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Desmosomal disorders v1.4 WNT10A Zornitza Stark Marked gene: WNT10A as ready
Desmosomal disorders v1.4 WNT10A Zornitza Stark Gene: wnt10a has been classified as Red List (Low Evidence).
Desmosomal disorders v1.4 WNT10A Zornitza Stark Phenotypes for gene: WNT10A were changed from to Odontoonychodermal dysplasia 257980 AR Schopf-Schulz-Passarge syndrome 224750 AR Tooth agenesis, selective, 4 150400 AR, AD
Desmosomal disorders v1.3 WNT10A Zornitza Stark Mode of inheritance for gene: WNT10A was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Desmosomal disorders v1.2 WNT10A Zornitza Stark Publications for gene: WNT10A were set to
Desmosomal disorders v1.1 WNT10A Zornitza Stark Classified gene: WNT10A as Red List (low evidence)
Desmosomal disorders v1.1 WNT10A Zornitza Stark Gene: wnt10a has been classified as Red List (Low Evidence).
Desmosomal disorders v1.0 WNT10A Zornitza Stark reviewed gene: WNT10A: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
Desmosomal disorders v0.0 WNT10A Zornitza Stark gene: WNT10A was added
gene: WNT10A was added to Desmosomal disorders_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: WNT10A was set to Unknown