Legend:

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

'Stomatognathic Diseases'  (Integration tree)

Pathogenesis

• Genetic disorders of glycan degradation

Disorders by systems

• Genetic disorders of glycan degradation (by systems, signs and symptoms)
  • Diseases
    • Stomatognathic Diseases
      • Mouth Diseases
        • Periodontal Diseases
          • Gingival Diseases
            • Gingival Overgrowth
              • Gingival Hyperplasia
                • Alpha-mannosidosis (GDGDB) [MAN2B1]
                • Sialidosis (GDGDB) [NEU1]
                • Mucolipidosis II (alpha/beta) (GDGDB) [GNPTAB]
                • GM1-gangliosidosis, type I (GDGDB) [GLB1]
                • GM1-gangliosidosis, type II (GDGDB) [GLB1]
                • GM1-gangliosidosis, type III (GDGDB) [GLB1]
        • Tongue Diseases
          • Macroglossia
            • Alpha-mannosidosis (GDGDB) [MAN2B1]
            • Hurler syndrome (GDGDB) [IDUA]
            • Hurler-Scheie syndrome (GDGDB) [IDUA]
            • Scheie syndrome (GDGDB) [IDUA]
            • Mucopolysaccharidosis II (GDGDB) [IDS]
            • Mucopolysaccharidosis VI (GDGDB) (GDGDB) [ARSB]
            • Mucopolysaccharidosis VII (GDGDB) [GUSB]
            • Pompe disease (GDGDB) [GAA]
              • Pompe disease, infantile-onset form [GAA]
      • Stomatognathic System Abnormalities
        • Maxillofacial Abnormalities
          • Aspartylglucosaminuria (GDGDB) [AGA]
          • Fucosidosis (GDGDB) [FUCA1]
          • Alpha-mannosidosis (GDGDB) [MAN2B1]
          • Beta-mannosidosis (GDGDB) [MANBA]
          • Sialidosis (GDGDB) [NEU1]
          • Galactosialidosis (GDGDB) [CTSA]
          • 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]
          • 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]
          • GM1-gangliosidosis, type I (GDGDB) [GLB1]
          • GM1-gangliosidosis, type II (GDGDB) [GLB1]
          • GM1-gangliosidosis, type III (GDGDB) [GLB1]
          • Gaucher disease, type II (GDGDB) [GBA]
            • Gaucher disease, type II, perinatal lethal form [GBA]
          • Multiple sulfatase deficiency (GDGDB) [SUMF1]