Activity
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3 actions
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| Fetal anomalies v8.26 | EIF3A | Ida Ertmanska commented on gene: EIF3A | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.25 | EIF3A | Soo-Mi Park reviewed gene: EIF3A: Rating: AMBER; Mode of pathogenicity: ; Publications: 41033306, 34179316; Phenotypes: syndromic disease, MONDO:0002254, Cardiovascular, craniofacial, and neurodevelopmental disorder; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.23 | EIF3A |
Ida Ertmanska gene: EIF3A was added gene: EIF3A was added to Fetal anomalies. Sources: Expert Review Amber,NHS GMS Mode of inheritance for gene: EIF3A was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: EIF3A were set to 41033306; 34179316 Phenotypes for gene: EIF3A were set to syndromic disease, MONDO:0002254; Cardiovascular, craniofacial, and neurodevelopmental disorder |
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