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| Congenital hypothyroidism v0.21 | TTF2 | Zornitza Stark Marked gene: TTF2 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital hypothyroidism v0.21 | TTF2 | Zornitza Stark Gene: ttf2 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital hypothyroidism v0.19 | TTF2 |
Chirag Patel gene: TTF2 was added gene: TTF2 was added to Congenital hypothyroidism. Sources: Literature Mode of inheritance for gene: TTF2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: TTF2 were set to PMID: 30022773 Phenotypes for gene: TTF2 were set to congenital hypothyroidism, thyroid dysgenesis, No OMIM # Review for gene: TTF2 was set to RED Added comment: 1 case only Sources: Literature |
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