Decreased number of peripheral myelinated nerve fibers
Symptom Information:
Symptom ID: | HPO:0003380 | ||||
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) Abnormal peripheral myelination(HPO:0003130) Decreased number of peripheral myelinated nerve fibers(HPO:0003380) MedDRA: |
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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) |