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| DDG2P v3.12 | ALX1 | Achchuthan Shanmugasundram reviewed gene: ALX1: Rating: GREEN; Mode of pathogenicity: ; Publications: 20451171, 27324866; Phenotypes: FRONTONASAL DYSPLASIA TYPE 3, OMIM:613456; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| DDG2P v0.2 | ALX1 | Rebecca Foulger reviewed gene: ALX1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| DDG2P v0.1 | ALX1 |
Rebecca Foulger gene: ALX1 was added gene: ALX1 was added to DDG2P. Sources: Expert Review Green,DD-Gene2Phenotype Mode of inheritance for gene: ALX1 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: ALX1 were set to 20451171; 27324866 Phenotypes for gene: ALX1 were set to FRONTONASAL DYSPLASIA TYPE 3 136760 |
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