Billable / Specific Code
ICD-10-CM E20.810 is the diagnosis code for Autosomal dominant hypocalcemia. This code falls under the section "Disorders of other endocrine glands" within Chapter 4 — Endocrine, nutritional and metabolic diseases (E00-E89). It is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. Medical coders and healthcare providers use this code to document and classify diagnoses in electronic health records, insurance claims, and clinical databases.
Understanding where E20.810 sits in the ICD-10-CM classification helps ensure proper coding:
Yes, E20.810 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
E20.810 is the ICD-10-CM diagnosis code for "Autosomal dominant hypocalcemia". It is used by healthcare providers to classify and document this condition in medical records and insurance claims.
The parent code of E20.810 is E20.81 ("Hypoparathyroidism due to impaired parathyroid hormone secretion"). E20.810 provides a more specific classification within this category.
E20.810 is located in Section E20-E35 — "Disorders of other endocrine glands" within Chapter 4 of the ICD-10-CM Tabular List.
Use E20.810 when the patients documented diagnosis matches "Autosomal dominant hypocalcemia" and the clinical documentation supports this level of specificity. Always verify with the latest ICD-10-CM guidelines and payer requirements.
The ICD-10-CM code for Autosomal dominant hypocalcemia is E20.810.
Yes, E20.810 can be used as a primary diagnosis code since it is billable and specific.
E20.810 is in Chapter 4 of the ICD-10-CM Tabular List.
Yes, E20.810 is a valid ICD-10-CM code for the 2026 fiscal year, subject to official CMS updates.