Motor axonal neuropathy

Symptom Information:

Symptom ID: HPO:0007002
Synonyms:
Motor axonal neuropathy [OMIM:Motor axonal neuropathy]
Axonal motor neuropathy [OMIM:Axonal motor neuropathy]
Axonal motor neuropathy (in about 50%) [OMIM:Axonal motor neuropathy (in about 50%)]
Axonal motor neuropathy (lower limbs more affected than upper limbs) [OMIM:Axonal motor neuropathy (lower limbs more affected than upper limbs)]
Quality:
Cross references:
OMIM: "Motor axonal neuropathy" [OMIM:Motor axonal neuropathy]
OMIM: "Axonal motor neuropathy" [OMIM:Axonal motor neuropathy]
OMIM: "Axonal motor neuropathy (in about 50%)" [OMIM:Axonal motor neuropathy (in about 50%)]
OMIM: "Axonal motor neuropathy (lower limbs more affected than upper limbs)" [OMIM:Axonal motor neuropathy (lower limbs more affected than upper limbs)]
Is a (Direct Parents):
HPO         Peripheral axonal 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)
                      Motor axonal neuropathy(HPO:0007002)
                Peripheral axonal degeneration(HPO:0000764)
                   Peripheral axonal neuropathy(HPO:0003477)
                      Motor axonal neuropathy(HPO:0007002)
MedDRA:
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

ACHALASIA-ADDISONIANISM-ALACRIMA SYNDROME (OMIM:231550)
Autosomal dominant spastic paraplegia type 31 (Orphanet:101011)
Autosomal dominant spastic paraplegia type 9 (Orphanet:100990)
Autosomal recessive axonal neuropathy with neuromyotonia (Orphanet:324442)
Autosomal recessive spastic paraplegia type 14 (Orphanet:100995)
Autosomal recessive spastic paraplegia type 46 (Orphanet:320391)
CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED, WITH APLASIACUTIS CONGENITA (OMIM:302803)
Giant axonal neuropathy (Orphanet:643)
MERRF (Orphanet:551)
McLeod neuroacanthocytosis syndrome (Orphanet:59306)
NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 6 (OMIM:615643)
Neurodegeneration with brain iron accumulation due to C19orf12 mutation (Orphanet:289560)
PONTOCEREBELLAR HYPOPLASIA, TYPE 1B (OMIM:614678)
Palmoplantar keratoderma-spastic paralysis syndrome (Orphanet:2201)
Spastic paraplegia-optic atrophy-neuropathy syndrome (Orphanet:320406)
Triple A syndrome (Orphanet:869)
X-linked Charcot-Marie-Tooth disease type 4 (Orphanet:101078)