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    | Disease #07142 (NEDHBA (neurodevelopmental disorder with hypotonia and characteristic brain abnormalities), OMIM:620746)
        
          | Official abbreviation | NEDHBA |  
          | Name | neurodevelopmental disorder with hypotonia and characteristic brain abnormalities |  
          | OMIM ID | 620746 |  
          | Human Phenotype Ontology Project (HPO) | HPO |  
          | Inheritance | Autosomal recessive |  
          | Individuals reported having this disease | - |  
          | Phenotype entries for this disease | - |  
          | Associated with 1 gene | SLC4A10 |  
          | Associated tissues | - |  
          | Disease features | - |  
          | Remarks | - |  
          | Date created | 2024-12-18 15:46:43 +01:00 (CET) |  
          | Date last edited | N/A |  |  
 
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