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Ontology Browser

Term:
non-syndromic X-linked intellectual disability (DOID:0050776)
Annotations: Rat: (36) Mouse: (38) Human: (43) Chinchilla: (38) Bonobo: (40) Dog: (40) Squirrel: (40) Pig: (40)
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  
autosomal dominant non-syndromic intellectual disability +   
autosomal recessive non-syndromic intellectual disability +   
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 +   
Menkes disease +   
Mental Retardation X-Linked, South African Type 
Mental Retardation, X-Linked 102  
Mental Retardation, X-Linked 95  
Mental Retardation, X-Linked, Syp-Related 
methylmalonic acidemia and homocysteinemia cblX type  
mucopolysaccharidosis II  
non-syndromic X-linked intellectual disability +   
A non-syndromic intellectual disability characterized by a X-linked inheritance pattern. (DO)
Plagiocephaly and X-Linked Mental Retardation 
Ppm-X Syndrome 
pyruvate decarboxylase deficiency +   
Rett syndrome +   
Roifman Syndrome  
severe congenital encephalopathy due to MECP2 mutation  
syndromic microphthalmia 1  
syndromic X-linked intellectual disability +   
Tranebjaerg Svejgaard syndrome 
Wittwer Syndrome  
X-Linked Mental Retardation Gustavson Type 
X-Linked Mental Retardation with Isolated Growth Hormone Deficiency  
X-Linked Mental Retardation with Panhypopituitarism  

Synonyms
Exact Synonyms: X-linked non-specific mental retardation
Primary IDs: MESH:C564490
Xrefs: OMIM:PS309530 ;   ORDO:777
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/7011032 "DO" "DO"

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