Keratosis pilaris atrophicans
General Information (adopted from Orphanet):
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Synonyms, Signs:
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Number of Symptoms
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8
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OrphanetNr:
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498
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OMIM Id:
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ICD-10:
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L85.8
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UMLs:
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MeSH:
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MedDRA:
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Snomed:
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400059005
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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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Disease classification (adopted from Orphanet):
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Parent Diseases:
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Other epidermis disorder
-Rare skin disease
Other genetic epidermal disease
-Rare genetic disease
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1
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(HPO:0011123)
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Inflammatory abnormality of the skin |
Occasional [Orphanet]
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10 / 7739
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2
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(HPO:0008064)
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Ichthyosis |
Occasional [Orphanet]
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108 / 7739
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3
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(HPO:0000962)
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Hyperkeratosis |
Very frequent [Orphanet]
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216 / 7739
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4
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(HPO:0000989)
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Pruritus |
Occasional [Orphanet]
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111 / 7739
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5
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(HPO:0000958)
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Dry skin |
Frequent [Orphanet]
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152 / 7739
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6
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(HPO:0002099)
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Asthma |
Occasional [Orphanet]
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62 / 7739
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7
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(HPO:0100326)
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Immunologic hypersensitivity |
Frequent [Orphanet]
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28 / 7739
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8
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(HPO:0030350)
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Erythematous papule |
Very frequent [Orphanet]
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123 / 7739
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ClinVar (via SNiPA)
| Gene symbol |
Variation |
Clinical significance |
Reference |