Search Ontology:
Human Disease

congenital nonspherocytic hemolytic anemia 4

Term ID
DOID:0051005
Synonyms
Definition
A congenital nonspherocytic hemolytic anemia that has_material_basis_in homozygous or compound heterozygous mutation in the PHI gene (GPI) on chromosome 19q13. https://pubmed.ncbi.nlm.nih.gov/8218542/
References
Ontology
Human Disease   ( DOID:0051005 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models
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