Inherited Metabolic Diseases / NEWBORN SCREENING FACT SHEET FAH Deficiency / Seizures / liver failure / Coma / amino acid disorder / Fumarylacetoacetase deficiency / numbness / tyrosinemia / diarrhea / Rickets / severe liver disease / Allied Disorders / chronic form / neurologic symptoms / FAH Diarrhea / Hepatorenal tyrosinemia / tyrosinemia type III / Hereditary / cancer / Fumarylacetoacetate hydrolace deficiency / nodular cirrhosis / fever / vomiting / pain / infantile tyrosinemia / liver cancer / tyrosinemia type II / high blood pressure / /
MedicalTreatment
liver transplant / /
Organization
FAH National Urea Cycle Disorders Foundation / University of North Dakota School of Medicine / North Dakota Department of Health Newborn Screening Program / Coalition for PKU / ND Pathfinder Family Center / Family Network Center / Department of Health / / /