Phenotypes for disease #00082 (JBTS9 (Joubert syndrome, type 9 (JBTS-9)), OMIM:612285)

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AscendingPhenotype ID     

Diagnosis/Initial     

Inheritance     

Age/Examination     

Diagnosis/Definite     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Phenotype details     

Protein     

Owner     

Individual ID     
0000321771 - Isolated (sporadic) - - - - neonatal - C2D2A Domenico Coviello 00431162
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