Erythroderma desquamativum
General Information (adopted from Orphanet):
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Synonyms, Signs:
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Leiner disease
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Number of Symptoms
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4
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OrphanetNr:
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314
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OMIM Id:
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ICD-10:
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L21.1
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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
Autosomal recessive 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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Genetic immune deficiency with skin involvement
-Rare genetic disease
Immune deficiency with skin involvement
-Rare skin disease
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1
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(HPO:0002024)
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Malabsorption |
Very frequent [Orphanet]
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142 / 7739
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2
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(HPO:0004325)
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Decreased body weight |
Very frequent [Orphanet]
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492 / 7739
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3
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(HPO:0001051)
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Seborrheic dermatitis |
Very frequent [Orphanet]
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25 / 7739
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4
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(HPO:0010978)
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Abnormality of immune system physiology |
Very frequent [Orphanet]
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148 / 7739
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ClinVar (via SNiPA)
| Gene symbol |
Variation |
Clinical significance |
Reference |