congenital nonspherocytic hemolytic anemia
Human disease
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Summary
congenital nonspherocytic hemolytic anemia is a rare disease[1]. It is known by 8 alternative names across languages and contexts.[2]
Key Facts
- Instance of: class of disease[3]
- Subclass of: congenital hemolytic anemia[4], hemolytic anemia due to a disorder of glycolytic enzymes[5], disorder of glycolysis[6]
- Prevalence: 0.000001[7]
- Health specialty: hematology[8], medical genetics[9]
- Genetic association: GPI[10], G6PD[11]
- Age of onset: infantile onset[12], neonatal onset[13]
- Exact match: http://purl.obolibrary.org/obo/DOID_2861[14], http://identifiers.org/doid/DOID:2861[15], http://www.orpha.net/ORDO/Orphanet_712[16]
- On focus list of Wikimedia project: WikiProject Medicine[17]
- Has phenotype: jaundice[18], splenomegaly[19], reticulocytosis[20], Q141815117[21], hepatomegaly[22], unconjugated hyperbilirubinemia[23], cholecystitis[24], disability affecting intellectual abilities[25], hydrops fetalis[26], poikilocytosis[27], Q141816111[28]
- P14914: D00712[29]