Activity
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| Fetal anomalies v8.26 | FGD5 | Ida Ertmanska commented on gene: FGD5 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.25 | FGD5 | Louise Carr reviewed gene: FGD5: Rating: AMBER; Mode of pathogenicity: ; Publications: 41574350, 41199744, 30232381, 32037394; Phenotypes: Congenital heart disease, tetralogy of Fallout (TOF), peripheral pulmonary artery stenosis (PPS); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.23 | FGD5 |
Ida Ertmanska gene: FGD5 was added gene: FGD5 was added to Fetal anomalies. Sources: Expert Review Amber,NHS GMS Mode of inheritance for gene: FGD5 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: FGD5 were set to 41574350; 41199744; 30232381; 32037394 Phenotypes for gene: FGD5 were set to Congenital heart disease, tetralogy of Fallout (TOF), peripheral pulmonary artery stenosis (PPS) |
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