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Structural eye disease v3.75 | IKBKG | Arina Puzriakova Phenotypes for gene: IKBKG were changed from Incontinentia pigmenti, IP, 308300 to Incontinentia pigmenti, OMIM:308300 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Structural eye disease v0.91 | IKBKG | Nicola Ragge reviewed gene: IKBKG: Rating: RED; Mode of pathogenicity: ; Publications: 31119873, 20499493, 30905793 ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Structural eye disease v0.89 | IKBKG |
Ivone Leong Source NHS GMS was added to IKBKG. Source Expert Review Red was added to IKBKG. Publications for gene IKBKG were changed from to 31119873; 20499493; 30905793 Rating Changed from Amber List (moderate evidence) to Red List (low evidence) |
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Structural eye disease v0.88 | IKBKG |
Ivone Leong Source Expert Review Amber was added to IKBKG. Rating Changed from Red List (low evidence) to Amber List (moderate evidence) |
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Structural eye disease v0.60 | IKBKG | Mariya Moosajee reviewed gene: IKBKG: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Incontinentia pigmenti, IP; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Structural eye disease v0.59 | IKBKG |
Ivone Leong gene: IKBKG was added gene: IKBKG was added to Structural eye disease. Sources: London North GLH Mode of inheritance for gene: IKBKG was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females Phenotypes for gene: IKBKG were set to Incontinentia pigmenti, IP, 308300 |