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Ontology Browser

Term:
syndromic X-linked intellectual disability (DOID:0060309)
Annotations: Rat: (585) Mouse: (595) Human: (747) Chinchilla: (520) Bonobo: (611) Dog: (591) Squirrel: (544) Pig: (587)
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 +   
Lesch-Nyhan syndrome +   
Lujan Fryns Syndrome  
Menkes disease +   
Mental Retardation X-Linked, South African Type 
Mental Retardation, X-Linked 102  
Mental Retardation, X-Linked 95  
Mental Retardation, X-Linked, Syndromic, Zdhhc9-Related 
Mental Retardation, X-Linked, Syp-Related 
Mental Retardation, X-Linked, with Isolated Growth Hormone Deficiency  
methylmalonic acidemia and homocysteinemia cblX type  
mucopolysaccharidosis II  
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  
Stocco dos Santos Syndrome  
syndromic microphthalmia 1  
syndromic X-linked intellectual disability +   
A syndromic intellectual characterized by an X-linked inheritance pattern. (DO)
Tranebjaerg Svejgaard syndrome 
Wittwer Syndrome  
X-linked intellectual disability-psychosis-macroorchidism syndrome  
X-Linked Mental Retardation Gustavson Type 
X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance  
X-Linked Mental Retardation with Panhypopituitarism  

Synonyms
Exact Synonyms: syndromic X-linked mental retardation
Primary IDs: RDO:9004982
Xrefs: OMIM:PS309510
Definition Sources: http://en.wikipedia.org/wiki/X-linked_intellectual_disability "DO"

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.