Kerion celsi
General Information (adopted from Orphanet):
Synonyms, Signs: |
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Number of Symptoms | 10 |
OrphanetNr: | 499 |
OMIM Id: |
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ICD-10: |
B35.0 |
UMLs: |
C0276742 |
MeSH: |
C536165 |
MedDRA: |
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Snomed: |
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Prevalence, inheritance and age of onset:
Prevalence: | No data available. |
Inheritance: |
Not applicable [Orphanet] |
Age of onset: |
All ages [Orphanet] |
Disease classification (adopted from Orphanet):
Parent Diseases: |
Other acquired skin disease
-Rare skin disease |
Symptom Information:
|
(HPO:0002315) | Headache | Occasional [Orphanet] | 175 / 7739 | |||
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(HPO:0001596) | Alopecia | Frequent [Orphanet] | 162 / 7739 | |||
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(HPO:0011123) | Inflammatory abnormality of the skin | Very frequent [Orphanet] | 10 / 7739 | |||
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(HPO:0100838) | Recurrent cutaneous abscess formation | Very frequent [Orphanet] | 15 / 7739 | |||
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(HPO:0010720) | Abnormal hair pattern | Very frequent [Orphanet] | 14 / 7739 | |||
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(HPO:0200042) | Skin ulcer | Very frequent [Orphanet] | 138 / 7739 | |||
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(HPO:0001945) | Fever | Frequent [Orphanet] | 218 / 7739 | |||
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(HPO:0002716) | Lymphadenopathy | Frequent [Orphanet] | 129 / 7739 | |||
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(HPO:0003326) | Myalgia | Occasional [Orphanet] | 143 / 7739 | |||
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(HPO:0030350) | Erythematous papule | Very frequent [Orphanet] | 123 / 7739 |
Associated genes:
ClinVar (via SNiPA)
Gene symbol | Variation | Clinical significance | Reference |
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