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Severe Paediatric Disorders v0.17 APOA1 Louise Daugherty Mode of inheritance for gene APOA1 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Severe Paediatric Disorders v0.12 APOA1 Louise Daugherty reviewed gene: APOA1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 APOA1 Louise Daugherty Publications for gene APOA1 were updated from to 30847515
Severe Paediatric Disorders v0.10 APOA1 Louise Daugherty Added phenotypes Amyloidosis, 3 or more types, 105200; ApoA-I and apoC-III deficiency, combined, 618463; Hypoalphalipoproteinemia, primary, 2, with or without corneal clouding, 618463 for gene: APOA1
Severe Paediatric Disorders v0.9 APOA1 Louise Daugherty Added phenotypes Amyloidosis, 3 or more types, 105200; ApoA-I and apoC-III deficiency, combined, 618463; Hypoalphalipoproteinemia, primary, 2, with or without corneal clouding, 618463 for gene: APOA1
Severe Paediatric Disorders v0.9 APOA1 Louise Daugherty Added phenotypes Amyloidosis, 3 or more types, 105200; ApoA-I and apoC-III deficiency, combined, 618463; Hypoalphalipoproteinemia, primary, 2, with or without corneal clouding, 618463 for gene: APOA1
Severe Paediatric Disorders v0.8 APOA1 Louise Daugherty Added phenotypes ApoA-I and apoC-III deficiency, combined, 618463; Hypoalphalipoproteinemia, primary, 2, with or without corneal clouding, 618463; Amyloidosis, 3 or more types, 105200 for gene: APOA1
Severe Paediatric Disorders v0.7 APOA1 Louise Daugherty Source Next Generation Children Project was added to APOA1.
Severe Paediatric Disorders v0.5 APOA1 Louise Daugherty Source Expert Review Green was added to APOA1.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 APOA1 Louise Daugherty gene: APOA1 was added
gene: APOA1 was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: APOA1 was set to