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| Pigmentary skin disorders v0.27 | FANCB |
Catherine Snow Added phenotypes FANCB; FANCONI ANEMIA, COMPLEMENTATION GROUP B for gene: FANCB Publications for gene FANCB were changed from to 15502827 |
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| Pigmentary skin disorders v0.25 | FANCB | Tom Cullup reviewed gene: FANCB: Rating: GREEN; Mode of pathogenicity: ; Publications: 15502827; Phenotypes: FANCONI ANEMIA, COMPLEMENTATION GROUP B, FANCB; Mode of inheritance: X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Pigmentary skin disorders v0.23 | FANCB |
Catherine Snow Source Expert Review Green was added to FANCB. Rating Changed from Red List (low evidence) to Green List (high evidence) |
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| Pigmentary skin disorders v0.22 | FANCB | Catherine Snow reviewed gene: FANCB: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Pigmentary skin disorders v0.21 | FANCB |
Catherine Snow gene: FANCB was added gene: FANCB was added to Pigmentary skin disorders. Sources: Expert Review Mode of inheritance for gene: FANCB was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) |
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