2026 ICD-10-CM Diagnosis Code Q69Polydactyly
Q69 is a non-billable ICD-10-CM category code for polydactyly, so it cannot be submitted on claims. Use a more specific code from this category instead, such as Q69.0, Q69.1, Q69.2, and Q69.9.
Code Identity
Code Classification
Specific Coding for PolydactylyOverview
Clinical InformationClinical
Polydactyly
a congenital anomaly of the hand or foot, marked by the presence of supernumerary digits.Short Rib-Polydactyly Syndrome
a syndrome inherited as an autosomal recessive trait and incompatible with life. the main features are narrow thorax, short ribs, scapular and pelvic dysplasia, and polydactyly.Smith-Lemli-Opitz Syndrome
an autosomal recessive disorder of cholesterol metabolism. it is caused by a deficiency of 7-dehydrocholesterol reductase, the enzyme that converts 7-dehydrocholesterol to cholesterol, leading to an abnormally low plasma cholesterol. this syndrome is characterized by multiple congenital abnormalities, growth deficiency, and intellectual disability.
Patient EducationClinical
Birth Defects
A birth defect is a problem that happens while a baby is developing in the mother's body. Most birth defects happen during the first 3 months of pregnancy. One out of every 33 babies in the United States is born with a birth defect.
The full article covers:
- What are birth defects?
- What causes birth defects?
- Who is at risk of having a baby with birth defects?
- How are birth defects diagnosed?
- What are the treatments for birth defects?
- Can birth defects be prevented?
Read the full article at MedlinePlus
Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.
