DNAH9 Gene Primary ciliary dyskinesia, DNAH9 related NGS Genetic Test
Short Name: DNAH9 PCD NGS Test
DNAH9 Gene Primary ciliary dyskinesia, DNAH9 related NGS Genetic Test test available at DNA Labs India for ₹20,000. Uses Next-Generation Sequencing (NGS) on Blood or Extracted DNA or One drop Blood on FTA Card samples. Results in 3 to 4 Weeks. Free home collection in 300+ cities across India.
🩺 Medically Reviewed By
Dr SULOCHANA HEMCHANDRA HOLLA
Consultant Medical Geneticist · Reg: 8532
Last reviewed: September 7, 2026
Overview
The purpose of the DNAH9 Gene NGS Genetic Test is to detect mutations in the DNAH9 gene associated with Primary Ciliary Dyskinesia (PCD). This test helps in confirming a diagnosis of PCD, differentiating it from other respiratory conditions, guiding treatment decisions, and providing genetic counseling for affected families. It is recommended for individuals with symptoms of PCD or a family history of the disorder.
- Test Code
- 4789
- Price
- ₹20,000
- Sample Type
- Blood or Extracted DNA or One drop Blood on FTA Card
- Result Time
- 3 to 4 Weeks
- Fasting Required
- No
- Method
- Next-Generation Sequencing (NGS)
Sample Collection
No specific preparation required. Provide clinical history and genetic counseling if needed.
Method: Venipuncture
Laboratory Analysis
Blood sample collected via venipuncture or use of FTA card for one drop of blood.
Report Delivery
Apply pressure to the puncture site to prevent bleeding. Store sample as per instructions.
Timeline: 3 to 4 Weeks
Patient Instructions
About This Test
Who Should Get This Test
The purpose of the DNAH9 Gene NGS Genetic Test is to detect mutations in the DNAH9 gene associated with Primary Ciliary Dyskinesia (PCD). This test helps in confirming a diagnosis of PCD, differentiating it from other respiratory conditions, guiding treatment decisions, and providing genetic counseling for affected families. It is recommended for individuals with symptoms of PCD or a family history of the disorder.
How to Prepare
- Use sterile equipment for blood collection
- Label sample correctly with patient details
- Transport sample at ambient room temperature
Doctor's Notes
Reviewed by Dr SULOCHANA HEMCHANDRA HOLLA — MBBS, MD (Medical Genetics) · Reg. No. 8532
"Genetic testing for DNAH9 mutations is crucial for accurate diagnosis of Primary Ciliary Dyskinesia, enabling targeted treatment and management to improve patient outcomes."
Last medically reviewed: September 7, 2026
Test Parameters & Specifications
Sample Stability
- Hemolyzed or clotted samples
- Insufficient sample volume
- Incorrect labeling or documentation
Understanding Your Results
Pathogenic variant detected
Confirms diagnosis of DNAH9-related PCD. Genetic counseling and targeted management recommended.
No pathogenic variant detected
PCD due to DNAH9 mutations unlikely. Consider testing for other PCD-associated genes or clinical evaluation.
Consult a healthcare provider if you experience chronic respiratory symptoms, infertility, or have a family history of PCD. After receiving test results, discuss them with a genetic specialist or ENT doctor for appropriate management.
Limitations
- ⚠May not detect all types of mutations in the DNAH9 gene
- ⚠Results require interpretation by a genetic specialist
- ⚠Does not rule out other genetic causes of PCD
Risks & Considerations
- ●Minimal risks from blood draw, such as bruising or infection
- ●Psychological impact of genetic results
Interfering Factors
- ●Sample contamination
- ●Degraded DNA
- ●Incorrect sample collection or handling
Compare With Similar Tests
| Test | DNAH9 Gene Primary ciliary dyskinesia, DNAH9 related NGS Genetic Test | DNAI1 Gene PCD NGS Test | DNAH5 Gene PCD NGS Test | CCDC39 Gene PCD NGS Test | PCD Panel NGS Test |
|---|---|---|---|---|---|
| Comparison | DNAH9 Gene Primary ciliary dyskinesia, DNAH9 related NGS Genetic Test | Tests for mutations in DNAI1 gene, another common cause of PCD. | Targets DNAH5 gene mutations associated with PCD. | Detects mutations in CCDC39 gene linked to PCD. | Comprehensive panel testing multiple genes for PCD diagnosis. |
Frequently Asked Questions
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₹20,000Reference Laboratory Services
We serve as a reference laboratory for hospitals and clinics across India. Send samples from your facility with same-day pickup, priority processing, and results delivered through our online portal. Competitive institutional pricing available.
Your Data Privacy
Your medical data is protected under Indian law.
✓ Stored in India: All patient records are stored on servers located in India. No data is transferred outside the country.
✓ DPDP Act Compliant: Under the Digital Personal Data Protection Act 2023, you can request deletion of your records at any time by contacting support.
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