| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Hydrops fetalis v0.175 | CLCNKB | Zornitza Stark Publications for gene: CLCNKB were set to | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hydrops fetalis v0.174 | CLCNKB |
Zornitza Stark changed review comment from: Typically Bartter syndrome presents with polyhydramnios antenatally, cannot find specific reference though OMIM lists hydrops as a feature. Sources: Expert list; to: Typically Bartter syndrome presents with polyhydramnios antenatally, single case report of hydrops identified. Sources: Expert list |
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| Hydrops fetalis v0.174 | CLCNKB | Zornitza Stark edited their review of gene: CLCNKB: Changed publications: 23484775 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hydrops fetalis v0.14 | CLCNKB | Zornitza Stark Marked gene: CLCNKB as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hydrops fetalis v0.14 | CLCNKB | Zornitza Stark Gene: clcnkb has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Hydrops fetalis v0.14 | CLCNKB |
Zornitza Stark gene: CLCNKB was added gene: CLCNKB was added to Hydrops fetalis_VCGS. Sources: Expert list Mode of inheritance for gene: CLCNKB was set to Other Phenotypes for gene: CLCNKB were set to Bartter syndrome, type 4b, digenic, MIM#613090 Review for gene: CLCNKB was set to RED Added comment: Typically Bartter syndrome presents with polyhydramnios antenatally, cannot find specific reference though OMIM lists hydrops as a feature. Sources: Expert list |
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