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    | Disease #05834 (EL3 (elliptocytosis, type 3 (EL3, anemia, neonatal hemolytic, fatal or near-fatal)), OMIM:617948)
        
          | Official abbreviation | EL3 |  
          | Name | elliptocytosis, type 3 (EL3, anemia, neonatal hemolytic, fatal or near-fatal) |  
          | OMIM ID | 617948 |  
          | Human Phenotype Ontology Project (HPO) | HPO |  
          | Inheritance | - |  
          | Individuals reported having this disease | - |  
          | Phenotype entries for this disease | - |  
          | Associated with 1 gene | SPTB |  
          | Associated tissues | - |  
          | Disease features | - |  
          | Remarks | - |  
          | Date created | 2020-09-15 10:18:09 +02:00 (CEST) |  
          | Date last edited | N/A |  |  
 
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