Onion bulb formation
Symptom Information:
Symptom ID: | HPO:0003383 | |||||||
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) Onion bulb formation(HPO:0003383) MedDRA: |
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Database Frequency: | 30 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
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 2M | (Orphanet:228179) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type A | (Orphanet:100043) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B | (Orphanet:100044) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E | (Orphanet:93114) |
Autosomal dominant intermediate Charcot-Marie-Tooth disease type F | (Orphanet:352670) |
Autosomal dominant slowed nerve conduction velocity | (Orphanet:140481) |
Autosomal recessive Charcot-Marie-Tooth disease with hoarseness | (Orphanet:101097) |
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A | (Orphanet:217055) |
Autosomal recessive spastic paraplegia type 55 | (Orphanet:320375) |
CHARCOT-MARIE-TOOTH DISEASE, RECESSIVE INTERMEDIATE D | (OMIM:616039) |
Charcot-Marie-Tooth disease type 1A | (Orphanet:101081) |
Charcot-Marie-Tooth disease type 1B | (Orphanet:101082) |
Charcot-Marie-Tooth disease type 1C | (Orphanet:101083) |
Charcot-Marie-Tooth disease type 1F | (Orphanet:101085) |
Charcot-Marie-Tooth disease type 2B1 | (Orphanet:98856) |
Charcot-Marie-Tooth disease type 4B2 | (Orphanet:99956) |
Charcot-Marie-Tooth disease type 4B3 | (Orphanet:363981) |
Charcot-Marie-Tooth disease type 4D | (Orphanet:99950) |
Charcot-Marie-Tooth disease type 4E | (Orphanet:99951) |
Charcot-Marie-Tooth disease type 4H | (Orphanet:99954) |
Charcot-Marie-Tooth disease type 4J | (Orphanet:139515) |
Corpus callosum agenesis - neuronopathy | (Orphanet:1496) |
Dejerine-Sottas syndrome | (Orphanet:64748) |
GIANT AXONAL NEUROPATHY 2, AUTOSOMAL DOMINANT | (OMIM:610100) |
Roussy-Lévy syndrome | (Orphanet:3115) |
Spastic paraplegia - neuropathy - poikiloderma | (Orphanet:2821) |
X-linked Charcot-Marie-Tooth disease type 1 | (Orphanet:101075) |
X-linked Charcot-Marie-Tooth disease type 5 | (Orphanet:99014) |