Short answer · Medically reviewed summary · Last updated: 2026-05-08
Asherman’s Syndrome is clinically classified under ICD-10 code N85.6, which specifically denotes intrauterine synechiae. In the older ICD-9 classification system, this condition was coded as 621.5. What is the clinical definition of Asherman’s Syndrome? Asherman’s Syndrome is an acquired uterine condition characterized by the formation of intrauterine adhesions (scar tissue) or synechiae within the uterine cavity.
ICD10 code of Asherman's Syndrome and ICD9 code
ICD-10 and ICD-9 codes for Asherman's Syndrome, with classification details for clinicians, coders and patients.
Asherman’s Syndrome is clinically classified under ICD-10 code N85.6, which specifically denotes intrauterine synechiae. In the older ICD-9 classification system, this condition was coded as 621.5.
What is the clinical definition of Asherman’s Syndrome?
Asherman’s Syndrome is an acquired uterine condition characterized by the formation of intrauterine adhesions (scar tissue) or synechiae within the uterine cavity. These bands of scar tissue can cause the walls of the uterus to stick together, potentially leading to menstrual irregularities, such as amenorrhea or hypomenorrhea, as well as recurrent pregnancy loss or secondary infertility. Asherman’s Syndrome is most commonly a complication following invasive uterine procedures.
How is Asherman’s Syndrome typically caused?
The development of Asherman’s Syndrome is almost exclusively associated with trauma to the basal layer of the endometrium. The most frequent triggers include:
- Dilatation and curettage (D&C) procedures, particularly those performed shortly after pregnancy.
- Cesarean sections or other uterine surgeries (myomectomy).
- Infection of the endometrium (endometritis).
- Manual removal of the placenta.
How is Asherman’s Syndrome diagnosed?
Diagnosing Asherman’s Syndrome requires visualization of the uterine cavity. The gold standard for diagnosis is hysteroscopy, which allows a physician to directly view the synechiae. Other diagnostic methods include a hysterosalpingogram (HSG), which uses contrast dye to outline the uterine cavity, or a saline infusion sonohysterogram, which can identify structural irregularities associated with Asherman’s Syndrome.
What is the emotional impact of Asherman’s Syndrome?
Living with Asherman’s Syndrome can be deeply distressing, especially for those hoping to conceive. At DiseaseMaps.org, 39 community members have shared their experiences with Asherman’s Syndrome, highlighting the importance of finding support from others who understand the unique reproductive challenges associated with this diagnosis.
Next steps
- Consult a reproductive endocrinologist or a gynecologic surgeon specializing in hysteroscopic adhesiolysis.
- Request a referral for a hysteroscopy if you have symptoms of Asherman’s Syndrome following uterine surgery.
- Connect with the community of 39 members on DiseaseMaps.org to share experiences and coping strategies.
Medical disclaimer: This content is for informational purposes only and does not constitute professional medical advice, diagnosis, or treatment; always seek the guidance of your physician regarding any medical condition.
References
- NIH Genetic and Rare Diseases Information Center (GARD) - Asherman Syndrome.
- Orphanet: Portal for rare diseases and orphan drugs (ORPHA:99926).
- World Health Organization (WHO) International Classification of Diseases (ICD-10/ICD-11).
- The American College of Obstetricians and Gynecologists (ACOG) clinical guidance on intrauterine adhesions.
