Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Vitamin metabolism disorders v1.2 | ALDH1A3 |
Bryony Thompson gene: ALDH1A3 was added gene: ALDH1A3 was added to Vitamin metabolism disorders. Sources: Expert Review Red Mode of inheritance for gene: ALDH1A3 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: ALDH1A3 were set to 23312594, 23591992, 30200890 Phenotypes for gene: ALDH1A3 were set to Isolated microphthalmia 8 MONDO:0014050; Other disorders of vitamin metabolism |