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| Mendeliome v1.4413 | BMS1 | Bryony Thompson Marked gene: BMS1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mendeliome v1.4413 | BMS1 | Bryony Thompson Gene: bms1 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mendeliome v1.4413 | BMS1 |
Bryony Thompson gene: BMS1 was added gene: BMS1 was added to Mendeliome. Sources: Literature Mode of inheritance for gene: BMS1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: BMS1 were set to 23785305 Phenotypes for gene: BMS1 were set to aplasia cutis congenita MONDO:0007145 Review for gene: BMS1 was set to RED Added comment: A single family reported. Sources: Literature |
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