Disease #00229 (PWS (Prader-Willi syndrome (PWS)), OMIM:176270)

Official abbreviation PWS
Name Prader-Willi syndrome (PWS)
OMIM ID 176270
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 2
Associated with 2 genes NDN, SNRPN
Associated tissues -
Disease features -
Remarks -
Date created 2013-10-09 19:21:42 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


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     
00305399 130504 - - M ? Germany - - - - - PWS Makrosomie, Adipositas TMEM43 TMEM43 1 1 Andreas Laner
Legend   How to query  


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