Activity
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3 actions
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| Fetal anomalies v8.26 | MYCBP2 | Ida Ertmanska commented on gene: MYCBP2 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.25 | MYCBP2 | Alice Gardham reviewed gene: MYCBP2: Rating: GREEN; Mode of pathogenicity: ; Publications: 41543631, 36200388, 41200582; Phenotypes: neurodevelopmental disorder, MONDO:0700092; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.23 | MYCBP2 |
Ida Ertmanska gene: MYCBP2 was added gene: MYCBP2 was added to Fetal anomalies. Sources: Expert Review Amber,NHS GMS Mode of inheritance for gene: MYCBP2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: MYCBP2 were set to 41543631; 36200388; 41200582 Phenotypes for gene: MYCBP2 were set to neurodevelopmental disorder, MONDO:0700092 |
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