| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Skeletal dysplasia v1.0 | MANBA | Gene migrated from ENSG00000109323 to ENSG00000109323 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Skeletal dysplasia v0.0 | MANBA |
Zornitza Stark gene: MANBA was added gene: MANBA was added to Skeletal dysplasia. Sources: NHS GMS,Expert Review Amber Mode of inheritance for gene: MANBA was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: MANBA were set to 18980795; 16401745; 2079835 Phenotypes for gene: MANBA were set to Beta-mannosidosis, 248510 |
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