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    | Disease #00074 (NPHS1 (nephrotic syndrome, type 1 (NPHS-1, Finnish congenital nephrosis (CNF))), OMIM:256300)
        
          | Official abbreviation | NPHS1 |  
          | Name | nephrotic syndrome, type 1 (NPHS-1, Finnish congenital nephrosis (CNF)) |  
          | OMIM ID | 256300 |  
          | Human Phenotype Ontology Project (HPO) | HPO |  
          | Inheritance | Autosomal recessive |  
          | Individuals reported having this disease | 4 |  
          | Phenotype entries for this disease | 4 |  
          | Associated with 1 gene | NPHS1 |  
          | Associated tissues | - |  
          | Disease features | - |  
          | Remarks | - |  
          | Date created | 2012-11-09 14:39:22 +01:00 (CET) |  
          | Date last edited | 2021-12-10 21:51:32 +01:00 (CET) |  
 
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