Sensory neuropathy

Symptom Information:

Symptom ID: HPO:0000763
Synonyms:
Peripheral sensory neuropathy [HPO:0000763]
Peripheral sensory neuropathy [OMIM:Peripheral sensory neuropathy]
Sensory neuropathy [OMIM:Sensory neuropathy]
Peripheral neuropathy, sensory [OMIM:Peripheral neuropathy, sensory]
Sensory neuropathy (not a prominent feature) [OMIM:Sensory neuropathy (not a prominent feature)]
Peripheral sensory neuropathy [MedDRA:10034620]
Quality:
Cross references:
OMIM: "Peripheral sensory neuropathy" [OMIM:Peripheral sensory neuropathy]
OMIM: "Sensory neuropathy" [OMIM:Sensory neuropathy]
OMIM: "Peripheral neuropathy, sensory" [OMIM:Peripheral neuropathy, sensory]
OMIM: "Sensory neuropathy (not a prominent feature)" [OMIM:Sensory neuropathy (not a prominent feature)]
Is a (Direct Parents):
HPO         Peripheral neuropathy
MedDRA Peripheral neuropathies NEC
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)
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)