Autosomal dominant hypocalcemia
Billable / specific
E20.810 is a billable, specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes in FY2027.
Inclusion terms
Applicable to
- Autosomal dominant hypocalcemia type 1 (ADH1)
- Autosomal dominant hypocalcemia type 2 (ADH2)
Includes (from E20)
- Note: All neoplasms, whether functionally active or not, are classified in Chapter 2. Appropriate codes in this chapter (i.e. E05.8, E07.0, E16-E31, E34.-) may be used as additional codes to indicate either functional activity by neoplasms and ectopic endocrine tissue or hyperfunction and hypofunction of endocrine glands associated with neoplasms and other conditions classified elsewhere.
Excludes1
Not coded here — never report together with this code.
- transitory endocrine and metabolic disorders specific to newborn (P70-P74) (from E20)
- galactorrhea (N64.3) (from E20)
- gynecomastia (N62) (from E20)
- Di George's syndrome (D82.1) (from E20)
- postprocedural hypoparathyroidism (E89.2) (from E20)
- tetany NOS (R29.0) (from E20)
- transitory neonatal hypoparathyroidism (P71.4) (from E20)
Code also
An additional code may be needed.
Also known as
- Autosomal dominant hypocalcemia type 1 (ADH1)
- Autosomal dominant hypocalcemia type 2 (ADH2)
- Hypocalcemia, autosomal dominant
- Hypocalcemia, autosomal dominant, type 1
- Hypocalcemia, autosomal dominant, type 2
Parent code
- E20.81Hypoparathyroidism due to impaired parathyroid hormone secretionHeader
Related codes
- E20.811Secondary hypoparathyroidism in diseases classified elsewhereBillable
- E20.812Autoimmune hypoparathyroidismBillable
- E20.818Other specified hypoparathyroidism due to impaired parathyroid hormone secretionBillable
- E20.819Hypoparathyroidism due to impaired parathyroid hormone secretion, unspecifiedBillable