Disease #00771 (WTS (Wilson-Turner syndrome), OMIM:309585)

Official abbreviation WTS
Name Wilson-Turner syndrome
OMIM ID 309585
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene LAS1L
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2024-05-12 18:23:41 +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     
00435162 259413 - - M no Germany - - - - - WTS Intellectual disability, mild, Obesity, Tall stature, Depression, Autistic behavior, Motor delay, Short attention span LAS1L LAS1L 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.