RS80338901 FAH
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What This Variant Does
"Two novel mutations involved in hereditary tyrosinemia type I. A single mutation of the fumarylaceto...
Associated Conditions
Tyrosinemia type I
FAH-related disorder
Inborn genetic diseases
Tyrosinemia
Ovarian serous cystadenocarcinoma
Thymoma
Tyrosinemia type I
FAH-related disorder
Inborn genetic diseases
Tyrosinemia
Ovarian serous cystadenocarcinoma
Thymoma
Other Variants in FAH