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Haemophagocytic syndrome with absent XIAP expression v1.3 XIAP Achchuthan Shanmugasundram Added comment: Comment on phenotypes: This gene has been associated with MIM #300635 in OMIM and the OMIM record was last accessed on 20 December 2025.
Haemophagocytic syndrome with absent XIAP expression v1.3 XIAP Achchuthan Shanmugasundram Phenotypes for gene: XIAP were changed from Lymphoproliferative syndrome, X-linked, 2, OMIM:300635; X-linked lymphoproliferative disease due to XIAP deficiency, MONDO:0010385 to Lymphoproliferative syndrome, X-linked, 2, OMIM:300635; X-linked lymphoproliferative disease due to XIAP deficiency, MONDO:0010385
Haemophagocytic syndrome with absent XIAP expression v1.2 XIAP Achchuthan Shanmugasundram Phenotypes for gene: XIAP were changed from to Lymphoproliferative syndrome, X-linked, 2, OMIM:300635; X-linked lymphoproliferative disease due to XIAP deficiency, MONDO:0010385
Haemophagocytic syndrome with absent XIAP expression v0.1 XIAP Achchuthan Shanmugasundram reviewed gene: XIAP: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Haemophagocytic syndrome with absent XIAP expression v0.1 XIAP Achchuthan Shanmugasundram gene: XIAP was added
gene: XIAP was added to Haemophagocytic syndrome with absent XIAP expression. Sources: NHS GMS,Expert Review Green
Mode of inheritance for gene: XIAP was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Haemophagocytic syndrome with absent XIAP expression v0.0 Achchuthan Shanmugasundram Added Panel Haemophagocytic syndrome with absent XIAP expression
Set list of related panels to R18
Set panel types to: GMS Rare Disease