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Ontology Browser

Parent Terms Term With Siblings Child Terms
Mucopolysaccharidoses, Unclassified Types 
mucopolysaccharidosis I +   
mucopolysaccharidosis II  
mucopolysaccharidosis III +   
mucopolysaccharidosis IV +   
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. (DO)
mucopolysaccharidosis IX  
mucopolysaccharidosis VI  
Mucopolysaccharidosis VIII 
Mucopolysaccharidosis X  
Mucopolysaccharidosis-Plus Syndrome  
Sly syndrome  

Exact Synonyms: Eccentroosteochondrodysplasia ;   Eccentroosteochondrodysplasias ;   Galactosamine 6 Sulfatase Deficiency ;   Galactosamine-6-Sulfatase Deficiencies ;   Morquio Disease ;   Morquio Syndrome ;   Morquio Syndromes ;   Morquio's Disease ;   Morquio's Syndrome ;   Morquios Disease ;   Morquios Syndrome ;   Mucopolysaccharidosis 4 ;   deficiency of N-acetylgalactosamine-6-sulphatase ;   deficiency of chondroitinsulphatase ;   eccentro osteochondrodysplasia ;   eccentro-osteochondrodysplasias ;   mucopolysaccharidosis type IV ;   mucopolysaccharidosis, MPS-IV
Narrow Synonyms: chondroosteodystrophy ;   osteochondrodystrophy
Primary IDs: MESH:D009085
Xrefs: ICD10CM:E76.219 ;   NCI:C61263
Definition Sources: "DO" "DO"

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