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Ectodermal dysplasia v0.26 | DHX40 | Catherine Snow Classified gene: DHX40 as Red List (low evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Ectodermal dysplasia v0.26 | DHX40 | Catherine Snow Added comment: Comment on list classification: Currently no gene disease association can be found. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Ectodermal dysplasia v0.26 | DHX40 | Catherine Snow Gene: dhx40 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Ectodermal dysplasia v0.22 | DHX40 | Catherine Snow Phenotypes for gene: DHX40 were changed from Corneal dystrophy, posterior polymorphous, 4, 618031; Deafness, autosomal dominant 28, 608641; Ectodermal dysplasia/short stature syndrome, 616029 to Ectodermal dysplasia | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Ectodermal dysplasia v0.19 | DHX40 | Catherine Snow Phenotypes for gene: DHX40 were changed from to Corneal dystrophy, posterior polymorphous, 4, 618031; Deafness, autosomal dominant 28, 608641; Ectodermal dysplasia/short stature syndrome, 616029 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Ectodermal dysplasia v0.18 | DHX40 | Catherine Snow reviewed gene: DHX40: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Ectodermal dysplasia v0.15 | DHX40 |
Catherine Snow gene: DHX40 was added gene: DHX40 was added to Ectodermal dysplasia. Sources: Expert Review Amber Mode of inheritance for gene: DHX40 was set to |