Details of Disease

General Information of Disease (ID: DIS840H2)

• Disease Name: Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome
• Disease Hierarchy:
  DIS6SVEE: Syndromic disease
  DISYKSRF: Genetic disease
  DIS840H2: Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome