Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Vitamin metabolism disorders v1.2 | RDH12 |
Bryony Thompson gene: RDH12 was added gene: RDH12 was added to Vitamin metabolism disorders. Sources: Expert Review Green Mode of inheritance for gene: RDH12 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: RDH12 were set to 15322982; 16269441 Phenotypes for gene: RDH12 were set to Leber congenital amaurosis 13 MONDO:0012990; Other disorders of vitamin metabolism |