Phenotypes for disease #00920 (JBTS3 (Joubert syndrome, type 3 (JBTS-3)), OMIM:608629)

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     
0000207255 - - 2017-11-17 Familial, autosomal recessive - 24y - - - Jinu Han 00269432
0000319165 Global developmental delay, Intellectual disability, Cerebellar vermis hypoplasia, Molar tooth sign on MRI, Protruding tongue, Neoplasm of the skin, Hypotonia, Strabismus, Absent speech - - Familial, autosomal recessive 06y - - - - Andreas Laner 00428260
Legend   How to query  


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