Xanthinuria Type 1
What's New
Last Posted: Mar 06, 2023
- Thiopurine-induced toxicity is associated with dysfunction variant of the human molybdenum cofactor sulfurase gene (xanthinuria type II).
Stiburkova Blanka, et al. Toxicology and applied pharmacology 2018 0 102-108 - Hereditary xanthinuria is not so rare disorder of purine metabolism.
Sebesta I et al. Nucleosides, nucleotides & nucleic acids 2018 37(6) 324-328 - Xanthinuria type 1
From NCATS Genetic and Rare Diseases Information Center - Xanthinuria type 2
From NCATS Genetic and Rare Diseases Information Center
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
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- Page last reviewed:Feb 1, 2024
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