Sensory axonal neuropathy

Symptom Information:

Symptom ID: HPO:0003390
Synonyms:
Axonal sensory neuropathy [HPO:0003390]
Peripheral sensory axonal neuropathy [HPO:0003390]
Axonal sensory neuropathy [OMIM:Axonal sensory neuropathy]
Peripheral sensory axonal neuropathy [OMIM:Peripheral sensory axonal neuropathy]
Sensory axonal neuropathy [OMIM:Sensory axonal neuropathy]
Axonal sensory neuropathy (less common) [OMIM:Axonal sensory neuropathy (less common)]
Axonal sensory neuropathy (lower limbs more affected than upper limbs) [OMIM:Axonal sensory neuropathy (lower limbs more affected than upper limbs)]
Quality:
Cross references:
OMIM: "Axonal sensory neuropathy" [OMIM:Axonal sensory neuropathy]
OMIM: "Peripheral sensory axonal neuropathy" [OMIM:Peripheral sensory axonal neuropathy]
OMIM: "Sensory axonal neuropathy" [OMIM:Sensory axonal neuropathy]
OMIM: "Axonal sensory neuropathy (less common)" [OMIM:Axonal sensory neuropathy (less common)]
OMIM: "Axonal sensory neuropathy (lower limbs more affected than upper limbs)" [OMIM:Axonal sensory neuropathy (lower limbs more affected than upper limbs)]
Is a (Direct Parents):
HPO         Peripheral axonal neuropathy
HPO         Sensory 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)
                   Peripheral axonal neuropathy(HPO:0003477)
                      Sensory axonal neuropathy(HPO:0003390)
                   Sensory neuropathy(HPO:0000763)
                      Sensory axonal neuropathy(HPO:0003390)
                Peripheral axonal degeneration(HPO:0000764)
                   Peripheral axonal neuropathy(HPO:0003477)
                      Sensory axonal neuropathy(HPO:0003390)
MedDRA:
Database Frequency: 26 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant progressive external ophthalmoplegia (Orphanet:254892)
Autosomal dominant spastic paraplegia type 3 (Orphanet:100984)
Autosomal recessive axonal neuropathy with neuromyotonia (Orphanet:324442)
Autosomal recessive progressive external ophthalmoplegia (Orphanet:254886)
Autosomal recessive spastic paraplegia type 11 (Orphanet:2822)
CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED, WITH APLASIACUTIS CONGENITA (OMIM:302803)
EPILEPSY, PROGRESSIVE MYOCLONIC, 1B (OMIM:612437)
Giant axonal neuropathy (Orphanet:643)
Hereditary sensory and autonomic neuropathy type 1B (Orphanet:139564)
Infantile onset spinocerebellar ataxia (Orphanet:1186)
MERRF (Orphanet:551)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
NEUROPATHY, HEREDITARY SENSORY, TYPE IF (OMIM:615632)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 1 (OMIM:157640)
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 3 (OMIM:609286)
Palmoplantar keratoderma-spastic paralysis syndrome (Orphanet:2201)
Pelizaeus-Merzbacher-like due to GJC2 mutation (Orphanet:280282)
Perrault Syndrome 5 (OMIM:616138)
Sensory ataxic neuropathy-dysarthria-ophthalmoparesis (Orphanet:70595)
Severe X-linked mitochondrial encephalomyopathy (Orphanet:238329)
Spastic paraplegia-optic atrophy-neuropathy syndrome (Orphanet:320406)
Spinocerebellar ataxia type 18 (Orphanet:98771)
Spinocerebellar ataxia type 27 (Orphanet:98764)
Spinocerebellar ataxia with epilepsy (Orphanet:254881)
X-linked Charcot-Marie-Tooth disease type 4 (Orphanet:101078)
X-linked hereditary sensory and autonomic neuropathy with deafness (Orphanet:139583)