Sensory impairment
Symptom Information:
Symptom ID: | HPO:0003474 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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) MedDRA: Nervous system disorders(MedDRA:10029205) Neurological disorders NEC(MedDRA:10029305) Sensory abnormalities NEC(MedDRA:10040021) Sensory impairment(HPO:0003474) |
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Database Frequency: | 54 / 7739 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ALACRIMA, ACHALASIA, AND MENTAL RETARDATION SYNDROME | (OMIM:615510) |
Adrenomyeloneuropathy | (Orphanet:139399) |
Adult polyglucosan body disease | (Orphanet:206583) |
Alpha-N-acetylgalactosaminidase deficiency type 1 | (Orphanet:79279) |
Arachnoiditis | (Orphanet:137817) |
Arnold-Chiari malformation type I | (Orphanet:268882) |
Ataxia with vitamin E deficiency | (Orphanet:96) |
Autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures | (Orphanet:209341) |
Autosomal recessive spastic paraplegia type 48 | (Orphanet:306511) |
Autosomal recessive spastic paraplegia type 7 | (Orphanet:99013) |
Buerger disease | (Orphanet:36258) |
CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE | (OMIM:118230) |
CHILD syndrome | (Orphanet:139) |
Camurati-Engelmann disease | (Orphanet:1328) |
Citrullinemia type II | (Orphanet:247585) |
Cobb syndrome | (Orphanet:53721) |
Complete androgen insensitivity syndrome | (Orphanet:99429) |
Deafness - enamel hypoplasia - nail defects | (Orphanet:3220) |
Ehlers-Danlos syndrome due to tenascin-X deficiency | (Orphanet:230839) |
Friedreich ataxia 1 | (OMIM:229300) |
Granulomatosis with polyangiitis | (Orphanet:900) |
Gräsbeck-Imerslund disease | (Orphanet:35858) |
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type | (Orphanet:324703) |
Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
IMMUNODEFICIENCY 23 | (OMIM:615816) |
INTRINSIC FACTOR DEFICIENCY | (OMIM:261000) |
Isolated spina bifida | (Orphanet:823) |
Juvenile amyotrophic lateral sclerosis | (Orphanet:300605) |
Juvenile primary lateral sclerosis | (Orphanet:247604) |
Krabbe disease | (Orphanet:487) |
Leber plus disease | (Orphanet:99718) |
MELAS | (Orphanet:550) |
MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO | (OMIM:126200) |
Multiple sclerosis - ichthyosis - factor VIII deficiency | (Orphanet:3151) |
NEUROPATHY, PAINFUL | (OMIM:256870) |
Navajo neurohepatopathy | (Orphanet:255229) |
Necrotizing encephalomyelopathy, subacute, of Leigh, adult | (OMIM:161700) |
Neurofibromatosis type 2 | (Orphanet:637) |
Neurogenic thoracic outlet syndrome | (Orphanet:100073) |
Perrault Syndrome 5 | (OMIM:616138) |
Polyneuropathy - hand defect | (Orphanet:2926) |
REFSUM DISEASE, CLASSIC | (OMIM:266500) |
Refsum disease | (Orphanet:773) |
Sneddon syndrome | (Orphanet:820) |
Spastic paraplegia type 2 | (Orphanet:99015) |
Syringomyelia | (Orphanet:3280) |
Thoracic outlet syndrome | (Orphanet:97330) |
Von Hippel-Lindau disease | (Orphanet:892) |
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 cerebral adrenoleukodystrophy | (Orphanet:139396) |