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Tyrosinemia: A rare genetic metabolic disorder characterized by lack of the enzyme fumarylacetoacetate hydrolase (FAH) - which is needed to break down the amino acid tyrosine. Conditions and Diseases Rare Disorders Tyrosinemia:  English Health Conditions and Diseases: Genetic Disorders English Health Conditions and Diseases: Nutrition and Metabolism Disorders Gene ClinicsHealth: Gene, Rare Disorders Tyrosinemia · Medical genetics knowledge base Clinics NIH funded, expert-authored descriptions of inherited disorders. Covers genetic testing in diagnosis and management and genetic counseling of patients. National Library of MedicineHealth: National, Rare Disorders Tyrosinemia The synonyms of Tyrosinemia 11 Library of Medicine a summary and major features. TyrosinemiaHealth: Tyrosinemia, Rare Disorders Tyrosinemia For all people interested in connecting with others with this disease Tyrosinemia . NORD: Tyrosinemia, HereditaryHealth: NORD, Rare Disorders Tyrosinemia Offers the synonyms Tyrosinemia, Hereditary a general discussion and further resources. Primary Ciliary Dyskinesia - TyrosinemiaHealth: Primary, Rare Disorders Tyrosinemia · Information on a rare congenital disease Ciliary Dyskinesia Tyrosinemia . Medical FoodsHealth: Medical, Rare Disorders Tyrosinemia · FDA/CFSAN Office of Special Nutritionals: Explaniation as to what these are Foods how the FDA over sees them and how to get more information. Mucopolysaccharidoses - TyrosinemiaHealth: Mucopolysaccharidoses, Rare Disorders Tyrosinemia · Information sheet compiled by the National Institute of Neurological Disorders and Stroke Tyrosinemia NINDS,. Office of Rare DiseasesConditions and Diseases Rare Disorders - Information on more than 6000 rare diseases of Rare Diseases including current research, publications from scientific and medical journals, completed research, ongoing studies, and patient support groups. Lymphangiomatosis and Gorham's Vanishing Bone DiseaseConditions and Diseases Rare Disorders - Provides general information and a personal account and Gorham's Vanishing Bone Disease including pictures and X-rays. Also offers patient contact and an email discussion group. CherubsConditions and Diseases Rare Disorders - A non-profit support group for the families and medical care providers of children and adults born with Congenital Diaphragmatic Hernia Cherubs . Nomid /Cinca - TyrosinemiaConditions and Diseases Rare Disorders - Resource for parents and patients suffering from Neonatal Onset Multi-inflammatory Disease Chronic /Cinca Tyrosinemia or Infantile, Neurologic, Cutaneous and Articular syndrome. Site maintained by patients, parents and friends for their counterparts worldwide. Email support group at eGroups. Fibrous Dysplasia Support Online - TyrosinemiaConditions and Diseases Rare Disorders - For those seeking support and information concerning the rare bone diseases: fibrous dysplasia Dysplasia Support Online Tyrosinemia McCune Albright Syndrome and Cherubism. | |||||||