Search Ontology:
Human Disease

congenital nonspherocytic hemolytic anemia 5

Term ID
DOID:0051006
Synonyms
Definition
A congenital nonspherocytic hemolytic anemia that has_material_basis_in homozygous or compound heterozygous mutation in the HK1 gene, which encodes a form of hexokinase, on chromosome 10q22. https://pubmed.ncbi.nlm.nih.gov/12393545/
References
Ontology
Human Disease   ( DOID:0051006 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models
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