Activity
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| Fetal anomalies v8.26 | KLHL20 | Ida Ertmanska commented on gene: KLHL20 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.25 | KLHL20 | Anna de Burca reviewed gene: KLHL20: Rating: RED; Mode of pathogenicity: ; Publications: 36214804, 38513146; Phenotypes: neurodevelopmental disorder with early-onset seizures, facial dysmorphism, and behavioral abnormalities, MONDO:0980709, Neurodevelopmental disorder with early-onset seizures, facial dysmorphism, and behavioral abnormalities, OMIM:621390; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.23 | KLHL20 |
Ida Ertmanska gene: KLHL20 was added gene: KLHL20 was added to Fetal anomalies. Sources: NHS GMS,Expert Review Red Mode of inheritance for gene: KLHL20 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: KLHL20 were set to 36214804; 38513146 Phenotypes for gene: KLHL20 were set to neurodevelopmental disorder with early-onset seizures, facial dysmorphism, and behavioral abnormalities, MONDO:0980709; Neurodevelopmental disorder with early-onset seizures, facial dysmorphism, and behavioral abnormalities, OMIM:621390 |
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