Legend:

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

'Learning Disorders'  (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
      • Neurologic Manifestations
        • Neurobehavioral Manifestations
          • Communication Disorders
            • Learning Disorders
              • Aspartylglucosaminuria (GDGDB) [AGA]
              • Alpha-mannosidosis (GDGDB) [MAN2B1]
              • Schindler disease, type I (GDGDB) [NAGA]
              • Mucolipidosis III (alpha/beta) (GDGDB) [GNPTAB]
              • Hurler syndrome (GDGDB) [IDUA]
              • Hurler-Scheie syndrome (GDGDB) [IDUA]
              • Sanfilippo syndrome A (GDGDB) [SGSH]
              • Sanfilippo syndrome B (GDGDB) [NAGLU]
              • Sanfilippo syndrome C (GDGDB) [HGSNAT]
              • Sanfilippo syndrome D (GDGDB) [GNS]
              • 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]
  • Psychiatry and Psychology
    • Mental Disorders
      • Mental Disorders Diagnosed in Childhood
        • Learning Disorders
          • Aspartylglucosaminuria (GDGDB) [AGA]
          • Alpha-mannosidosis (GDGDB) [MAN2B1]
          • Schindler disease, type I (GDGDB) [NAGA]
          • Mucolipidosis III (alpha/beta) (GDGDB) [GNPTAB]
          • Hurler syndrome (GDGDB) [IDUA]
          • Hurler-Scheie syndrome (GDGDB) [IDUA]
          • Sanfilippo syndrome A (GDGDB) [SGSH]
          • Sanfilippo syndrome B (GDGDB) [NAGLU]
          • Sanfilippo syndrome C (GDGDB) [HGSNAT]
          • Sanfilippo syndrome D (GDGDB) [GNS]
          • 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]