Phenotypes for disease #00609 (JBTS17 (Joubert syndrome, type 17 (JBTS-17)), OMIM:614615)

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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000257289 Developmental delay,molar tooth sign and cerebellar vermis agenesis on MRI brain - - Familial, autosomal recessive - - - - - Anju Shukla 00361895
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