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General Information
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| Term |
congenital dyserythropoietic anemia type IVb |
ID (Ontology) |
DOID:0051002 (Human Disease) |
| Definition |
A congenital dyserythropoietic anemia characterized by neonatal jaundice, hyperbilirubinemia, and severe congenital hemolytic anemia requiring transfusionn and that has_material_basis_in homozygous or compound heterozygous mutation in the KLF1 gene on chromosome 19p13.13. |
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Links to External Ontologies
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DO.org
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Annotations
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Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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No relevant records available
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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| Full annotation statements | Relevant FlyBase reports |
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| Genes |
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congenital dyserythropoietic anemia type IVb | 2 | for disease ribbon | congenital dyserythropoietic anemia type IVb | 2 | model of | congenital dyserythropoietic anemia type IVb | 2 |
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