Legend:

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

'Respiratory Tract Infections'  (Integration tree)

Pathogenesis

• Genetic disorders of glycan degradation

Disorders by systems

• Genetic disorders of glycan degradation (by systems, signs and symptoms)
  • Diseases
    • Respiratory Tract Diseases
      • Respiratory Tract Infections
        • Aspartylglucosaminuria (GDGDB) [AGA]
        • Fucosidosis (GDGDB) [FUCA1]
        • Alpha-mannosidosis (GDGDB) [MAN2B1]
        • Beta-mannosidosis (GDGDB) [MANBA]
        • Mucolipidosis II (alpha/beta) (GDGDB) [GNPTAB]
        • Mucolipidosis III (alpha/beta) (GDGDB) [GNPTAB]
        • Hurler syndrome (GDGDB) [IDUA]
        • Hurler-Scheie syndrome (GDGDB) [IDUA]
        • 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]
        • Morquio syndrome A (GDGDB) [GALNS]
        • Morquio syndrome B (GDGDB) [GLB1]
        • Mucopolysaccharidosis VI (GDGDB) (GDGDB) [ARSB]
        • Mucopolysaccharidosis VII (GDGDB) [GUSB]
        • Niemann-Pick disease, type A (GDGDB) [SMPD1]
        • Niemann-Pick disease, type B (GDGDB) [SMPD1]
        • Niemann-Pick disease, type C1 (GDGDB) [NPC1]
        • Niemann-Pick disease, type C2 (GDGDB) [NPC2]
        • Combined saposin deficiency (GDGDB) [PSAP]
        • Pompe disease (GDGDB) [GAA]