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| Congenital Heart Defect v1.31 | PFKP | Rylee Peters Marked gene: PFKP as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital Heart Defect v1.31 | PFKP | Rylee Peters Gene: pfkp has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital Heart Defect v1.31 | Rylee Peters Copied gene PFKP from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital Heart Defect v1.31 | PFKP |
Rylee Peters gene: PFKP was added gene: PFKP was added to Congenital Heart Defect. Sources: Expert Review Amber,Literature Mode of inheritance for gene: PFKP was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: PFKP were set to 42385441 Phenotypes for gene: PFKP were set to Congenital heart disease, MONDO:0005453, PFKP-related |
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