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Severe Paediatric Disorders v1.101 NOD2 Arina Puzriakova Phenotypes for gene: NOD2 were changed from Blau syndrome, 186580 to Blau syndrome, OMIM:186580; {Inflammatory bowel disease 1, Crohn disease}, OMIM:266600; {Yao syndrome}, OMIM:617321
Severe Paediatric Disorders v0.12 NOD2 Louise Daugherty reviewed gene: NOD2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 NOD2 Louise Daugherty Publications for gene NOD2 were updated from to 30847515
Severe Paediatric Disorders v0.11 NOD2 Louise Daugherty Mode of inheritance for gene NOD2 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Severe Paediatric Disorders v0.10 NOD2 Louise Daugherty Added phenotypes Blau syndrome, 186580 for gene: NOD2
Severe Paediatric Disorders v0.9 NOD2 Louise Daugherty Added phenotypes Blau syndrome, 186580 for gene: NOD2
Severe Paediatric Disorders v0.9 NOD2 Louise Daugherty Added phenotypes Blau syndrome, 186580 for gene: NOD2
Severe Paediatric Disorders v0.8 NOD2 Louise Daugherty Added phenotypes Blau syndrome, 186580 for gene: NOD2
Severe Paediatric Disorders v0.7 NOD2 Louise Daugherty Source Next Generation Children Project was added to NOD2.
Severe Paediatric Disorders v0.5 NOD2 Louise Daugherty Source Expert Review Green was added to NOD2.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 NOD2 Louise Daugherty gene: NOD2 was added
gene: NOD2 was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: NOD2 was set to