Activity
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3 actions
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| Congenital diaphragmatic hernia v0.89 | FOXC2 | Zornitza Stark Marked gene: FOXC2 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital diaphragmatic hernia v0.89 | FOXC2 | Zornitza Stark Gene: foxc2 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital diaphragmatic hernia v0.89 | FOXC2 |
Zornitza Stark gene: FOXC2 was added gene: FOXC2 was added to Congenital diaphragmatic hernia. Sources: Literature Mode of inheritance for gene: FOXC2 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: FOXC2 were set to 33461977; 27663689 Phenotypes for gene: FOXC2 were set to Lymphedema-distichiasis syndrome, MIM# 153400 Review for gene: FOXC2 was set to RED Added comment: Single individual reported with CDH, some supportive functional data. Sources: Literature |
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