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| Hydrops fetalis v0.142 | MID1 | Zornitza Stark Marked gene: MID1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hydrops fetalis v0.142 | MID1 | Zornitza Stark Gene: mid1 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hydrops fetalis v0.142 | MID1 |
Zornitza Stark gene: MID1 was added gene: MID1 was added to Hydrops fetalis. Sources: Expert list Mode of inheritance for gene: MID1 was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females Publications for gene: MID1 were set to 3517843; 24863803 Phenotypes for gene: MID1 were set to Opitz GBBB syndrome, type I 300000 Review for gene: MID1 was set to RED Added comment: Two reports of hydrops in Opitz G, in the context of complex congenital heart disease, one of them dating back to 1986, not molecularly confirmed. Sources: Expert list |
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