Morquio syndrome
Osteochondrodysplasia
Atypical chondrodystrophy
Brailsford-Morquio syndrome
Chondro-osteodystrophy
Chondrodystrophia tarda
Familial osseous dystrophy
Familial osteochondrodystrophy
Hereditary enchondral dysostosis
Keratan sulfaturia
Morquio-Suarez syndrome
Morquio-Ullrich disease
Osteochondrodystrophia deformans
Morquio disease
Mucopolysaccharidosis type IV
Osteochondrodystrophy
Morquio-Brailsford disease
Keratan sulphaturia
Morquio syndrome (disorder)
Mucopolysaccharidosis, MPS-IV
Morquio disease, NOS
Morquio syndrome, NOS
Osteochondrodysplasia, NOS
378007
http://purl.bioontology.org/ontology/SNOMEDCT/378007
0
C3754
Dystrophy
Courses
Bone structure
Severities
(Mucopolysaccharidosis: (& [gargoylism]/[Hunter][Hurler]/[lipochondrodyst]/[Maroteaux-Lamy]/[Morquio-Brailsford]/[osteochondrodystrophy]/[Sanfilippo]/[Scheie]) or (dysostos multi)
Mucopolysaccharidosis
Connective tissue hereditary disorder
Congenital connective tissue disorder
Autosomal recessive hereditary disorder
Hereditary disorder of musculoskeletal system
Osteodystrophy
Metabolic bone disease
Degenerative disorder
1
Congenital
Congenital Abnormality
Disease or Syndrome
D6-70240
T019
T047
C0029422
C0026707