Phenotypes for disease #03900 (CPPB2 (precocious puberty, central, type 2 (CPPB-2)), OMIM:615346)

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     
0000061014 - - - Familial, autosomal dominant - - - - - Johan den Dunnen 00038513
0000322862 Generalized non-motor (absence) seizure, Neurodevelopmental delay, Precocious puberty - - Unknown 10y - - - - Andreas Laner 00432294
Legend   How to query  


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