Sensorimotor neuropathy

Symptom Information:

Symptom ID: HPO:0007141
Synonyms:
Mixed polyneuropathy [HPO:0007141]
Sensorimotor peripheral neuropathy [HPO:0007141]
Sensorimotor neuropathy [OMIM:Sensorimotor neuropathy]
Sensorimotor peripheral neuropathy [OMIM:Sensorimotor peripheral neuropathy]
Peripheral sensorimotor neuropathy [OMIM:Peripheral sensorimotor neuropathy]
Sensorimotor neuropathy (1 patient) [OMIM:Sensorimotor neuropathy (1 patient)]
Sensorimotor peripheral neuropathy (in some) [OMIM:Sensorimotor peripheral neuropathy (in some)]
Peripheral sensorimotor neuropathy [MedDRA:10056673]
Quality:
Cross references:
OMIM: "Sensorimotor neuropathy" [OMIM:Sensorimotor neuropathy]
OMIM: "Sensorimotor peripheral neuropathy" [OMIM:Sensorimotor peripheral neuropathy]
OMIM: "Peripheral sensorimotor neuropathy" [OMIM:Peripheral sensorimotor neuropathy]
OMIM: "Sensorimotor neuropathy (1 patient)" [OMIM:Sensorimotor neuropathy (1 patient)]
OMIM: "Sensorimotor peripheral neuropathy (in some)" [OMIM:Sensorimotor peripheral neuropathy (in some)]
Is a (Direct Parents):
MedDRA Peripheral neuropathies NEC
HPO         Peripheral 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)
                   Sensorimotor neuropathy(HPO:0007141)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Peripheral axonal neuropathy(HPO:0003477)
       Peripheral neuropathies NEC(MedDRA:10034607)
          Sensorimotor neuropathy(HPO:0007141)
Database Frequency: 27 / 7739
Resource:

All diseases associated with this symptom:

AL amyloidosis (Orphanet:85443)
ALPHA-METHYLACYL-CoA RACEMASE DEFICIENCY (OMIM:614307)
Autosomal dominant spastic paraplegia type 3 (Orphanet:100984)
Autosomal recessive spastic paraplegia type 11 (Orphanet:2822)
CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURALHEARING LOSS, AND SKELETAL DYSPLASIA (OMIM:616007)
COLD-INDUCED SWEATING SYNDROME 2 (OMIM:610313)
CREST syndrome (Orphanet:90290)
Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome (Orphanet:309854)
Early-onset spastic ataxia-neuropathy syndrome (Orphanet:313772)
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 (Orphanet:168566)
KRABBE DISEASE (OMIM:245200)
Krabbe disease (Orphanet:487)
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (Orphanet:5)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
NARP syndrome (Orphanet:644)
NEUROPATHY, HEREDITARY SENSORIMOTOR, WITH UPPER MOTOR NEURON, VISUALPATHWAY AND AUTONOMIC DISTURBANCE (OMIM:162380)
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC (OMIM:613640)
Navajo neurohepatopathy (Orphanet:255229)
Neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome (Orphanet:457185)
Perrault Syndrome (Orphanet:2855)
Perrault Syndrome 1 (OMIM:233400)
Polyneuropathy - hearing loss - ataxia - retinitis pigmentosa - cataract (Orphanet:171848)
REFSUM DISEASE, CLASSIC (OMIM:266500)
Refsum disease (Orphanet:773)
Ribose 5-phosphate isomerase deficiency (OMIM:608611)
Spinocerebellar ataxia type 12 (Orphanet:98762)
Spinocerebellar ataxia type 23 (Orphanet:101108)