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| Fetal anomalies v8.26 | RPS15A | Ida Ertmanska commented on gene: RPS15A | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.25 | RPS15A | Esther Kinning reviewed gene: RPS15A: Rating: RED; Mode of pathogenicity: ; Publications: 27909223; Phenotypes: Diamond-Blackfan anemia 20, OMIM:618313; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.23 | RPS15A |
Ida Ertmanska gene: RPS15A was added gene: RPS15A was added to Fetal anomalies. Sources: NHS GMS,Expert Review Red Mode of inheritance for gene: RPS15A was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: RPS15A were set to 27909223 Phenotypes for gene: RPS15A were set to Diamond-Blackfan anemia 20, OMIM:618313 |
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