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| Congenital diaphragmatic hernia v0.86 | BRCA2 | Zornitza Stark Marked gene: BRCA2 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital diaphragmatic hernia v0.86 | BRCA2 | Zornitza Stark Gene: brca2 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital diaphragmatic hernia v0.86 | BRCA2 |
Zornitza Stark gene: BRCA2 was added gene: BRCA2 was added to Congenital diaphragmatic hernia. Sources: Literature Mode of inheritance for gene: BRCA2 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: BRCA2 were set to Fanconi anemia, complementation group D1, MIM# 605724 Review for gene: BRCA2 was set to RED Added comment: Single affected individual reported, although FA is a multiple congenital anomaly syndrome. Sources: Literature |
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