Phenotypes for disease #01257 (PAPRS (papillorenal syndrome (PAPRS)), OMIM:120330)

5 entries on 1 page. Showing entries 1 - 5.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Owner     

Individual ID     
0000273630 HP:0030515 HP:0000613 HP:0001123 HP:0000639 HP:0012795 syndrome, papillorenal (PAPRS) - Familial, autosomal dominant - - - - - Jinu Han 00379776
0000295603 microphthalmia, retinal detachment, optic nerve aplasia. OS: iris coloboma, cataract, optic nerve aplasia, Neurodevelopmental delay, hypotonia, abnormality of the pinna. microphthalmia, retinal detachment papillorenal syndrome Familial, autosomal dominant 00y04m - - microphthalmia (HP:0000568) - Miriam Erandi Reyna-Fabián 00402842
0000300859 bilateral vesicoureteral reflux, chronic renal failure, bilateral renal hypodysplasia, mild hypertrophy bladder neck; ocular and/or ear phenotype - - Isolated (sporadic) - - - - - Susanna Negrisolo 00408740
0000300860 renal cystic hypodysplasia, poor growth, developmental delay; one twin cataract, coloboma - - Isolated (sporadic) - - - - - Susanna Negrisolo 00408741
0000323089 bilateral renal hypodysplasia, vesicoureteral reflux, hearing loss papillorenal syndrome PAPRS Isolated (sporadic) - - - - - Susanna Negrisolo 00432527
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