MeSH Treeview
Query OMIM entry list
606938
UROS
UROPORPHYRINOGEN III SYNTHASE
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Neoplasms
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Porphyrias
Porphyria, Erythropoietic
Skin Diseases, Genetic
Porphyria, Erythropoietic
Skin and Connective Tissue Diseases
Skin Diseases
Skin Diseases, Genetic
Porphyria, Erythropoietic
Skin Diseases, Metabolic
Porphyrias
Porphyria, Erythropoietic
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Porphyrias
Porphyria, Erythropoietic
Porphyrias
Porphyria, Erythropoietic
Skin Diseases, Metabolic
Porphyrias
Porphyria, Erythropoietic
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
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