Motor polyneuropathy
Symptom Information:
Symptom ID: | HPO:0007178 | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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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) Motor polyneuropathy(HPO:0007178) MedDRA: Nervous system disorders(MedDRA:10029205) Motor polyneuropathy(HPO:0007178) Peripheral axonal neuropathy(HPO:0003477) Peripheral neuropathies NEC(MedDRA:10034607) Motor polyneuropathy(HPO:0007178) |
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Database Frequency: | 31 / 7739 | |||||||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AMYLOIDOSIS, PRIMARY LOCALIZED CUTANEOUS, 1 | (OMIM:105250) |
ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTICATROPHY AND MENTAL RETARDATION | (OMIM:270500) |
Adult polyglucosan body disease | (Orphanet:206583) |
Autosomal dominant spastic paraplegia type 9 | (Orphanet:100990) |
Autosomal recessive spastic paraplegia type 11 | (Orphanet:2822) |
Autosomal recessive spastic paraplegia type 46 | (Orphanet:320391) |
Autosomal recessive spastic paraplegia type 48 | (Orphanet:306511) |
BROWN-VIALETTO-VAN LAERE SYNDROME 1 | (OMIM:211530) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
CADASIL | (Orphanet:136) |
CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURALHEARING LOSS | (OMIM:601338) |
Cervical hypertrichosis - peripheral neuropathy | (Orphanet:2218) |
Combined oxidative phosphorylation defect type 11 | (Orphanet:324535) |
Congenital cataracts - facial dysmorphism - neuropathy | (Orphanet:48431) |
Corpus callosum agenesis - neuronopathy | (Orphanet:1496) |
DEND syndrome | (Orphanet:79134) |
Flynn-Aird syndrome | (Orphanet:2047) |
ICHTHYOSIS AND MALE HYPOGONADISMRUD SYNDROME, INCLUDED | (OMIM:308200) |
Leukoencephalopathy - ataxia - hypodontia - hypomyelination | (Orphanet:137639) |
MELAS | (Orphanet:550) |
MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE | (OMIM:300861) |
MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY | (OMIM:614741) |
Navajo neurohepatopathy | (Orphanet:255229) |
Odontoleukodystrophy | (Orphanet:77295) |
Permanent neonatal diabetes mellitus | (Orphanet:99885) |
Porphyria due to ALA dehydratase deficiency | (Orphanet:100924) |
Primary hyperoxaluria type 1 | (Orphanet:93598) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
SCAPULOPERONEAL SPINAL MUSCULAR ATROPHY | (OMIM:181405) |
Tangier disease | (Orphanet:31150) |
Wolfram syndrome | (Orphanet:3463) |