| Disease Aliases (36) | Ank1 hereditary spherocytosis Ank1-related hereditary spherocytosis Ank1-related spherocytosis Acholuric (familial) jaundice Acholuric jaundice Chronic acholuric jaundice Congenital (spherocytic) hemolytic icterus Congenital spherocytic hemolytic anemia Congenital spherocytosis Congenital hemolytic jaundice Debrie's familial haemolytic disease Familial acholuric jaundice Familial spherocytosis Hs Hs - hereditary spherocytosis Hs1 Hereditary spherocytoses Minkowski chauffard syndrome Minkowski-chauffard disease Minkowski-chauffard haemolytic jaundice Minkowski-chauffard syndrome Minkowski-chauffard-gã¤nsslen syndrome Minkowski-chauffard-gänsslen syndrome Minkowsky-chauffard syndrome Sph1 Spherocytosis, hereditary, 1 Spherocytic anemia Spherocytoses, hereditary Spherocytosis, hereditary Hereditary spherocytosis 1 Hereditary spherocytosis caused by mutation in ank1 Hereditary spherocytosis type 1 Spherocytosis, type 1 Spherocytosis, type 1; sph1 |
Associated Genes (5) NCBI-RefSeq: ANK1 (Ankyrin 1) External Links: gnomAD browser Ensembl GeneCards
NCBI-RefSeq: EPB42 (Erythrocyte membrane protein band 4.2) External Links: gnomAD browser Ensembl GeneCards
NCBI-RefSeq: SLC4A1 (Solute carrier family 4 member 1 (Diego blood group)) External Links: gnomAD browser Ensembl GeneCards
NCBI-RefSeq: SPTB (Spectrin beta, erythrocytic) External Links: gnomAD browser Ensembl GeneCards
NCBI-RefSeq: SPTA1 (Spectrin alpha, erythrocytic 1) External Links: gnomAD browser Ensembl GeneCards
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| Cross-references of Hereditary spherocytosis | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |