Onion bulb formation

Symptom Information:

Symptom ID: HPO:0003383
Synonyms:
'Onion bulb' formations [HPO:0003383]
ONION BULB FORMATIONS [HPO:0003383]
'Onion bulb' formations [OMIM:'Onion bulb' formations]
Onion bulb formation [OMIM:Onion bulb formation]
Onion bulb formations [OMIM:Onion bulb formations]
'Onion bulb' formations (rare) [OMIM:'Onion bulb' formations (rare)]
'Onion' bulb formation [OMIM:'Onion' bulb formation]
Quality:
Cross references:
OMIM: "'Onion bulb' formations" [OMIM:'Onion bulb' formations]
OMIM: "Onion bulb formation" [OMIM:Onion bulb formation]
OMIM: "Onion bulb formations" [OMIM:Onion bulb formations]
OMIM: "'Onion bulb' formations (rare)" [OMIM:'Onion bulb' formations (rare)]
OMIM: "'Onion' bulb formation" [OMIM:'Onion' bulb formation]
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)
                   Onion bulb formation(HPO:0003383)
MedDRA:
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)