Disease #05159 (MRXS34 (mental retardation, X-linked, syndromic, type 34), OMIM:300967)

Official abbreviation MRXS34
Name mental retardation, X-linked, syndromic, type 34
OMIM ID 300967
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene NONO
Associated tissues -
Disease features -
Remarks -
Date created 2016-04-28 17:27:30 +02:00 (CEST)
Date last edited 2022-09-28 08:54:55 +02:00 (CEST)


Individuals

1 entry on 1 page. Showing entry 1.
Legend   How to query  

AscendingIndividual ID     
ID_report     
Reference     
Remarks     
Gender     
Consanguinity     
Country     
Population     
Age at death     
VIP     
Data_av     
Treatment     
Disease     
Phenotype details     
Genes screened
Variants in genes
Variants     
Panel size     
Owner     
00417862 - - - M - China - - - - - MRXS34 tricuspid regurgitation; abnormal myocardium morphology; ventricular septal defect; anemia; hepatic hemangioma; postnatal growth retardation; noncompaction cardiomyopathy, atrial septal defect NONO NONO 1 1 Xiaoyan Peng
Legend   How to query  

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
  Powered by LOVD v.3.0 Build 30b
LOVD software ©2004-2024 Leiden University Medical Center
Database contents © by their respective submitters and curators
 There are currently no updates.