Phenotypes for disease #05061 (WAS (Wiskott-Aldrich syndrome (WAS)), OMIM:301000)

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000303338 Thrombocytopenia (HP:0001873), Intracranial hemorrhage (HP:0002170) Thrombocytopenia Wiskott-Aldrich Syndrome Familial, X-linked recessive 00y01m 00y02m - - - Aysel Tekmenuray-Unal 00411262
0000350524 HP:0001873, HP:0001419, HP:0002721 WAS WAS Familial, X-linked recessive - - - - - Marketa Wayhelova 00464524
Legend   How to query  


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