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Human Disease

mucopolysaccharidosis IV

Term ID
DOID:12804
Synonyms
  • chondroosteodystrophy
  • deficiency of chondroitinsulphatase
  • deficiency of N-acetylgalactosamine-6-sulphatase
  • galactosamine-6-sulfatase deficiency
  • Morquio A disease
  • Morquio syndrome A
  • Mucopolysaccharidosis, MPS-IV
  • Osteochondrodystrophy
Definition
A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzymes galactose 6-sulfate sulfatase (Type A) or beta-galactosidase (Type B) needed to break down the keratan sulfate sugar chain. http://en.wikipedia.org/wiki/Morquio_syndrome
References
  • ICD10CM:E76.219
  • MESH:D009085
  • NCI:C61263
  • SNOMEDCT_US_2023_03_01:378007
  • UMLS_CUI:C0026707
Ontology
Human Disease   ( DOID:12804 )
Relationships
is a type of
has subtype
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Genes Involved
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