Bifid uvula is a fissure type embryopathy affecting the uvula at the back of the soft palate.
Comprehensive, easy-to-understand information about this condition
How we create this content →Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 7, 2026
Research studies investigating treatments and therapies for this condition.
Active Trials
Total Trials
Data from ClinicalTrials.gov Jan 7, 2026
The limited documentation surrounding bifid uvula is largely due to its rarity and the lack of systematic clinical studies. Conditions like bifid uvula, which affect a small number of individuals, often do not attract extensive research funding or focus, resulting in gaps in clinical characterization and understanding.
To better understand and manage bifid uvula, consider consulting with a specialist in genetics or a craniofacial surgeon who has experience in congenital conditions. While there are currently no specific patient organizations for bifid uvula, resources such as the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can provide valuable information and support. Additionally, genetic counseling may be beneficial for family planning and understanding inheritance patterns.
Actionable guidance for navigating care for bifid uvula
To better understand and manage bifid uvula, consider consulting with a specialist in genetics or a craniofacial surgeon who has experience in congenital conditions. While there are currently no specific patient organizations for bifid uvula, resources such as the Genetic and Rare Diseases Information Center (GARD) at rarediseases.info.nih.gov can provide valuable information and support. Additionally, genetic counseling may be beneficial for family planning and understanding inheritance patterns.
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 7, 2026
Consider asking your healthcare providers these condition-specific questions
Online Mendelian Inheritance in Man
European rare disease database
Genetic and Rare Diseases Info Center
AI-Generated Content: This summary was generated using AI. 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.