Decreased number of peripheral myelinated nerve fibers

Symptom Information:

Symptom ID: HPO:0003380
Synonyms:
Decreased number of large and small myelinated fibers [HPO:0003380]
Loss of myelinated fibers [HPO:0003380]
Decreased number of large and small myelinated fibers [OMIM:Decreased number of large and small myelinated fibers]
Loss of myelinated fibers [OMIM:Loss of myelinated fibers]
Quality:
Cross references:
OMIM: "Decreased number of large and small myelinated fibers" [OMIM:Decreased number of large and small myelinated fibers]
OMIM: "Loss of myelinated fibers" [OMIM:Loss of myelinated fibers]
Is a (Direct Parents):
HPO         Abnormal peripheral myelination
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)
MedDRA:
Database Frequency: 30 / 7739
Resource:

All diseases associated with this symptom:

46,XY gonadal dysgenesis - motor and sensory neuropathy (Orphanet:168563)
Autosomal dominant Charcot-Marie-Tooth disease type 2A1 (Orphanet:99946)
Autosomal dominant Charcot-Marie-Tooth disease type 2A2 (Orphanet:99947)
Autosomal dominant Charcot-Marie-Tooth disease type 2B (Orphanet:99936)
Autosomal dominant Charcot-Marie-Tooth disease type 2G (Orphanet:99941)
Autosomal dominant Charcot-Marie-Tooth disease type 2I (Orphanet:99942)
Autosomal dominant Charcot-Marie-Tooth disease type 2K (Orphanet:99944)
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B (Orphanet:100044)
Autosomal recessive Charcot-Marie-Tooth disease with hoarseness (Orphanet:101097)
Autosomal recessive spastic paraplegia type 11 (Orphanet:2822)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2R (OMIM:615490)
Charcot-Marie-Tooth disease type 1A (Orphanet:101081)
Charcot-Marie-Tooth disease type 1B (Orphanet:101082)
Charcot-Marie-Tooth disease type 1F (Orphanet:101085)
Charcot-Marie-Tooth disease type 2B1 (Orphanet:98856)
Charcot-Marie-Tooth disease type 2H (Orphanet:101102)
Charcot-Marie-Tooth disease type 4A (Orphanet:99948)
Charcot-Marie-Tooth disease type 4B2 (Orphanet:99956)
Charcot-Marie-Tooth disease type 4H (Orphanet:99954)
Dejerine-Sottas syndrome (Orphanet:64748)
Giant axonal neuropathy (Orphanet:643)
Hereditary motor and sensory neuropathy, Okinawa type (Orphanet:90117)
Hereditary sensory and autonomic neuropathy type 2 (Orphanet:970)
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, ADULT-ONSET, WITH ANOSMIA (OMIM:608720)
NEUROPATHY, HEREDITARY SENSORY, TYPE IE (OMIM:614116)
NEUROPATHY, HEREDITARY SENSORY, X-LINKED (OMIM:310470)
Navajo neurohepatopathy (Orphanet:255229)
Roussy-Lévy syndrome (Orphanet:3115)
Spinocerebellar ataxia type 25 (Orphanet:101111)
X-linked Charcot-Marie-Tooth disease type 1 (Orphanet:101075)