Phenotypes for disease #03801 (ICP3 (cholestasis, intrahepatic, of pregnancy, type 3 (ICP-3)), OMIM:614972)

4 entries on 1 page. Showing entries 1 - 4.
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AscendingPhenotype ID     

Phenotype details     

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Diagnosis/Definite     

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Age/Examination     

Age/Diagnosis     

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Individual ID     
0000041517 at least one typical episode of intrahepatic cholestasis of pregnancy (pruritus, abnormal serum liver tests with cholestatic pattern third trimester) resulting in fetal deaths in 3 women and spontaneous and progressive disappearance of cholestasis after delivery - - Familial, autosomal recessive - - - - - Johan den Dunnen 00054854
0000041518 2 live births, 2 lost pregnancies; pruritus started 15w, fetal distress (meconium staining amniotic fluid or fetal heart rate abnormality); delivery 35w6d; max. levels ALT 163 U/l (<28), yGT 50 (<30), U/l BA 237 mM (<6) - - Isolated (sporadic) - - - - - Johan den Dunnen 00054855
0000143334 ICP, endoscopic sphincterotomy, disturbance of liver function, intense pruritus, itching, ursodeoxycholic acid treatment Intrahepatic cholestasis of pregnancy Intrahepatic cholestasis of pregnancy Familial, autosomal dominant - - 34y - - Minh Tuan Huynh 00181082
0000143335 ICP of 24 weeks of gestation, intense pruritus at night (trunk and lower limbs), elevated AST, ALT), bile acids of 50µmol/L. Mother had history of intrahepatic cholestasis of pregnancy. Intrahepatic microlithiasis on imaging, ursodeoxycholic acid treatment Intrahepatic cholestasis of pregnancy Intrahepatic cholestasis of pregnancy Familial, autosomal dominant 21y 21y - - - Minh Tuan Huynh 00181083
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