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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Hereditary skin disorder
/
Inherited ichthyosis
/
Peeling skin syndrome
Peeling skin syndrome 6
rare
Identifiers
MONDO:0054852
OMIM:618084
Causal genes
FLG2
Part of
Peeling skin syndrome
Also known as
PSS6
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