Activity
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| Fetal anomalies v8.26 | FHL2 | Ida Ertmanska commented on gene: FHL2 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.25 | FHL2 | Esther Kinning reviewed gene: FHL2: Rating: AMBER; Mode of pathogenicity: ; Publications: 41039806, 36854411, 25358972; Phenotypes: Congential dilated cardiomyopathy, dilated cardiomyopathy, MONDO:0005021; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.23 | FHL2 |
Ida Ertmanska gene: FHL2 was added gene: FHL2 was added to Fetal anomalies. Sources: Expert Review Amber,NHS GMS Mode of inheritance for gene: FHL2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: FHL2 were set to 41039806; 36854411; 25358972 Phenotypes for gene: FHL2 were set to Congential dilated cardiomyopathy; dilated cardiomyopathy, MONDO:0005021 |
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