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    | Disease #01820 (GSD1B (glycogen storage disease, type Ib (GSD1B)), OMIM:232220)
        
          | Official abbreviation | GSD1B |  
          | Name | glycogen storage disease, type Ib (GSD1B) |  
          | OMIM ID | 232220 |  
          | Human Phenotype Ontology Project (HPO) | HPO |  
          | Inheritance | Autosomal recessive |  
          | Individuals reported having this disease | 37 |  
          | Phenotype entries for this disease | 2 |  
          | Associated with 1 gene | SLC37A4 |  
          | Associated tissues | - |  
          | Disease features | - |  
          | Remarks | - |  
          | Date created | 2014-09-25 23:29:40 +02:00 (CEST) |  
          | Date last edited | 2021-02-03 14:20:19 +01:00 (CET) |  
 
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