Paresthesia
Symptom Information:
Symptom ID: | HPO:0003401 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Quality: | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Cross references: |
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Is a (Direct Parents): |
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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) Paresthesia(HPO:0003401) MedDRA: Nervous system disorders(MedDRA:10029205) Neurological disorders NEC(MedDRA:10029305) Paraesthesias and dysaesthesias(MedDRA:10033788) Paresthesia(HPO:0003401) |
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Database Frequency: | 42 / 7739 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ARTHRITIS, SACROILIAC | (OMIM:108100) |
ATTRV122I amyloidosis | (Orphanet:85451) |
Acute intermittent porphyria | (Orphanet:79276) |
Adrenomyeloneuropathy | (Orphanet:139399) |
Adult polyglucosan body disease | (Orphanet:206583) |
Arnold-Chiari malformation type I | (Orphanet:268882) |
Autosomal dominant spastic paraplegia type 3 | (Orphanet:100984) |
Autosomal dominant spastic paraplegia type 4 | (Orphanet:100985) |
BARTTER SYNDROME, ANTENATAL, TYPE 1 | (OMIM:601678) |
BARTTER SYNDROME, ANTENATAL, TYPE 2 | (OMIM:241200) |
Bartter syndrome | (Orphanet:112) |
Bartter syndrome with hypocalcemia | (Orphanet:263417) |
CREST syndrome | (Orphanet:90290) |
Cronkhite-Canada syndrome | (Orphanet:2930) |
EPILEPSY, NOCTURNAL FRONTAL LOBE, 4 | (OMIM:610353) |
Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
Fabry disease | (Orphanet:324) |
Familial paroxysmal ataxia | (Orphanet:97) |
Gitelman syndrome | (Orphanet:358) |
Gräsbeck-Imerslund disease | (Orphanet:35858) |
HYPOCALCEMIA, AUTOSOMAL DOMINANT 2 | (OMIM:615361) |
Hereditary arterial and articular multiple calcification syndrome | (Orphanet:289601) |
Hereditary thermosensitive neuropathy | (Orphanet:84093) |
Homocystinuria due to methylene tetrahydrofolate reductase deficiency | (Orphanet:395) |
INTRINSIC FACTOR DEFICIENCY | (OMIM:261000) |
MELAS | (Orphanet:550) |
MULTIPLE SCLEROSIS, SUSCEPTIBILITY TO | (OMIM:126200) |
MYXEDEMA | (OMIM:255900) |
McLeod neuroacanthocytosis syndrome | (Orphanet:59306) |
NEUROPATHY, HEREDITARY SENSORY, TYPE ID | (OMIM:613708) |
NEUROPATHY, PAINFUL | (OMIM:256870) |
Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity | (Orphanet:53583) |
Polyneuropathy - hand defect | (Orphanet:2926) |
Porphyria due to ALA dehydratase deficiency | (Orphanet:100924) |
Protein R deficiency | (Orphanet:2967) |
Proximal renal tubular acidosis | (Orphanet:47159) |
RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 1 | (OMIM:102300) |
Sneddon syndrome | (Orphanet:820) |
Syringomyelia | (Orphanet:3280) |
Wilson disease | (Orphanet:905) |
X-linked Charcot-Marie-Tooth disease type 1 | (Orphanet:101075) |
X-linked cerebral adrenoleukodystrophy | (Orphanet:139396) |