Legend:

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

'Developmental Disabilities'  (Integration tree)

Pathogenesis

• Genetic disorders of glycan degradation

Disorders by systems

• Genetic disorders of glycan degradation (by systems, signs and symptoms)
  • Psychiatry and Psychology
    • Mental Disorders
      • Mental Disorders Diagnosed in Childhood
        • Developmental Disabilities
          • Aspartylglucosaminuria (GDGDB) [AGA]
          • Schindler disease, type I (GDGDB) [NAGA]
          • Mucolipidosis II (alpha/beta) (GDGDB) [GNPTAB]
          • Hurler syndrome (GDGDB) [IDUA]
          • Hurler-Scheie syndrome (GDGDB) [IDUA]
          • Mucopolysaccharidosis II (GDGDB) [IDS]
          • Sanfilippo syndrome A (GDGDB) [SGSH]
          • Sanfilippo syndrome B (GDGDB) [NAGLU]
          • Sanfilippo syndrome C (GDGDB) [HGSNAT]
          • Sanfilippo syndrome D (GDGDB) [GNS]
          • Mucopolysaccharidosis VII (GDGDB) [GUSB]
          • 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]
          • Gaucher disease, type II (GDGDB) [GBA]
          • Krabbe disease (GDGDB) [GALC]
            • Krabbe disease, infantile form [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]
          • Wolman disease (GDGDB) [LIPA]