Legend:

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

'Skin and Connective Tissue Diseases'  (Integration tree)

Pathogenesis

• Genetic disorders of glycan degradation

Disorders by systems

• Genetic disorders of glycan degradation (by systems, signs and symptoms)
  • Diseases
    • Skin and Connective Tissue Diseases
      • Connective Tissue Diseases
        • Cutis Laxa
          • Aspartylglucosaminuria (GDGDB) [AGA]
        • Mucinoses
          • Hurler syndrome (GDGDB) [IDUA]
          • Hurler-Scheie syndrome (GDGDB) [IDUA]
          • Scheie syndrome (GDGDB) [IDUA]
          • Mucopolysaccharidosis II (GDGDB) [IDS]
          • Mucopolysaccharidosis III
          • Mucopolysaccharidosis IV
          • Mucopolysaccharidosis VI (GDGDB) (GDGDB) [ARSB]
          • Mucopolysaccharidosis VII (GDGDB) [GUSB]
      • Skin Diseases
        • Skin Abnormalities
          • Ichthyosis
            • Gaucher disease, type II (GDGDB) [GBA]
              • Gaucher disease, type II, perinatal lethal form [GBA]
            • Multiple sulfatase deficiency (GDGDB) [SUMF1]
          • Gaucher disease, type II (GDGDB) [GBA]
            • Gaucher disease, type II, perinatal lethal form [GBA]
        • Sweat Gland Diseases
          • Hypohidrosis
            • Fabry disease (GDGDB) [GLA]
        • Fabry disease (GDGDB) [GLA]