Decreased number of large peripheral myelinated nerve fibers
Symptom Information:
Symptom ID: | HPO:0003387 | ||||||
Synonyms: |
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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) Abnormal peripheral myelination(HPO:0003130) Decreased number of peripheral myelinated nerve fibers(HPO:0003380) Decreased number of large peripheral myelinated nerve fibers(HPO:0003387) MedDRA: |
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Database Frequency: | 11 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Ataxia - oculomotor apraxia type 1 | (Orphanet:1168) |
Autosomal dominant Charcot-Marie-Tooth disease type 2L | (Orphanet:99945) |
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A | (Orphanet:217055) |
Autosomal recessive intermediate Charcot-Marie-Tooth disease type C | (Orphanet:369867) |
Autosomal recessive spastic ataxia of Charlevoix-Saguenay | (Orphanet:98) |
Charcot-Marie-Tooth disease type 4C | (Orphanet:99949) |
Charcot-Marie-Tooth disease type 4F | (Orphanet:99952) |
Charcot-Marie-Tooth disease type 4G | (Orphanet:99953) |
Familial dysautonomia | (Orphanet:1764) |
Hereditary sensory and autonomic neuropathy type 1 | (Orphanet:36386) |
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA | (OMIM:162400) |