Disease #07199 (EL (elliptocytosis))

Official abbreviation EL
Name elliptocytosis
OMIM ID -
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene SPTB
Associated tissues -
Disease features -
Remarks -
Date created 2025-11-17 21:41:39 +01:00 (CET)
Date last edited N/A


Individuals

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00469542 family Journal: Cao 2025 2-generation family, affected daughter/mother F - China - - - - - EL see paper; ..., hereditary spherocytosis, neonatal hemolytic anemia; mother hereditary spherocytosis, hemolytic anemia SPTB SPTB 1 2 Johan den Dunnen
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