Sensorimotor neuropathy
Symptom Information:
Symptom ID: | HPO:0007141 | ||||||||
Synonyms: |
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Quality: | |||||||||
Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |