Phenotypes for disease #05465 (del 22q11.2 (chromosome deletion syndrome 22q11.2, distal), OMIM:611867)

4 entries on 1 page. Showing entries 1 - 4.
Legend   How to query  

AscendingPhenotype ID     

Diagnosis/Initial     

Diagnosis/Definite     

Phenotype details     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000139188 - - Malignant rhabdoid tumor of the soft tissue (MRT) / at birth Familial - - - - - Julia Lopez 00174115
0000139189 - - RTK: kidney Familial - - 8m - - Julia Lopez 00174253
0000139208 - - - Familial - - - - - Julia Lopez 00173998
0000139209 - - - Familial - - - - - Julia Lopez 00173999
Legend   How to query  


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