Phenotypes for disease #00838 (MRXSR (mental retardation, X-linked syndromic, Raymond type (MRXSR)), OMIM:300799)

3 entries on 1 page. Showing entries 1 - 3.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Birth_Details     

Protein     

Owner     

Individual ID     
0000120984 developmental delay, no epilepsy, hypotonia developmental delay MRXSR Isolated (sporadic) - - - - - - Joonhong Park 00147122
0000288015 see paper; ..., intellectual disability; early childhood severe growth failure, severe hypotonia, developmental delay; verbally aggressive, antisocial behavior intellectual disability MRXSR Unknown 13y - - - - - Juliana Mazzeu 00394439
0000312085 Obesity, Macrocephaly, Delayed speech and language development, Intellectual disability, Macrotia, Dysarthria, Incisor macrodontia - - Isolated (sporadic) 06y - - - - - Andreas Laner 00420838
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.