Phenotypes for disease #04039 (JBTS21 (Joubert syndrome, type 21 (JBTS-21)), OMIM:615636)

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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     
0000060430 Joubert syndrome 21 (OMIM:615636) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080861
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