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| Fetal anomalies v8.26 | COX18 | Ida Ertmanska commented on gene: COX18 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.25 | COX18 | Esther Kinning reviewed gene: COX18: Rating: AMBER; Mode of pathogenicity: ; Publications: 37468577; Phenotypes: Mitochondrial complex IV deficiency, nuclear type 25, OMIM:621487, neonatal hypertrophic cardiomyopathy, mitochondrial complex IV deficiency, nuclear-type, MONDO:0033885; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.23 | COX18 |
Ida Ertmanska gene: COX18 was added gene: COX18 was added to Fetal anomalies. Sources: Expert Review Amber,NHS GMS Mode of inheritance for gene: COX18 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: COX18 were set to 37468577 Phenotypes for gene: COX18 were set to Mitochondrial complex IV deficiency, nuclear type 25, OMIM:621487; neonatal hypertrophic cardiomyopathy; mitochondrial complex IV deficiency, nuclear-type, MONDO:0033885 |
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