Syndromic recessive X-linked ichthyosis

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Name:
Syndromic recessive X-linked ichthyosis
Description:
A rare genetic skin disease belonging to the Mendelian Disorders of Cornification (MeDOC) characterized by a generally mild cutaneous desquamation in association with extracutaneous manifestations as part of a syndrome.
ORPHAcode:
281090
Synonyms:
Recessive X-linked ichthyosis with extracutaneous manifestations
Syndromic RXLI
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14