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| Fetal anomalies v8.26 | DMRT2 | Ida Ertmanska commented on gene: DMRT2 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.25 | DMRT2 | Sarah Graham reviewed gene: DMRT2: Rating: GREEN; Mode of pathogenicity: ; Publications: 29681102, 41014130, 16387292; Phenotypes: spondylocostal dysostosis 7, autosomal recessive, MONDO:0981023, Spondylocostal dysostosis 7, autosomal recessive, OMIM:621523; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.23 | DMRT2 |
Ida Ertmanska gene: DMRT2 was added gene: DMRT2 was added to Fetal anomalies. Sources: Expert Review Amber,NHS GMS Mode of inheritance for gene: DMRT2 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: DMRT2 were set to 29681102; 41014130; 16387292 Phenotypes for gene: DMRT2 were set to spondylocostal dysostosis 7, autosomal recessive, MONDO:0981023; Spondylocostal dysostosis 7, autosomal recessive, OMIM:621523 |
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