassemia major | (Orphanet:231214) |
Buerger disease | (Orphanet:36258) |
CEREBELLAR ATAXIA, NEUROPATHY, AND VESTIBULAR AREFLEXIA SYNDROME | (OMIM:614575) |
CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM | (OMIM:118301) |
Cervical hypertrichosis - peripheral neuropathy | (Orphanet:2218) |
Choreoacanthocytosis | (Orphanet:2388) |
Chédiak-Higashi syndrome | (Orphanet:167) |
Cogan syndrome | (Orphanet:1467) |
Congenital hypothyroidism | (Orphanet:442) |
Congenital ichthyosis - microcephalus - tetraplegia | (Orphanet:2271) |
Corpus callosum agenesis - neuronopathy | (Orphanet:1496) |
Cronkhite-Canada syndrome | (Orphanet:2930) |
Ehlers-Danlos syndrome, hypermobility type | (Orphanet:285) |
Eosinophilic fasciitis | (Orphanet:3165) |
Essential thrombocythemia | (Orphanet:3318) |
Fabry disease | (Orphanet:324) |
Familial symmetric lipomatosis | (Orphanet:2398) |
Familial thrombocytosis | (Orphanet:71493) |
Fragile X-associated tremor/ataxia syndrome | (Orphanet:93256) |
Friedreich ataxia 1 | (OMIM:229300) |
Giant cell arteritis | (Orphanet:397) |
Granulomatosis with polyangiitis | (Orphanet:900) |
Haim-Munk syndrome | (Orphanet:2342) |
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type | (Orphanet:324703) |
Hereditary motor and sensory neuropathy type 5 | (Orphanet:64751) |
Hereditary neuropathy with liability to pressure palsies | (Orphanet:640) |
Hereditary sensory and autonomic neuropathy type 6 | (Orphanet:314381) |
Hyperkalemic periodic paralysis | (Orphanet:682) |
Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
Kearns-Sayre syndrome | (Orphanet:480) |
Kennedy disease | (Orphanet:481) |
Ledderhose disease | (Orphanet:199251) |
Lyme disease | (Orphanet:91546) |
MERRF | (Orphanet:551) |
Malignant atrophic papulosis | (Orphanet:679) |
McLeod neuroacanthocytosis syndrome | (Orphanet:59306) |
Microscopic polyangiitis | (Orphanet:727) |
Mucopolysaccharidosis type 1 | (Orphanet:579) |
Multiple endocrine neoplasia type 2 | (Orphanet:653) |
Myotonia fluctuans | (Orphanet:99734) |
NARP syndrome | (Orphanet:644) |
NEUROPATHY, HEREDITARY SENSORY, ATYPICAL | (OMIM:256860) |
NEUROPATHY, HEREDITARY SENSORY, TYPE IE | (OMIM:614116) |
NEUROPATHY, HEREDITARY SENSORY, X-LINKED | (OMIM:310470) |
Neuralgic amyotrophy | (Orphanet:2901) |
Neurofibromatosis type 1 | (Orphanet:636) |
Neurogenic thoracic outlet syndrome | (Orphanet:100073) |
Non-polyposis Turcot syndrome | (Orphanet:99817) |
Palmoplantar keratoderma-spastic paralysis syndrome | (Orphanet:2201) |
Phakomatosis pigmentovascularis | (Orphanet:2875) |
Polyarteritis nodosa | (Orphanet:767) |
Porphyria | (Orphanet:738) |
Pseudoachondroplasia | (Orphanet:750) |
Rabies | (Orphanet:770) |
SPASTIC PARAPLEGIA 61, AUTOSOMAL RECESSIVE | (OMIM:615685) |
Spinocerebellar ataxia type 18 | (Orphanet:98771) |
Spinocerebellar ataxia type 25 | (Orphanet:101111) |
Spinocerebellar ataxia type 4 | (Orphanet:98765) |
Spinocerebellar ataxia type 6 | (Orphanet:98758) |
Spinocerebellar ataxia type 8 | (Orphanet:98760) |
Stüve-Wiedemann syndrome | (Orphanet:3206) |
TRAPS syndrome | (Orphanet:32960) |
Thoracic outlet syndrome | (Orphanet:97330) |
X-linked Charcot-Marie-Tooth disease type 1 | (Orphanet:101075) |
X-linked Charcot-Marie-Tooth disease type 4 | (Orphanet:101078) |