Distal sensory impairment

Symptom Information:

Symptom ID: HPO:0002936
Synonyms:
Decreased distal sensation [HPO:0002936]
Distal sensation loss [HPO:0002936]
Distal sensory impairment in lower limbs [HPO:0002936]
Distal sensory impairment of the lower extremities [HPO:0002936]
Distal sensory loss [HPO:0002936]
Distal sensory loss, upper and lower limbs [HPO:0002936]
Loss of distal sensation [HPO:0002936]
Decreased distal sensation [OMIM:Decreased distal sensation]
Distal sensation loss [OMIM:Distal sensation loss]
Distal sensory impairment [OMIM:Distal sensory impairment]
Distal sensory impairment in lower limbs [OMIM:Distal sensory impairment in lower limbs]
Distal sensory impairment of the lower extremities [OMIM:Distal sensory impairment of the lower extremities]
Distal sensory loss [OMIM:Distal sensory loss]
Distal sensory loss, upper and lower limbs [OMIM:Distal sensory loss, upper and lower limbs]
Loss of distal sensation [OMIM:Loss of distal sensation]
Decreased distal sensation (in 1 of 3 patients) [OMIM:Decreased distal sensation (in 1 of 3 patients)]
Decreased distal sensation (less common) [OMIM:Decreased distal sensation (less common)]
Distal sensory impairment (20-50%) [OMIM:Distal sensory impairment (20-50%)]
Distal sensory impairment (in some patients) [OMIM:Distal sensory impairment (in some patients)]
Distal sensory impairment (lower limbs more affected than upper limbs) [OMIM:Distal sensory impairment (lower limbs more affected than upper limbs)]
Distal sensory loss (all modalities) [OMIM:Distal sensory loss (all modalities)]
Distal sensory loss (predominantly in lower limbs) [OMIM:Distal sensory loss (predominantly in lower limbs)]
Quality:
Cross references:
OMIM: "Decreased distal sensation" [OMIM:Decreased distal sensation]
OMIM: "Distal sensation loss" [OMIM:Distal sensation loss]
OMIM: "Distal sensory impairment" [OMIM:Distal sensory impairment]
OMIM: "Distal sensory impairment in lower limbs" [OMIM:Distal sensory impairment in lower limbs]
OMIM: "Distal sensory impairment of the lower extremities" [OMIM:Distal sensory impairment of the lower extremities]
OMIM: "Distal sensory loss" [OMIM:Distal sensory loss]
OMIM: "Distal sensory loss, upper and lower limbs" [OMIM:Distal sensory loss, upper and lower limbs]
OMIM: "Loss of distal sensation" [OMIM:Loss of distal sensation]
OMIM: "Decreased distal sensation (in 1 of 3 patients)" [OMIM:Decreased distal sensation (in 1 of 3 patients)]
OMIM: "Decreased distal sensation (less common)" [OMIM:Decreased distal sensation (less common)]
OMIM: "Distal sensory impairment (20-50%)" [OMIM:Distal sensory impairment (20-50%)]
OMIM: "Distal sensory impairment (in some patients)" [OMIM:Distal sensory impairment (in some patients)]
OMIM: "Distal sensory impairment (lower limbs more affected than upper limbs)" [OMIM:Distal sensory impairment (lower limbs more affected than upper limbs)]
OMIM: "Distal sensory loss (all modalities)" [OMIM:Distal sensory loss (all modalities)]
OMIM: "Distal sensory loss (predominantly in lower limbs)" [OMIM:Distal sensory loss (predominantly in lower limbs)]
Is a (Direct Parents):
HPO         Sensory impairment
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)
                      Distal sensory impairment(HPO:0002936)
MedDRA:
Database Frequency: 96 / 7739
Resource:

All diseases associated with this symptom:

ATAXIA-OCULOMOTOR APRAXIA 3 (OMIM:615217)
Adult polyglucosan body disease (Orphanet:206583)
Alpha-N-acetylgalactosaminidase deficiency type 2 (Orphanet:79280)
Ataxia - oculomotor apraxia type 1 (Orphanet:1168)
Autosomal dominant Charcot-Marie-Tooth disease type 2A1 (Orphanet:99946)
Autosomal dominant Charcot-Marie-Tooth disease type 2A2 (Orphanet:99947)
Autosomal dominant Charcot-Marie-Tooth disease type 2C (Orphanet:99937)
Autosomal dominant Charcot-Marie-Tooth disease type 2D (Orphanet:99938)
Autosomal dominant Charcot-Marie-Tooth disease type 2E (Orphanet:99939)
Autosomal dominant Charcot-Marie-Tooth disease type 2F (Orphanet:99940)
Autosomal dominant Charcot-Marie-Tooth disease type 2G (Orphanet:99941)
Autosomal dominant Charcot-Marie-Tooth disease type 2I (Orphanet:99942)
Autosomal dominant Charcot-Marie-Tooth disease type 2J (Orphanet:99943)
Autosomal dominant Charcot-Marie-Tooth disease type 2K (Orphanet:99944)
Autosomal dominant Charcot-Marie-Tooth disease type 2L (Orphanet:99945)
Autosomal dominant Charcot-Marie-Tooth disease type 2M (Orphanet:228179)
Autosomal dominant Charcot-Marie-Tooth disease type 2N (Orphanet:228174)
Autosomal dominant Charcot-Marie-Tooth disease type 2O (Orphanet:284232)
Autosomal dominant Charcot-Marie-Tooth disease type 2P (Orphanet:300319)
Autosomal dominant intermediate Charcot-Marie-Tooth disease type A (Orphanet:100043)
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B (Orphanet:100044)
Autosomal dominant intermediate Charcot-Marie-Tooth disease type C (Orphanet:100045)
Autosomal dominant intermediate Charcot-Marie-Tooth disease type D (Orphanet:100046)
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E (Orphanet:93114)
Autosomal dominant intermediate Charcot-Marie-Tooth disease type F (Orphanet:352670)
Autosomal dominant spastic paraplegia type 10 (Orphanet:100991)
Autosomal dominant spastic paraplegia type 31 (Orphanet:101011)
Autosomal recessive Charcot-Marie-Tooth disease with hoarseness (Orphanet:101097)
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A (Orphanet:217055)
Autosomal recessive intermediate Charcot-Marie-Tooth disease type B (Orphanet:254334)
Autosomal recessive intermediate Charcot-Marie-Tooth disease type C (Orphanet:369867)
Autosomal recessive spastic ataxia of Charlevoix-Saguenay (Orphanet:98)
Autosomal recessive spastic paraplegia type 28 (Orphanet:101008)
Autosomal recessive spastic paraplegia type 43 (Orphanet:320370)
Autosomal recessive spastic paraplegia type 44 (Orphanet:320401)
Autosomal recessive spastic paraplegia type 55 (Orphanet:320375)
CARDIONEUROMYOPATHY WITH HYALINE MASSES AND NEMALINE RODS (OMIM:606842)
CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURALHEARING LOSS, AND SKELETAL DYSPLASIA (OMIM:616007)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2S (OMIM:616155)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2T (OMIM:616233)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2U (OMIM:616280)
CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE D (OMIM:616039)
CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY AND FRIEDREICH ATAXIA,COMBINED (OMIM:302900)
Cataract - ataxia - deafness (Orphanet:1368)
Charcot-Marie-Tooth disease type 1A (Orphanet:101081)
Charcot-Marie-Tooth disease type 1B (Orphanet:101082)
Charcot-Marie-Tooth disease type 1C (Orphanet:101083)
Charcot-Marie-Tooth disease type 1E (Orphanet:90658)
Charcot-Marie-Tooth disease type 1F (Orphanet:101085)
Charcot-Marie-Tooth disease type 2B1 (Orphanet:98856)
Charcot-Marie-Tooth disease type 2B2 (Orphanet:101101)
Charcot-Marie-Tooth disease type 2H (Orphanet:101102)
Charcot-Marie-Tooth disease type 4A (Orphanet:99948)
Charcot-Marie-Tooth disease type 4B1 (Orphanet:99955)
Charcot-Marie-Tooth disease type 4B2 (Orphanet:99956)
Charcot-Marie-Tooth disease type 4B3 (Orphanet:363981)
Charcot-Marie-Tooth disease type 4C (Orphanet:99949)
Charcot-Marie-Tooth disease type 4D (Orphanet:99950)
Charcot-Marie-Tooth disease type 4F (Orphanet:99952)
Charcot-Marie-Tooth disease type 4H (Orphanet:99954)
Charcot-Marie-Tooth disease type 4J (Orphanet:139515)
Combined oxidative phosphorylation defect type 7 (Orphanet:254930)
Dejerine-Sottas syndrome (Orphanet:64748)
Distal myopathy with vocal cord weakness (Orphanet:600)
Familial encephalopathy with neuroserpin inclusion bodies (Orphanet:85110)
Giant axonal neuropathy (Orphanet:643)
HYPERTROPHIC NEUROPATHY AND CATARACT (OMIM:239900)
Hereditary motor and sensory neuropathy type 5 (Orphanet:64751)
Hereditary motor and sensory neuropathy type 6 (Orphanet:90120)
Hereditary motor and sensory neuropathy, Okinawa type (Orphanet:90117)
Hereditary sensory and autonomic neuropathy type 1 (Orphanet:36386)
Hereditary sensory and autonomic neuropathy type 1B (Orphanet:139564)
Hereditary sensory and autonomic neuropathy with spastic paraplegia (Orphanet:139578)
Kufor-Rakeb syndrome (Orphanet:306674)
MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE) (OMIM:603041)
Mitochondrial neurogastrointestinal encephalomyopathy (Orphanet:298)
Muscular dystrophy, Selcen type (Orphanet:199340)
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, ADULT-ONSET, WITH ANOSMIA (OMIM:608720)
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC (OMIM:613640)
NEUROPATHY, HEREDITARY SENSORY, TYPE ID (OMIM:613708)
Neurologic Waardenburg-Shah syndrome (Orphanet:163746)
OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE (OMIM:258650)
PARTIAL LIPODYSTROPHY, CONGENITAL CATARACTS, AND NEURODEGENERATIONSYNDROME (OMIM:606721)
PEROXISOME BIOGENESIS DISORDER 6B (OMIM:614871)
Parkinsonim due to ATP13A2 deficiency (Orphanet:314632)
Polyneuropathy - hearing loss - ataxia - retinitis pigmentosa - cataract (Orphanet:171848)
Roussy-Lévy syndrome (Orphanet:3115)
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY (OMIM:181405)
Spinocerebellar ataxia type 4 (Orphanet:98765)
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 distal spinal muscular atrophy (Orphanet:139557)
X-linked hereditary sensory and autonomic neuropathy with deafness (Orphanet:139583)