|   
  
    | Phenotype #0000079446
        
          | Individual ID | 00065273 |  
          | Associated disease | HMLR1 |  
          | Phenotype details | Amelogenesis imperfecta (HP:0000705), no intellectual disability (HP:0001249), bilateral sensorineural hearing loss (HP:0008619), profound sensorineural hearing impairment (HP:0011476), Beau’s lines (-HP:?), onychoschizia (HP:?), retinal pigmentation (HP:0007703), no macular dystrophy (-HP:0007754) |  
          | Diagnosis/Initial | - |  
          | Inheritance | Familial, autosomal recessive |  
          | Diagnosis/Definite | - |  
          | Age/Examination | 21y (21 years) |  
          | Age/Diagnosis | 01y |  
          | Age/Onset | - |  
          | Phenotype/Onset | - |  
          | Protein | - |  
          | Owner name | Jamie Zeegers |  
          | Database submission license | No license selected |  
          | Created by | Johan den Dunnen |  
          | Date created | 2017-03-19 16:32:54 +01:00 (CET) |  
          | Date last edited | N/A |  |  
 
    Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
    Use our APIs  to retrieve data.
 |