Phenotypes for disease #00700 (JBTS5 (Joubert syndrome, type 5 (JBTS-5)), OMIM:610188)

3 entries on 1 page. Showing entries 1 - 3.
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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     
0000060447 Joubert syndrome 5 (OMIM:610188) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080878
0000239234 prenatal ultrasoud: Dandy-Walker malformation, hyperechogenic kidney, Molar tooth sign, heart abnormalities prenatal - Unknown - - - - - Andreas Laner 00315483
0000294775 Chronic kidney disease (HPO 0012622) horizontal gaze palsy (HPO 0000666) ptosis right eye (HPO 0007687) Molar tooth sign (HPO 0002419) Dandy Walker anomaly (HPO 0001305) Hyperechoic kidneys with loss of corticomedullary differentiation (HPO 0005565) Joubert syndrome Joubert syndrome type 5 Familial, autosomal recessive 02y 02y 00y00m01d - - John Sayer 00402012
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