Phenotypes for disease #02506 (NPHP3 (nephronophthisis, type 3 (NPHP-3)), OMIM:604387)

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     
0000129177 congenital hepatic fibrosis end stage renal disease - - Familial, autosomal recessive - - - - - John Sayer 00164068
0000129178 Severe chronic tubule-interstitial damage with atrophy of tubules, interstitial fibrosis and moderate interstitial inflammation Hypertension End stage renal disease 15 years - - Familial, autosomal recessive - - - - - John Sayer 00164069
0000129822 congenital hepatic fibrosis end stage renal disease Nephronophthisis Nephronophthisis Familial, autosomal recessive 20y - - 13y - John Sayer 00164805
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