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Disease Anemia, Nonspherocytic Hemolytic, possibly due to Defect in Porphyrin Metabolism

Name Anemia, Nonspherocytic Hemolytic, possibly due to Defect in Porphyrin Metabolism
Categories Blood disease | Genetic disease (inborn)
MeSH® ID C565952

Top ↑ Ancestors

1. DiseasesHemic and Lymphatic Diseases Has associated chemicals Has associated genes Has associated exposure references Hematologic Diseases Has associated chemicals Has associated genes Has associated exposure references Anemia Has associated chemicals Has associated genes Has associated exposure references Anemia, Hemolytic Has associated chemicals Has associated genes Has associated exposure references Anemia, Hemolytic, Congenital Has associated chemicals Has associated genes Has associated exposure references Anemia, Hemolytic, Congenital Nonspherocytic Has associated chemicals Has associated genes Anemia, Nonspherocytic Hemolytic, possibly due to Defect in Porphyrin Metabolism
2. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated exposure references Anemia, Hemolytic, Congenital Has associated chemicals Has associated genes Has associated exposure references Anemia, Hemolytic, Congenital Nonspherocytic Has associated chemicals Has associated genes Anemia, Nonspherocytic Hemolytic, possibly due to Defect in Porphyrin Metabolism

Top ↑ Descendants

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