Paresthesia

Symptom Information:

Symptom ID: HPO:0003401
Synonyms:
Paresthesias [HPO:0003401]
Numbness (finding) [Orphanet:43420]
Has tingling sensation (finding) [Orphanet:43420]
Paresthesia (finding) [Orphanet:43420]
Tactile hypesthesia (finding) [Orphanet:43420]
paresthesia [HPO:0003401]
Numbness [Orphanet:43420]
Paresthesia [Orphanet:43420]
Has tingling sensation [Orphanet:43420]
Hypesthesia [Orphanet:43420]
Paresthesia [OMIM:Paresthesia]
Paresthesias [OMIM:Paresthesias]
Paresthesia/dysesthesia/hypoesthesia/anesthesia/numbness [Orphanet:43420]
Paraesthesia [Orphanet:43420]
Tingling sensation [Orphanet:43420]
Paraesthesia [MedDRA:10033775]
Abnormal touch sensation [MedDRA:10033775]
Acroparaesthesia [MedDRA:10033775]
Disturbance of skin sensation [MedDRA:10033775]
Drawing neck [MedDRA:10033775]
Electric shock sensation [MedDRA:10033775]
Facial paraesthesia [MedDRA:10033775]
Paraesthesia distal [MedDRA:10033775]
Paraesthesia generalised [MedDRA:10033775]
Paraesthesia NEC [MedDRA:10033775]
Paraesthesia of fingers [MedDRA:10033775]
Paraesthesia of limbs [MedDRA:10033775]
Paraesthesia skin [MedDRA:10033775]
Parasthesia [MedDRA:10033775]
Parasthesiae distal [MedDRA:10033775]
Parasthesiae skin [MedDRA:10033775]
Paresthesia [MedDRA:10033775]
Paresthesia distal [MedDRA:10033775]
Paresthesia skin [MedDRA:10033775]
Pins and needles [MedDRA:10033775]
Pricking skin sensation [MedDRA:10033775]
Prickling of hand [MedDRA:10033775]
Tingling [MedDRA:10033775]
Tingling feet/hands [MedDRA:10033775]
Tingling sensation [MedDRA:10033775]
Tingling skin [MedDRA:10033775]
Paraesthesia of scalp [MedDRA:10033775]
Paraesthesia hand [MedDRA:10033775]
Paraesthesia foot [MedDRA:10033775]
Paraesthesia upper limb [MedDRA:10033775]
Paraesthesia lower limb [MedDRA:10033775]
Paraesthesia ear [MedDRA:10033775]
Paresthesia ear [MedDRA:10033775]
Paresthesia foot [MedDRA:10033775]
Paresthesia generalized [MedDRA:10033775]
Paresthesia hand [MedDRA:10033775]
Paresthesia lower limb [MedDRA:10033775]
Paresthesia of fingers [MedDRA:10033775]
Paresthesia of limbs [MedDRA:10033775]
Paresthesia of scalp [MedDRA:10033775]
Paresthesia upper limb [MedDRA:10033775]
Facial paresthesia [MedDRA:10033775]
Acroparesthesia [MedDRA:10033775]
Tingling of extremity [MedDRA:10033775]
Localized tingling [MedDRA:10033775]
Localised tingling [MedDRA:10033775]
Paraesthesia aggravated [MedDRA:10033775]
Paresthesia aggravated [MedDRA:10033775]
Ascending paraesthesia [MedDRA:10033775]
Ascending paresthesia [MedDRA:10033775]
Hypesthesia [OMIM:Hypesthesia]
Numbness [OMIM:Numbness]
Tingling (in some patients) [OMIM:Tingling (in some patients)]
Tingling sensation [OMIM:Tingling sensation]
Dysaesthesia [MedDRA:10013886]
Dysesthesia [Orphanet:43420]
Dysesthesia (finding) [Orphanet:43420]
Sensory loss [MedDRA:10040030]
Anesthesia [Orphanet:43420]
Absence of sensation (finding) [Orphanet:43420]
Absence of sensation [Orphanet:43420]
Sensory loss [OMIM:Sensory loss]
Quality:
Cross references:
Orphanet:43420 "Paresthesia/dysesthesia/hypoesthesia/anesthesia/numbness" [Orphanet:43420]
OMIM: "Paresthesia" [OMIM:Paresthesia]
OMIM: "Paresthesias" [OMIM:Paresthesias]
OMIM: "Hypesthesia" [OMIM:Hypesthesia]
OMIM: "Numbness" [OMIM:Numbness]
OMIM: "Tingling (in some patients)" [OMIM:Tingling (in some patients)]
OMIM: "Tingling sensation" [OMIM:Tingling sensation]
OMIM: "Sensory loss" [OMIM:Sensory loss]
UMLS:C2242996 "paresthesia" [HPO:0003401]
UMLS:C0028643 "Numbness" [Orphanet:43420]
UMLS:C0030554 "Paresthesia" [Orphanet:43420]
UMLS:C2242996 "Has tingling sensation" [Orphanet:43420]
UMLS:C0020580 "Hypesthesia" [Orphanet:43420]
UMLS:C0392699 "Dysesthesia" [Orphanet:43420]
UMLS:C0278134 "Absence of sensation" [Orphanet:43420]
Is a (Direct Parents):
Orphanet Sensitive trouble/deficit
MedDRA Paraesthesias and dysaesthesias
HPO         Sensory neuropathy
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)