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| Fetal anomalies v8.26 | NCAPG2 | Ida Ertmanska commented on gene: NCAPG2 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.25 | NCAPG2 | Beth Young reviewed gene: NCAPG2: Rating: AMBER; Mode of pathogenicity: ; Publications: 30609410; Phenotypes: Khan-Khan-Katsanis syndrome, MONDO:0032764, Khan-Khan-Katsanis syndrome, OMIM:618460; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.23 | NCAPG2 |
Ida Ertmanska gene: NCAPG2 was added gene: NCAPG2 was added to Fetal anomalies. Sources: Expert Review Amber,NHS GMS Mode of inheritance for gene: NCAPG2 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: NCAPG2 were set to 30609410 Phenotypes for gene: NCAPG2 were set to Khan-Khan-Katsanis syndrome, MONDO:0032764; Khan-Khan-Katsanis syndrome, OMIM:618460 |
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