| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Congenital hypothyroidism v0.21 | TTF1 | Zornitza Stark Marked gene: TTF1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital hypothyroidism v0.21 | TTF1 | Zornitza Stark Added comment: Comment when marking as ready: Targeted sequencing panel study. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital hypothyroidism v0.21 | TTF1 | Zornitza Stark Gene: ttf1 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital hypothyroidism v0.12 | TTF1 | Chirag Patel Classified gene: TTF1 as Amber List (moderate evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital hypothyroidism v0.12 | TTF1 | Chirag Patel Gene: ttf1 has been classified as Amber List (Moderate Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital hypothyroidism v0.11 | TTF1 |
Chirag Patel gene: TTF1 was added gene: TTF1 was added to Congenital hypothyroidism. Sources: Literature Mode of inheritance for gene: TTF1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: TTF1 were set to PMID: 30022773 Phenotypes for gene: TTF1 were set to congenital hypothyroidism, thyroid dysgenesis, No OMIM # Review for gene: TTF1 was set to AMBER Added comment: 5 cases, but one paper with limited additional evidence Sources: Literature |
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