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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
Inflammatory poikiloderma with hair abnormalities and acral keratoses
rare
Identifiers
MONDO:0859355
OMIM:620199
Causal genes
LTV1
Part of
Hereditary poikiloderma
Hereditary skin disorder
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