Sensory impairment

Symptom Information:

Symptom ID: HPO:0003474
Synonyms:
Hypoaesthesia [HPO:0003474]
Hypoesthesia [HPO:0003474]
Hypoesthesia [Orphanet:43420]
Hypesthesia (finding) [Orphanet:43420]
Reduced sensation of skin (finding) [Orphanet:43420]
Sensory impairment [OMIM:Sensory impairment]
Paresthesia/dysesthesia/hypoesthesia/anesthesia/numbness [Orphanet:43420]
Hypoaesthesia [Orphanet:43420]
Hypoaesthesia [MedDRA:10020937]
Body numbness [MedDRA:10020937]
Hypalgesia [MedDRA:10020937]
Hypesthesia [MedDRA:10020937]
Hypoalgesia [MedDRA:10020937]
Hypoesthesia [MedDRA:10020937]
Hypoesthesia of gloves-socks type [MedDRA:10020937]
Localised numbness [MedDRA:10020937]
Numbness [MedDRA:10020937]
Numbness along 7th cranial nerve [MedDRA:10020937]
Numbness along L 7th cranial nerve [MedDRA:10020937]
Numbness facial [MedDRA:10020937]
Numbness generalized [MedDRA:10020937]
Numbness in back of head [MedDRA:10020937]
Numbness in face [MedDRA:10020937]
Numbness in fingers [MedDRA:10020937]
Numbness in hands, forearms, elbows [MedDRA:10020937]
Numbness in leg [MedDRA:10020937]
Numbness in shoulder [MedDRA:10020937]
Numbness localised [MedDRA:10020937]
Numbness localized [MedDRA:10020937]
Numbness of fingers [MedDRA:10020937]
Numbness of head [MedDRA:10020937]
Numbness of limbs [MedDRA:10020937]
Numbness of limbs-trunk [MedDRA:10020937]
Numbness of lower extremities [MedDRA:10020937]
Numbness of upper arm [MedDRA:10020937]
Numbness of upper extremities [MedDRA:10020937]
Scalp numbness [MedDRA:10020937]
Tactile sense reduced [MedDRA:10020937]
Numbness of extremities [MedDRA:10020937]
Numbness in hand [MedDRA:10020937]
Numbness in toes [MedDRA:10020937]
Numbness in feet [MedDRA:10020937]
Hypoaesthesia facial [MedDRA:10020937]
Hypaesthesia [MedDRA:10020937]
Numbness generalised [MedDRA:10020937]
Facial numbness [OMIM:Facial numbness]
Hypesthesia [OMIM:Hypesthesia]
Numbness [OMIM:Numbness]
Sensory impairment (in some patients) [OMIM:Sensory impairment (in some patients)]
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]
Graphoesthesia [IBIS,cm]
Quality:
Cross references:
Orphanet:43420 "Paresthesia/dysesthesia/hypoesthesia/anesthesia/numbness" [Orphanet:43420]
OMIM: "Sensory impairment" [OMIM:Sensory impairment]
OMIM: "Facial numbness" [OMIM:Facial numbness]
OMIM: "Hypesthesia" [OMIM:Hypesthesia]
OMIM: "Numbness" [OMIM:Numbness]
OMIM: "Sensory impairment (in some patients)" [OMIM:Sensory impairment (in some patients)]
OMIM: "Sensory loss" [OMIM:Sensory loss]
UMLS:C0392699 "Dysesthesia" [Orphanet:43420]
UMLS:C0278134 "Absence of sensation" [Orphanet:43420]
Is a (Direct Parents):
MedDRA Sensory abnormalities NEC
HPO         Peripheral neuropathy
Orphanet Paresthesia
Orphanet Sensitive trouble/deficit
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)
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)