Legend:

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

'Brain Diseases, Metabolic, Inborn'  (Integration tree)

Pathogenesis

• Genetic disorders of glycan degradation

Disorders by systems

• Genetic disorders of glycan degradation (by systems, signs and symptoms)
  • Diseases
    • Nervous System Diseases
      • Central Nervous System Diseases
        • Brain Diseases
          • Brain Diseases, Metabolic
            • Brain Diseases, Metabolic, Inborn
              • Aspartylglucosaminuria (GDGDB) [AGA]
              • Fucosidosis (GDGDB) [FUCA1]
              • Sialidosis (GDGDB) [NEU1]
              • Mucolipidosis II (alpha/beta) (GDGDB) [GNPTAB]
              • Mucolipidosis III (alpha/beta) (GDGDB) [GNPTAB]
              • GM1-gangliosidosis, type I (GDGDB) [GLB1]
              • GM1-gangliosidosis, type II (GDGDB) [GLB1]
              • GM1-gangliosidosis, type III (GDGDB) [GLB1]
              • Tay-Sachs disease (GDGDB) [HEXA]
              • Sandhoff disease (GDGDB) [HEXB]
              • GM2-gangliosidosis, AB variant (GDGDB) [GM2A]
              • Fabry disease (GDGDB) [GLA]
              • Gaucher disease, type II (GDGDB) [GBA]
              • Gaucher disease, type III (GDGDB) [GBA]
              • Gaucher disease, atypical, due to saposin C deficiency (GDGDB) [PSAP]
              • Krabbe disease (GDGDB) [GALC]
              • Multiple sulfatase deficiency (GDGDB) [SUMF1]
              • Metachromatic leukodystrophy (GDGDB) [ARSA]
              • Metachromatic leukodystrophy, due to saposin B deficiency (GDGDB) [PSAP]
              • Niemann-Pick disease, type A (GDGDB) [SMPD1]
              • Niemann-Pick disease, type C1 (GDGDB) [NPC1]
              • Niemann-Pick disease, type C2 (GDGDB) [NPC2]
              • Farber Lipogranulomatosis (GDGDB) [ASAH1]