Phenotypes for disease #04189 (NPHPRC (nephronophthisis-related ciliopathy (NPHP-RC)))

4 entries on 1 page. Showing entries 1 - 4.
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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     
0000025786 see paper; 11m-hepatic fibrosis; 14y-end-stage renal disease (ESRD) from NPHP; ... - - Isolated (sporadic) - - - - - Johan den Dunnen 00032320
0000025787 see paper; hepatic fibrosis; 2y-liver transplantation; no retinal degeneration, no cerebellar vermis hypoplasia, no hydrocephalus, no obesity, no bone disease - - Isolated (sporadic) - - - - - Johan den Dunnen 00032321
0000161683 increased echogenicity, medullary cysts, proteinuria, cortical deafness, atrial septal defect, growth retardation, short stature, coloboma, aplasia of vermis, corpus callosum hypoplasia; 5y-end-stage renal disease nephronophthisis - Familial, autosomal recessive - - - - - Johan den Dunnen 00213208
0000161684 NPHP, nonselective proteinuria, end-stage renal disease since infancy, sensorineural deafness, hepatosplenomegaly, short stature, anemia, thrombocytopenia, osteopenia, rickets; 2y-renal biopsy microcystic dilatation of tubules, immature glomeruli nephronophthisis - Familial, autosomal recessive - - - - - Johan den Dunnen 00213209
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