Peripheral axonal neuropathy

Symptom Information:

Symptom ID: HPO:0003477
Synonyms:
Axonal neuropathy [HPO:0003477]
Axonal peripheral neuropathy [HPO:0003477]
Peripheral neuropathy [Orphanet:43060]
Peripheral nerve disease (disorder) [Orphanet:43060]
Peripheral Neuropathy [Orphanet:43060]
Axonal neuropathy [OMIM:Axonal neuropathy]
Axonal peripheral neuropathy [OMIM:Axonal peripheral neuropathy]
Peripheral axonal neuropathy [OMIM:Peripheral axonal 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]
Axonal neuropathy (in 2 of 3 families) [OMIM:Axonal neuropathy (in 2 of 3 families)]
Axonal neuropathy (in some patients) [OMIM:Axonal neuropathy (in some patients)]
Axonal neuropathy (rare) [OMIM:Axonal neuropathy (rare)]
Neuropathy (motor and sensory) [OMIM:Neuropathy (motor and sensory)]
No peripheral neuropathy [OMIM:No peripheral neuropathy]
Peripheral axonal neuropathy (in some patients) [OMIM:Peripheral axonal neuropathy (in some patients)]
Peripheral axonal neuropathy (uncommon) [OMIM:Peripheral axonal neuropathy (uncommon)]
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]
Axonal neuropathy [MedDRA:10003882]
Quality:
Cross references:
HPO:0009830 "Peripheral neuropathy" [Orphanet:43060]
HPO:0007178 "Motor polyneuropathy" [Orphanet:43060]
Orphanet:43060 "Peripheral neuropathy" [Orphanet:43060]
Orphanet:43070 "Neuritis/polyneuritis/multineuritis" [Orphanet:43070]
OMIM: "Axonal neuropathy" [OMIM:Axonal neuropathy]
OMIM: "Axonal peripheral neuropathy" [OMIM:Axonal peripheral neuropathy]
OMIM: "Peripheral axonal neuropathy" [OMIM:Peripheral axonal neuropathy]
OMIM: "Axonal neuropathy (in 2 of 3 families)" [OMIM:Axonal neuropathy (in 2 of 3 families)]
OMIM: "Axonal neuropathy (in some patients)" [OMIM:Axonal neuropathy (in some patients)]
OMIM: "Axonal neuropathy (rare)" [OMIM:Axonal neuropathy (rare)]
OMIM: "Neuropathy (motor and sensory)" [OMIM:Neuropathy (motor and sensory)]
OMIM: "No peripheral neuropathy" [OMIM:No peripheral neuropathy]
OMIM: "Peripheral axonal neuropathy (in some patients)" [OMIM:Peripheral axonal neuropathy (in some patients)]
OMIM: "Peripheral axonal neuropathy (uncommon)" [OMIM:Peripheral axonal neuropathy (uncommon)]
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 Peripheral neuropathies NEC
HPO         Peripheral axonal degeneration
HPO         Peripheral neuropathy
MedDRA Nervous system disorders
Orphanet Functional anomalies of the nervous system
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)
                   Peripheral axonal neuropathy(HPO:0003477)
                Peripheral axonal degeneration(HPO:0000764)
                   Peripheral axonal neuropathy(HPO:0003477)
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Peripheral axonal neuropathy(HPO:0003477)
Database Frequency: 62 / 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)
ATTRV122I amyloidosis (Orphanet:85451)
Adult polyglucosan body disease (Orphanet:206583)
Alpha-N-acetylgalactosaminidase deficiency type 2 (Orphanet:79280)
Autosomal dominant Charcot-Marie-Tooth disease type 2L (Orphanet:99945)
Autosomal dominant Charcot-Marie-Tooth disease type 2N (Orphanet:228174)
Autosomal recessive cerebellar ataxia - saccadic intrusion (Orphanet:95434)
Autosomal recessive spastic paraplegia type 11 (Orphanet:2822)
Autosomal recessive spastic paraplegia type 15 (Orphanet:100996)
Autosomal recessive spastic paraplegia type 28 (Orphanet:101008)
Autosomal recessive spastic paraplegia type 30 (Orphanet:101010)
Autosomal recessive spastic paraplegia type 55 (Orphanet:320375)
BROWN-VIALETTO-VAN LAERE SYNDROME 1 (OMIM:211530)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
CADASIL (Orphanet:136)
CARDIOFACIOCUTANEOUS SYNDROME 1 (OMIM:115150)
CARDIOFACIOCUTANEOUS SYNDROME 2 (OMIM:615278)
CEREBELLAR ATAXIA, AREFLEXIA, PES CAVUS, OPTIC ATROPHY, AND SENSORINEURALHEARING LOSS (OMIM:601338)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R (OMIM:615490)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2U (OMIM:616280)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Combined oxidative phosphorylation defect type 11 (Orphanet:324535)
Corpus callosum agenesis - neuronopathy (Orphanet:1496)
DEND syndrome (Orphanet:79134)
EAST syndrome (Orphanet:199343)
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULARINVOLVEMENT (OMIM:600638)
Familial amyloid polyneuropathy (Orphanet:85447)
Flynn-Aird syndrome (Orphanet:2047)
GIANT AXONAL NEUROPATHY 2, AUTOSOMAL DOMINANT (OMIM:610100)
Glycogen storage disease due to glycogen debranching enzyme deficiency (Orphanet:366)
Hereditary angioedema type 1 (Orphanet:100050)
Hereditary motor and sensory neuropathy type 5 (Orphanet:64751)
Hereditary sensory and autonomic neuropathy with spastic paraplegia (Orphanet:139578)
ICHTHYOSIS AND MALE HYPOGONADISMRUD SYNDROME, INCLUDED (OMIM:308200)
Leukoencephalopathy - ataxia - hypodontia - hypomyelination (Orphanet:137639)
Leukoencephalopathy with brain stem and spinal cord involvement - lactate elevation (Orphanet:137898)
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (Orphanet:5)
MELAS (Orphanet:550)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 13 (OMIM:614563)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 9 (OMIM:614255)
MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE (OMIM:300861)
MITOCHONDRIAL PYRUVATE CARRIER DEFICIENCY (OMIM:614741)
MONONEUROPATHY OF THE MEDIAN NERVE, MILD (OMIM:613353)
Metatropic dysplasia (Orphanet:2635)
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIB (OMIM:613115)
NEUROPATHY, HEREDITARY SENSORY, TYPE ID (OMIM:613708)
Odontoleukodystrophy (Orphanet:77295)
Permanent neonatal diabetes mellitus (Orphanet:99885)
Perrault Syndrome 5 (OMIM:616138)
Pontocerebellar hypoplasia, type 9 (OMIM:615809)
Porphyria due to ALA dehydratase deficiency (Orphanet:100924)
Primary hyperoxaluria type 1 (Orphanet:93598)
Progressive demyelinating neuropathy with bilateral striatal necrosis (Orphanet:217396)
Pyruvate dehydrogenase E1-alpha deficiency (Orphanet:79243)
Rabson-Mendenhall syndrome (Orphanet:769)
SPINOCEREBELLAR ATAXIA 38 (OMIM:615957)
Spinocerebellar ataxia type 1 with axonal neuropathy (Orphanet:94124)
Spinocerebellar ataxia with axonal neuropathy type 2 (Orphanet:64753)
Tangier disease (Orphanet:31150)
Trichomegaly - retina pigmentary degeneration - dwarfism (Orphanet:3363)
Wolfram syndrome (Orphanet:3463)