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| Fetal anomalies v8.26 | RRP12 | Ida Ertmanska commented on gene: RRP12 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.25 | RRP12 | Soo-Mi Park reviewed gene: RRP12: Rating: AMBER; Mode of pathogenicity: ; Publications: 42144846, 41059649; Phenotypes: basal ganglia calcification, idiopathic, 11, autosomal recessive, MONDO:0980939, Basal ganglia calcification, idiopathic, 11, autosomal recessive, OMIM:621452; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.23 | RRP12 |
Ida Ertmanska gene: RRP12 was added gene: RRP12 was added to Fetal anomalies. Sources: Expert Review Amber,NHS GMS Mode of inheritance for gene: RRP12 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: RRP12 were set to 42144846; 41059649 Phenotypes for gene: RRP12 were set to basal ganglia calcification, idiopathic, 11, autosomal recessive, MONDO:0980939; Basal ganglia calcification, idiopathic, 11, autosomal recessive, OMIM:621452 |
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