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| Fetal anomalies v8.26 | UBR5 | Ida Ertmanska commented on gene: UBR5 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.25 | UBR5 | Natalie Chandler reviewed gene: UBR5: Rating: AMBER; Mode of pathogenicity: ; Publications: 39721588; Phenotypes: Neurodevelopmental disorder with speech delay and behavioral abnormalities, OMIM:621372; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.23 | UBR5 |
Ida Ertmanska gene: UBR5 was added gene: UBR5 was added to Fetal anomalies. Sources: Expert Review Amber,NHS GMS Mode of inheritance for gene: UBR5 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: UBR5 were set to 39721588 Phenotypes for gene: UBR5 were set to Neurodevelopmental disorder with speech delay and behavioral abnormalities, OMIM:621372 |
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