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Ontology Browser

Term:
syndromic X-linked intellectual disability Shashi type (DOID:0060826)
Annotations: Rat: (1) Mouse: (1) Human: (2) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1) Naked Mole-rat: (1) Green Monkey: (1)
Parent Terms Term With Siblings Child Terms
Armfield syndrome  
Arts syndrome  
Basilicata-Akhtar syndrome  
Borjeson-Forssman-Lehmann syndrome  
Christianson syndrome  
corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome  
deafness-intellectual disability, Martin-Probst type syndrome  
female-restricted syndromic X-linked intellectual disability 99  
INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, HACKMANN-DI DONATO TYPE  
MEHMO syndrome  
Mental Retardation, X-Linked, Syndromic, Ube2a-Related 
Miles-Carpenter syndrome +   
Mullegama-Klein-Martinez syndrome  
Paganini-Miozzo syndrome  
Partington syndrome  
Prieto syndrome  
Raynaud-Claes syndrome  
Renpenning syndrome  
Schimke X-Linked Mental Retardation Syndrome 
Stocco Dos Santos type X-linked intellectual disability  
syndromic X-linked intellectual developmental disorder 37  
syndromic X-linked intellectual developmental disorder Bain type  
syndromic X-linked intellectual disability 12 
syndromic X-linked intellectual disability 14  
syndromic X-linked intellectual disability 17 
syndromic X-linked intellectual disability 34  
syndromic X-linked intellectual disability 5  
syndromic X-linked intellectual disability 7 
syndromic X-linked intellectual disability 94  
syndromic X-linked intellectual disability Abidi type 
syndromic X-linked intellectual disability Cabezas type  
syndromic X-linked intellectual disability Chudley-Schwartz type 
syndromic X-linked intellectual disability Claes-Jensen type  
syndromic X-linked intellectual disability Hedera type  
syndromic X-linked intellectual disability Lubs type  
syndromic X-linked intellectual disability Najm type  
syndromic X-linked intellectual disability Nascimento type  
syndromic X-linked intellectual disability Pilorge type  
syndromic X-linked intellectual disability Raymond type  
syndromic X-linked intellectual disability Shashi type  
A syndromic X-linked intellectual disability characterized by moderate intellectual deficit, obesity, macroorchidism and a characteristic facies that has_material_basis_in mutation in the RBMX gene on chromosome Xq26. (DO)
syndromic X-linked intellectual disability Shrimpton type 
syndromic X-linked intellectual disability Siderius type  
syndromic X-linked intellectual disability Snyder type  
syndromic X-linked intellectual disability Turner type  
syndromic X-linked intellectual disability type 10  
syndromic X-linked intellectual disorder Lujan-Fryns-type  
Syndromic X-Linked Mental Retardation 33  
syndromic X-linked mental retardation 35  
syndromic X-linked mental retardation Hough type  
Tonne-Kalscheuer syndrome  
Van Esch-O'Driscoll syndrome  
Wilson-Turner syndrome  
X-linked Aarskog syndrome  
X-linked intellectual developmental disorder 108  
X-linked intellectual developmental disorder 109  
X-Linked Intellectual Developmental Disorder 110  
X-Linked Intellectual Developmental Disorder 112  
X-Linked Intellectual Developmental Disorder 113  
X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome  
X-linked intellectual disability-psychosis-macroorchidism syndrome  
X-linked intellectual disability-short stature-overweight syndrome  
X-linked mental retardation Gustavson type  
X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance  
X-linked mental retardation-hypotonic facies syndrome-1  

Synonyms
Exact Synonyms: MRXS11 ;   MRXSSH ;   SMRXS ;   Shashi X-linked mental retardation syndrome ;   X-linked mental retardation, Shashi type ;   orofaciodigital syndrome, Shashi type ;   syndromic X-linked intellectual disability type 11 ;   syndromic X-linked mental retardation 11 ;   syndromic X-linked mental retardation 11, Shashi type ;   syndromic intellectual developmental disorder 11, Shashi type
Primary IDs: MESH:C537135
Alternate IDs: OMIM:300238
Xrefs: ORDO:85286
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/10677307 "DO" "DO", https://www.ncbi.nlm.nih.gov/pubmed/25256757 "DO" "DO"

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