Activity
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3 actions
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| Fetal anomalies v8.26 | FTH1 | Ida Ertmanska commented on gene: FTH1 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.25 | FTH1 | Beth Young reviewed gene: FTH1: Rating: AMBER; Mode of pathogenicity: ; Publications: 37660254, 41551370; Phenotypes: Neurodegeneration with brain iron accumulation-9, OMIM:620669, neurodegeneration with brain iron accumulation 9, MONDO:0958012; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.23 | FTH1 |
Ida Ertmanska gene: FTH1 was added gene: FTH1 was added to Fetal anomalies. Sources: Expert Review Amber,NHS GMS Mode of inheritance for gene: FTH1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: FTH1 were set to 37660254; 41551370 Phenotypes for gene: FTH1 were set to Neurodegeneration with brain iron accumulation-9, OMIM:620669; neurodegeneration with brain iron accumulation 9, MONDO:0958012 |
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