Motor axonal neuropathy
Symptom Information:
Symptom ID: | HPO:0007002 | ||||
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 axonal degeneration(HPO:0000764) Peripheral axonal neuropathy(HPO:0003477) Motor axonal neuropathy(HPO:0007002) Peripheral neuropathy(HPO:0009830) Peripheral axonal neuropathy(HPO:0003477) Motor axonal neuropathy(HPO:0007002) MedDRA: |
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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) |