Bardet Biedl Syndrome 6 10 Digenic C4017660
A rare genetic disorder affecting multiple body systems. It typically causes vision problems, obesity, extra fingers or toes, kidney issues, and learning difficulties. Management involves specialists to address each symptom.
Key facts at a glance
- ICD-10
- Q89.9
- ICD-11
- LA00.0
- Body system
- congenital
- Severity
- moderate
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Cone-rod dystrophy
(congenital)Generalized symptoms
(congenital)Noticeable symptoms that may vary in intensity over time.
Frequency: Common at all stages
Polydactyly
(congenital)Renal abnormality
(genitourinary)Primary hypogonadism
(endocrine)Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
Standard diagnostic workup
Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]
Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]
Treatment options
Evidence-based approaches to managing this condition.
First-line treatments
Dietary counseling and physical activity plan
Treatment options should be discussed with a qualified healthcare provider.
Multisystem surveillance program
Coordinated monitoring across specialties including ophthalmology, nephrology, and endocrinology to detect digenic inheritance complications early.
Corrective hand-foot surgery
Combined surgical approach to address polydactyly with careful pre-surgical planning due to potential variability in digenic presentation.
Additional treatment options
Low-vision adaptation strategies
Training in use of assistive devices, environmental modifications, and adaptive techniques to maintain independence with progressive vision loss.
lifestyleDevelopmental motor therapy
Therapeutic exercises and activities to improve balance, coordination, and fine motor control affected by syndromic features.
physical_therapyFamily support and education program
Comprehensive education about BBS variability in digenic inheritance and connection to support networks for psychosocial well-being.
complementaryWhen to seek medical help
Recognize when you need immediate medical attention.
Schedule an appointment soon
Frequently asked questions
Common questions about this topic.
What is Bardet Biedl Syndrome 6 10 Digenic C4017660?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy