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Growth failure in early childhood v3.51 RIT1 Arina Puzriakova Phenotypes for gene: RIT1 were changed from Rasopathy; Noonan syndrome 8; Noonan syndrome type 8 to Noonan syndrome 8, OMIM:615355
Growth failure in early childhood v0.56 RIT1 Ivone Leong Publications for gene: RIT1 were set to
Growth failure in early childhood v0.27 RIT1 Rebecca Foulger reviewed gene: RIT1: Rating: AMBER; Mode of pathogenicity: Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments; Publications: 23791108, 25124994, 24939608; Phenotypes: Noonan syndrome 8, Noonan syndrome type 8; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Growth failure in early childhood v0.26 RIT1 Rebecca Foulger Mode of pathogenicity for gene RIT1 was changed from to Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments
Added phenotypes Noonan syndrome 8; Noonan syndrome type 8 for gene: RIT1
Growth failure in early childhood v0.1 RIT1 Ellen McDonagh gene: RIT1 was added
gene: RIT1 was added to Growth failure in early childhood. Sources: Expert Review Green
Mode of inheritance for gene: RIT1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes for gene: RIT1 were set to Rasopathy