Phenotypes for disease #02022 (PKD4 (kidney, polycystic, disease, type 4, with/without hepatic disease (PKD4)), OMIM:263200)

7 entries on 1 page. Showing entries 1 - 7.
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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     
0000060403 Polycystic kidney and hepatic disease (OMIM:263200) - - Familial, autosomal recessive - - - - - Daniel Trujillano 00080834
0000210146 Hypertension CKD Congenital hepatic fibrosis - - Familial, autosomal recessive 04y - - - - John Sayer 00275525
0000210147 Hypertension CKD Congestive heart failure - - Familial, autosomal recessive 00y01m - - prenatal - John Sayer 00275526
0000210148 Hypertension Congenital hepatic fibrosis - - Familial, autosomal recessive 00y01m - - - - John Sayer 00275527
0000238693 oligohydramnios (HP:0001562), abnormality intrahepatic bile duct (HP:0011040), enlarged kidney (HP:0000105), polycystic kidney dysplasia (HP:0000113), congenital hepatic fibrosis (HP:0002612) - - Familial, autosomal recessive - - - - - Zhao SZ 00314937
0000238716 oligohydramnios (HP:0001562),enlarged kidney (HP:0000105) - PKD4 Familial, autosomal recessive - - - - - Zhao SZ 00314957
0000352022 Multiple congenital anomalies, bilateral palpable kidney masses, dysmorphic features. ARPKD ARPKD Familial, autosomal recessive 00y00m 00y00m 00y00m - - John Sayer 00466658
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