|   
  
    | Phenotype #0000199679
        
          | Individual ID | 00261173 |  
          | Associated disease | DD |  
          | Phenotype details | developmental delay/intellectual disability (HP:0012758/HP:0001249); autism spectrum disorder (HP:0000729); attention deficit hyperactivity disorder (HP:0007018); no stereotypic behavior (-HP:0000733); no seizures (-HP:0001250); muscular hypotonia (HP:0001252); no ataxia (-HP:0001251); no abnormal prenatal brain imaging; microcephaly (HP:0000252); no macrocephaly (-HP:0000256); facial dysmorphism (HP:0000271);  small joint hypermobility |  
          | Diagnosis/Initial | developmental delay |  
          | Inheritance | Isolated (sporadic) |  
          | Diagnosis/Definite | - |  
          | Age/Examination | 9y (9 years) |  
          | Age/Diagnosis | - |  
          | Age/Onset | - |  
          | Phenotype/Onset | - |  
          | Protein | - |  
          | Owner name | Johan den Dunnen |  
          | Database submission license | Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International   |  
          | Created by | Johan den Dunnen |  
          | Date created | 2019-08-11 12:19:47 +02:00 (CEST) |  
          | Date last edited | N/A |  |  
 
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