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Ontology Browser

Term:
mucopolysaccharidosis II (DOID:12799)
Annotations: Rat: (1) Mouse: (1) Human: (2) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
adrenoleukodystrophy +   
Aldred Syndrome 
Allan-Herndon-Dudley syndrome  
alpha thalassemia-X-linked intellectual disability syndrome  
Arena Syndrome 
Atkin Syndrome  
Charcot-Marie-Tooth disease X-linked recessive 4  
Chromosome Xp11.3 Deletion Syndrome  
CK syndrome  
Classical Lissencephalies and Subcortical Band Heterotopias +   
Coffin-Lowry syndrome  
creatine transporter deficiency  
Danon disease  
Faciogenital Dysplasia with Attention Deficit-Hyperactivity Disorder 
FG syndrome +   
fragile X syndrome +   
INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, WITH PANHYPOPITUITARISM  
Lesch-Nyhan syndrome +   
Menkes disease +   
Mental Retardation X-Linked, South African Type 
Mental Retardation, X-Linked 102  
Mental Retardation, X-Linked, Syp-Related 
methylmalonic acidemia and homocysteinemia cblX type  
Mucopolysaccharidoses, Unclassified Types 
mucopolysaccharidosis I +   
mucopolysaccharidosis II  
A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme iduronate sulfatase. (DO)
mucopolysaccharidosis III +   
mucopolysaccharidosis IV +   
mucopolysaccharidosis IX  
mucopolysaccharidosis VI  
Mucopolysaccharidosis VIII 
Mucopolysaccharidosis X  
Mucopolysaccharidosis-Plus Syndrome  
non-syndromic X-linked intellectual disability +   
Plagiocephaly and X-Linked Mental Retardation 
Ppm-X Syndrome 
pyruvate decarboxylase deficiency +   
Rett syndrome +   
Roifman Syndrome  
severe congenital encephalopathy due to MECP2 mutation  
Sly syndrome  
syndromic microphthalmia 1  
syndromic X-linked intellectual disability +   
Tranebjaerg Svejgaard syndrome 
Wittwer Syndrome  
X-Linked Intellectual Developmental Disorder 95  
X-Linked Mental Retardation with Isolated Growth Hormone Deficiency  

Synonyms
Exact Synonyms: Hunter Syndrome ;   Hunter Syndrome Gargoylism ;   Hunter's syndrome ;   Hunters syndrome ;   I2S Deficiency ;   IDS DEFICIENCY ;   Iduronate 2 Sulfatase Deficiency ;   Iduronate Sulfatase Deficiency ;   MPS II ;   MPS II - Hunter syndrome ;   MPS2 ;   MUCOPOLYSACCHARIDOSIS, MPS-II ;   Mucopolysaccharidosis 2 ;   Mucopolysaccharidosis Type 2 ;   Mucopolysaccharidosis Type II ;   SIDS deficiency ;   deficiency of iduronate-2-sulphatase ;   sulfoiduronate sulfatase deficiency
Narrow Synonyms: mucopolysaccharidosis type II, mild form ;   mucopolysaccharidosis type II, severe form
Primary IDs: MESH:D016532
Alternate IDs: OMIM:309900
Xrefs: GARD:6675 ;   ICD10CM:E76.1 ;   NCI:C61260 ;   ORDO:580
Definition Sources: http://en.wikipedia.org/wiki/Hunter_syndrome "DO" "DO"

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