Legend:

• Concept Types
  • target (single disease)
  • classification term
  • pathway-based classification term
  • clinical findings
  • multiple types disease
  • single disease
  • disease type

'Gaucher disease, atypical, due to saposin C deficiency'  (Integration tree)

Pathogenesis

• Genetic disorders of glycan degradation
  • Disorders of sphingolipid metabolism and other lipid storage disorders
    • Sphingolipidosis
      • Other sphingolipidosis
        • Gaucher disease
          • Gaucher disease, atypical, due to saposin C deficiency (GDGDB) [PSAP]

Disorders by systems

• Genetic disorders of glycan degradation (by systems, signs and symptoms)
  • Diseases
    • Digestive System Diseases
      • Liver Diseases
        • Hepatomegaly
          • Gaucher disease, atypical, due to saposin C deficiency (GDGDB) [PSAP]
    • Hemic and Lymphatic Diseases
      • Lymphatic Diseases
        • Splenic Diseases
          • Gaucher disease, atypical, due to saposin C deficiency (GDGDB) [PSAP]
    • Nervous System Diseases
      • Central Nervous System Diseases
        • Brain Diseases
          • Brain Diseases, Metabolic
            • Brain Diseases, Metabolic, Inborn
              • Gaucher disease, atypical, due to saposin C deficiency (GDGDB) [PSAP]
      • Neurologic Manifestations
        • Neurobehavioral Manifestations
          • Intellectual Disability
            • Gaucher disease, atypical, due to saposin C deficiency (GDGDB) [PSAP]
  • Psychiatry and Psychology
    • Mental Disorders
      • Mental Disorders Diagnosed in Childhood
        • Intellectual Disability
          • Gaucher disease, atypical, due to saposin C deficiency (GDGDB) [PSAP]