Disease: Hemolytic Anemia, Nonspherocytic, Due To Hexokinase Deficiency

Name Hemolytic Anemia, Nonspherocytic, Due To Hexokinase Deficiency

Synonyms -

Classification genetic, haematological

Phenotypes Abnormality of metabolism/homeostasis; Autosomal recessive inheritance; Cholecystitis; Cholelithiasis; Congenital onset; Hyperbilirubinemia; Jaundice; Nonspherocytic hemolytic anemia; Normochromic anemia; Normocytic anemia; Reticulocytosis; Splenomegaly

Associated Genes HK1

Mouse Orthologs Hk1 (Withdrawn symbols: BB404130, Hk-1, dea )

Source OMIM:235700 (names, synonyms, disease associated genes),
Orphanet (disease classes),
HGNC, Ensembl, MGI (gene symbols, gene orthology)
HPO (phenotypes)

Mouse Model: phenotype-based associations

Disease phenotypes are compared with mouse phenotypes, with each mouse model contributing one point to the diagram. Scores are computed according to phenotype specificity and cross-species similarity. X-axis shows the score of the single phenotype that contributes most. Y-axis shows an average among all phenotype matches. The curved line designates a visualization threshold; models below threshold are omitted, except when their genotype matches a disease-associated gene.

Mouse Models

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