NIPTy MHLW-Designated Intractable Diseases Plan List

The NIPTy MHLW-Designated Intractable Diseases Plan is a practical and well-balanced option designed to efficiently screen for major chromosomal abnormalities that parents wish to confirm before birth. In addition to screening for Chromosomes 13, 18, and 21, fetal gender, and 23 types of microdeletion/duplication syndromes, we offer three plans tailored to your specific needs, which can also cover “All Chromosome Partial Deletion/Duplication Syndromes” and even “Aneuploidies of Chromosomes 1 to 22.” You can select the most appropriate test based on your budget and desired scope of information.

Screening Plan Comparison

Our NIPT Track Record Over 75,000 cases

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Our NIPT Track Record

68,000 cases

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Comprehensive Screening for Risks Across All Chromosomes

Aneuploidies of Chromosomes 1 to 22 Sex Chromosomes / Fetal Gender (Singletons) Presence/Absence of Y Chromosome (Twins) All Chromosome Partial Deletion / Duplication Syndromes 23 Types of Microdeletion / Duplication Syndromes

F23

270,000 JPY

297,000 JPY (incl. tax)

RecommendedThe Signature Choice Selected by Most Expectant Mothers

Aneuploidies of Chromosomes 13, 18, 21 Sex Chromosomes / Fetal Gender (Singletons) Presence/Absence of Y Chromosome (Twins) All Chromosome Partial Deletion / Duplication Syndromes 23 Types of Microdeletion / Duplication Syndromes

G23

240,000 JPY

264,000 JPY (incl. tax)

Thorough Coverage of 3 Core Conditions + 23 Microdeletions

Aneuploidies of Chromosomes 13, 18, 21 Sex Chromosomes / Fetal Gender (Singletons) Presence/Absence of Y Chromosome (Twins) 23 Types of Microdeletion / Duplication Syndromes

A23

180,000 JPY

198,000 JPY (incl. tax)

Comprehensive Screening for Risks Across All Chromosomes

F23

270,000 JPY

297,000 JPY (incl. tax)

RecommendedThe Signature Choice Selected by Most Expectant Mothers

G23

240,000 JPY

264,000 JPY (incl. tax)

Thorough Coverage of 3 Core Conditions + 23 Microdeletions

Aneuploidies of Chromosomes 13, 18, 21 Sex Chromosomes / Fetal Gender (Singletons) Presence/Absence of Y Chromosome (Twins) 23 Types of Microdeletion / Duplication Syndromes

A23

180,000 JPY

198,000 JPY (incl. tax)

Optional Services

Choosing to know earlier, without waiting for 10 weeks.

Early NIPT (Under 10 weeks of pregnancy)

11,000 JPY

(incl. tax)

Arrived samples are immediately allocated to the next testing slot.

Priority Delivery Service (Kakuyakubin)

44,000 JPY

(incl. tax)

July 2026, the next generation of screening begins.

NIPTy-MONO A screening test evaluating over 200 single-gene disorders. Scheduled for introduction from July 2026 onward.

330,000 JPY

(incl. tax)

Carrier Screening Test 231

Screening autosomal recessive genes for born children.

For Born Children Carrier Screening Test 231 We offer autosomal recessive gene testing at a special price for children born to mothers who underwent NIPT at Hiro Clinic.

*Generio Points issued during NIPT screening can also be utilized.
*The official start date will be announced as soon as it is finalized.

220,000 JPY

(incl. tax) Optional Price

Preparing for the future together as a couple.

For Parents Undergoing NIPT Carrier Screening Test 231 (Couple/Pair Test) We offer autosomal recessive gene screening as an option to accompany Hiro Clinic’s standard plans.

*Only matched carrier traits will be reported. The official start date will be announced as soon as it is finalized.

220,000 JPY

(incl. tax) Overseas Testing Optional Price

Ultrasound Examination

Omiya Station Clinic Osaka Station Clinic

Gynecology Only

11,000 JPY (incl. tax)

Amniocentesis Support (Sign-up available on the day of testing only)

Lite

Subsidizes testing costs up to 100,000 JPY

3,300 JPY (incl. tax)

Standard

Subsidizes testing costs up to 200,000 JPY

5,500 JPY (incl. tax)

Wide

Subsidizes testing costs up to 300,000 JPY

11,000 JPY (incl. tax)

Other Options

Consultations Outside Regular Hours In-person or remote (20 mins)

4,400 JPY (incl. tax)

Mailing of Test Results Delivery via simplified registered mail

3,300 JPY (incl. tax)

The F143 MONO Plan is our most comprehensive premium plan, covering everything from Chromosomes 1 to 22, intellectual disabilities, infertility factors, and miscarriage risks. Please note that “NIPTy-MONO,” which screens for over 200 single-gene disorders, is scheduled to be introduced from July 2026 onward.

The F143 Plan includes Chromosomes 1 to 22 + intellectual disabilities + infertility factors, making it a highly popular and well-balanced plan with broad coverage.

*NIPT screening is a voluntary, private clinical service. It is fully self-funded, and standard health insurance cannot be applied.

*Optional services cannot be purchased or used independently without a base screening plan.

Payment Information

We accept credit card payments only. Accepted cards: JCB, AMEX, Diners Club, UnionPay (银联), VISA, MasterCard, Discover

Our NIPT Track Record Over 75,000 cases

Check Availability & Book Now

Our NIPT Track Record

68,000 cases

Book an Appointment ▶︎▶︎▶︎