Legend:

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

'Gaucher disease'  (Integration tree)

Pathogenesis

• Genetic disorders of glycan degradation
  • Disorders of sphingolipid metabolism and other lipid storage disorders
    • Sphingolipidosis
      • Other sphingolipidosis
        • Gaucher disease
          • Gaucher disease, type I (GDGDB) [GBA]
          • Gaucher disease, type II (GDGDB) [GBA]
            • Gaucher disease, type II, neuronopathic form, classic type [GBA]
            • Gaucher disease, type II, perinatal lethal form [GBA]
          • Gaucher disease, type III (GDGDB) [GBA]
          • Gaucher disease, type IIIC (GDGDB) [GBA]
          • Gaucher disease, atypical, due to saposin C deficiency (GDGDB) [PSAP]

Disorders by systems

• Genetic disorders of glycan degradation (by systems, signs and symptoms)