Proliferating trichilemmal cyst
General Information (adopted from Orphanet):
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Synonyms, Signs:
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Number of Symptoms
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4
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OrphanetNr:
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492
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OMIM Id:
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ICD-10:
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L72.1
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UMLs:
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MeSH:
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MedDRA:
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Snomed:
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Prevalence, inheritance and age of onset:
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Prevalence:
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No data available.
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Inheritance:
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Autosomal dominant inheritance
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Age of onset:
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Adult
[Orphanet]
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Disease classification (adopted from Orphanet):
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Parent Diseases:
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Rare skin tumor or hamartoma
-Rare oncologic disease
-Rare skin disease
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1
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(HPO:0001965)
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Abnormality of the scalp |
Very frequent [Orphanet]
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10 / 7739
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2
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(HPO:0008069)
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Neoplasm of the skin |
Very frequent [Orphanet]
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84 / 7739
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3
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(HPO:0001006)
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Hypotrichosis |
Frequent [Orphanet]
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219 / 7739
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4
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(HPO:0200042)
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Skin ulcer |
Very frequent [Orphanet]
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138 / 7739
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ClinVar (via SNiPA)
| Gene symbol |
Variation |
Clinical significance |
Reference |