About: Keratosis linearis with ichthyosis congenita and sclerosing keratoderma syndrome

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Medical condition

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dbo:description
  • medical condition (en)
  • медичний стан (uk)
dbo:icd10
  • Q82.8
dbo:medicalCause
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  • C566600
dbo:omim
  • 601952 (xsd:integer)
dbo:orpha
  • 281201
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  • This condition is inherited in an autosomal recessive manner. (en)
dbp:causes
  • Deletion in the POMP gene (en)
dbp:field
dbp:icd
  • (en)
  • Q82.8 (en)
dbp:meshid
  • 566600.0 (dbd:nicaraguanCórdoba)
dbp:name
  • Keratosis linearis with ichthyosis congenita and sclerosing keratoderma syndrome (en)
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  • 601952 (xsd:integer)
dbp:orphanet
  • 281201 (xsd:integer)
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  • Keratosis linearis with ichthyosis congenita and sclerosing keratoderma syndrome (en)
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foaf:name
  • Keratosis linearis with ichthyosis congenita and sclerosing keratoderma syndrome (en)
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