Decreased number of large peripheral myelinated nerve fibers

Symptom Information:

Symptom ID: HPO:0003387
Synonyms:
Depletion of large myelinated fibers [HPO:0003387]
Loss of large myelinated fibers [HPO:0003387]
Loss of larger myelinated nerve fibers [HPO:0003387]
Depletion of large myelinated fibers [OMIM:Depletion of large myelinated fibers]
Loss of large myelinated fibers [OMIM:Loss of large myelinated fibers]
Loss of larger myelinated nerve fibers [OMIM:Loss of larger myelinated nerve fibers]
Quality:
Cross references:
OMIM: "Depletion of large myelinated fibers" [OMIM:Depletion of large myelinated fibers]
OMIM: "Loss of large myelinated fibers" [OMIM:Loss of large myelinated fibers]
OMIM: "Loss of larger myelinated nerve fibers" [OMIM:Loss of larger myelinated nerve fibers]
Is a (Direct Parents):
HPO         Decreased number of peripheral myelinated nerve fibers
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:
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)