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Severe Paediatric Disorders v0.12 WNT7A Louise Daugherty reviewed gene: WNT7A: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 WNT7A Louise Daugherty Publications for gene WNT7A were updated from to 30847515
Severe Paediatric Disorders v0.10 WNT7A Louise Daugherty Added phenotypes Ulna and fibula, absence of, with severe limb deficiency, 276820; Fuhrmann syndrome, 228930 for gene: WNT7A
Severe Paediatric Disorders v0.9 WNT7A Louise Daugherty Added phenotypes Ulna and fibula, absence of, with severe limb deficiency, 276820; Fuhrmann syndrome, 228930 for gene: WNT7A
Severe Paediatric Disorders v0.9 WNT7A Louise Daugherty Added phenotypes Ulna and fibula, absence of, with severe limb deficiency, 276820; Fuhrmann syndrome, 228930 for gene: WNT7A
Severe Paediatric Disorders v0.8 WNT7A Louise Daugherty Added phenotypes Ulna and fibula, absence of, with severe limb deficiency, 276820; Fuhrmann syndrome, 228930 for gene: WNT7A
Severe Paediatric Disorders v0.8 WNT7A Louise Daugherty Mode of inheritance for gene WNT7A was changed from to BIALLELIC, autosomal or pseudoautosomal
Added phenotypes Ulna and fibula, absence of, with severe limb deficiency, 276820; Fuhrmann syndrome, 228930 for gene: WNT7A
Severe Paediatric Disorders v0.7 WNT7A Louise Daugherty Source Next Generation Children Project was added to WNT7A.
Severe Paediatric Disorders v0.5 WNT7A Louise Daugherty Source Expert Review Green was added to WNT7A.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 WNT7A Louise Daugherty gene: WNT7A was added
gene: WNT7A was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: WNT7A was set to