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| Ectodermal Dysplasia v1.0 | MSX1 | Gene migrated from ENSG00000163132 to ENSG00000163132 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Ectodermal Dysplasia v0.103 | chirag patel Added reviews for gene MSX1 from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Ectodermal Dysplasia v0.0 | MSX1 |
Bryony Thompson gene: MSX1 was added gene: MSX1 was added to Ectodermal Dysplasia_RMH. Sources: Royal Melbourne Hospital,Expert Review Green Mode of inheritance for gene: MSX1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: MSX1 were set to Ectodermal dysplasia 3, Witkop type, 189500 |
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