| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Fetal anomalies v0.4673 | PHC1 | Zornitza Stark Marked gene: PHC1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v0.4673 | PHC1 | Zornitza Stark Gene: phc1 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v0.4673 | PHC1 | Zornitza Stark Classified gene: PHC1 as Red List (low evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v0.4673 | PHC1 | Zornitza Stark Gene: phc1 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v0.4546 | PHC1 |
Belinda Chong gene: PHC1 was added gene: PHC1 was added to Fetal anomalies. Sources: Literature Mode of inheritance for gene: PHC1 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: PHC1 were set to 23418308 Phenotypes for gene: PHC1 were set to Microcephaly 11, primary, autosomal recessive, MIM#615414 Review for gene: PHC1 was set to RED gene: PHC1 was marked as current diagnostic Added comment: Short stature and microcephaly, currently not enough information. Single family reported with functional data. Sources: Literature |
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