Motor polyneuropathy

Symptom Information:

Symptom ID: HPO:0007178
Synonyms:
Peripheral motor neuropathy [HPO:0007178]
Peripheral neuropathy [Orphanet:43060]
Peripheral nerve disease (disorder) [Orphanet:43060]
Peripheral Neuropathy [Orphanet:43060]
Motor polyneuropathy [OMIM:Motor polyneuropathy]
Peripheral motor neuropathy [OMIM:Peripheral motor neuropathy]
Neuropathy peripheral [Orphanet:43060]
Neuropathy peripheral [MedDRA:10029331]
Hereditary and idiopathic peripheral neuropathy [MedDRA:10029331]
Hereditary and idiopathic peripheral neuropathy, other [MedDRA:10029331]
Inflammatory and toxic neuropathy [MedDRA:10029331]
Neuritis peripheral [MedDRA:10029331]
Neuropathy [MedDRA:10029331]
Neuropathy - (NOS) [MedDRA:10029331]
Neuropathy NOS [MedDRA:10029331]
Other hereditary and idiopathic peripheral neuropathy [MedDRA:10029331]
Other inflammatory and toxic neuropathies [MedDRA:10029331]
Other specified idiopathic peripheral neuropathy [MedDRA:10029331]
Peripheral neuritis [MedDRA:10029331]
Peripheral neuritis antepartum [MedDRA:10029331]
Peripheral neuritis in pregnancy [MedDRA:10029331]
Peripheral neuritis in pregnancy, unspecified as to episode of care [MedDRA:10029331]
Peripheral neuritis in pregnancy, with delivery [MedDRA:10029331]
Peripheral neuritis in pregnancy, with delivery, with mention of postpartum complication [MedDRA:10029331]
Peripheral neuritis NOS [MedDRA:10029331]
Peripheral neuritis postartum [MedDRA:10029331]
Peripheral neuropathy aggravated [MedDRA:10029331]
Peripheral neuropathy NOS [MedDRA:10029331]
Unspecified hereditary and idiopathic peripheral neuropathy [MedDRA:10029331]
Unspecified idiopathic peripheral neuropathy [MedDRA:10029331]
Unspecified inflammatory and toxic neuropathies [MedDRA:10029331]
Peripheral nerve disorder NOS [MedDRA:10029331]
Peripheral neuritis postpartum [MedDRA:10029331]
Cold sensitivity neuropathy [MedDRA:10029331]
Neuropathy (motor and sensory) [OMIM:Neuropathy (motor and sensory)]
No peripheral neuropathy [OMIM:No peripheral neuropathy]
Peripheral neuritis [OMIM:Peripheral neuritis]
Peripheral neuropathy (1 patient) [OMIM:Peripheral neuropathy (1 patient)]
Peripheral neuropathy (in some patients) [OMIM:Peripheral neuropathy (in some patients)]
Peripheral neuropathy (reported in 1 patient) [OMIM:Peripheral neuropathy (reported in 1 patient)]
Peripheral neuropathy (some patients) [OMIM:Peripheral neuropathy (some patients)]
Peripheral neuropathy (variable) [OMIM:Peripheral neuropathy (variable)]
Polyneuritis [MedDRA:10036104]
Neuritis (disorder) [Orphanet:43070]
Peripheral neuritis (disorder) [Orphanet:43070]
Polyneuritis (disorder) [Orphanet:43070]
Polyneuritis [Orphanet:43070]
Neuritis [Orphanet:43070]
Neuritis/polyneuritis/multineuritis [Orphanet:43070]
Polyneuritis [OMIM:Polyneuritis]
Neuritis [MedDRA:10029240]
Peripheral neuropathies [MedDRA:10034606]
Peripheral motor neuropathy [MedDRA:10034580]
Quality:
Cross references:
HPO:0003477 "Peripheral axonal neuropathy" [Orphanet:43060]
HPO:0009830 "Peripheral neuropathy" [Orphanet:43060]
Orphanet:43060 "Peripheral neuropathy" [Orphanet:43060]
Orphanet:43070 "Neuritis/polyneuritis/multineuritis" [Orphanet:43070]
OMIM: "Motor polyneuropathy" [OMIM:Motor polyneuropathy]
OMIM: "Peripheral motor neuropathy" [OMIM:Peripheral motor neuropathy]
OMIM: "Neuropathy (motor and sensory)" [OMIM:Neuropathy (motor and sensory)]
OMIM: "No peripheral neuropathy" [OMIM:No peripheral neuropathy]
OMIM: "Peripheral neuritis" [OMIM:Peripheral neuritis]
OMIM: "Peripheral neuropathy (1 patient)" [OMIM:Peripheral neuropathy (1 patient)]
OMIM: "Peripheral neuropathy (in some patients)" [OMIM:Peripheral neuropathy (in some patients)]
OMIM: "Peripheral neuropathy (reported in 1 patient)" [OMIM:Peripheral neuropathy (reported in 1 patient)]
OMIM: "Peripheral neuropathy (some patients)" [OMIM:Peripheral neuropathy (some patients)]
OMIM: "Peripheral neuropathy (variable)" [OMIM:Peripheral neuropathy (variable)]
OMIM: "Polyneuritis" [OMIM:Polyneuritis]
UMLS:C0031117 "Peripheral Neuropathy" [Orphanet:43060]
UMLS:C0032541 "Polyneuritis" [Orphanet:43070]
UMLS:C0027813 "Neuritis" [Orphanet:43070]
Is a (Direct Parents):
MedDRA Nervous system disorders
HPO         Peripheral neuropathy
Orphanet Functional anomalies of the nervous system
Orphanet Peripheral axonal neuropathy
MedDRA Peripheral neuropathies NEC
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)
    Peripheral axonal neuropathy(HPO:0003477)
       Peripheral neuropathies NEC(MedDRA:10034607)
          Motor polyneuropathy(HPO:0007178)
    Motor polyneuropathy(HPO:0007178)
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)