Comprehensive, easy-to-understand information about this condition
How we create this content →Inheritance patterns describe how genetic conditions are passed from parents to children.
Inheritance patterns describe how genetic conditions are passed from parents to children.
The documentation for cholestasis, intrahepatic, of pregnancy, 1 is limited primarily due to its rarity and the recent identification of its genetic basis. As this condition affects a relatively small number of individuals, systematic clinical studies have been scarce, making it challenging to gather comprehensive data on its clinical features and management.
To navigate cholestasis, intrahepatic, of pregnancy, 1, consider consulting a maternal-fetal medicine specialist with experience in liver conditions during pregnancy. Genetic counseling is also recommended to discuss the implications of ATP8B1 variants for you and your family. While there are currently no patient organizations specifically for this condition, resources like the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov may provide valuable information and support. Engaging in clinical trials could also be an option to explore.
Currently, there is one active clinical trial related to cholestasis, intrahepatic, of pregnancy, 1. The details of this trial can be explored further at ClinicalTrials.gov. Unfortunately, there are no orphan drug designations for this condition at this time, indicating a lack of specifically approved treatments. However, participation in clinical trials may provide access to new therapies and contribute to the understanding of this condition.
Actionable guidance for navigating care for cholestasis, intrahepatic, of pregnancy, 1
To navigate cholestasis, intrahepatic, of pregnancy, 1, consider consulting a maternal-fetal medicine specialist with experience in liver conditions during pregnancy. Genetic counseling is also recommended to discuss the implications of ATP8B1 variants for you and your family. While there are currently no patient organizations specifically for this condition, resources like the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov may provide valuable information and support. Engaging in clinical trials could also be an option to explore.
Consider asking your healthcare providers these condition-specific questions
Helpful links for rare disease information and support
Inheritance patterns describe how genetic conditions are passed from parents to children.
Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 8, 2026
Consider asking your healthcare providers these condition-specific questions
Online Mendelian Inheritance in Man
Genetic and Rare Diseases Info Center
AI-Generated Content: This summary was generated using AI. Content has been fact-checked. Always consult with qualified healthcare providers for medical guidance.
Kisho delivers this disease record via API, including phenotypes (HPO), genes, orphan drug designations, screening status, and PAG mapping, with version history and governance.