Autosomal dominant hypocalcemia
- E20.810 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- ICD-10-CM E20.810 is a new 2024 ICD-10-CM code that became effective on October 1, 2023.
- This is the American ICD-10-CM version of E20.810 – other international versions of ICD-10 E20.810 may differ.
Applicable To
- Autosomal dominant hypocalcemia type 1 (ADH1)
- Autosomal dominant hypocalcemia type 2 (ADH2)
Code Also
- , if applicable, any associated conditions, such as:
- calculus of kidney (N20.0)
- chronic kidney disease (N18.-)
- respiratory distress (J80, R06.-)
- seizure disorder (G40.-, R56.9)
The following code(s) above E20.810 contain annotation back-references
that may be applicable to E20.810:
- E00-E89 Endocrine, nutritional and metabolic diseases
- E20-E35 Disorders of other endocrine glands
- E20 Hypoparathyroidism
ICD-10-CM E20.810 is grouped within Diagnostic Related Group(s) (MS-DRG v41.0):
- 643 Endocrine disorders with mcc
- 644 Endocrine disorders with cc
- 645 Endocrine disorders without cc/mcc
- 791 Prematurity with major problems
- 793 Full term neonate with major problems
Code History
- 2024 (effective 10/1/2023): New code
Code annotations containing back-references to E20.810:
- Type 1 Excludes: E83.5
Diagnosis Index entries containing back-references to E20.810:
- HypocalcemiaE83.51
- autosomal dominant E20.810
- type 1 E20.810 (ADH1)
- type 2 E20.810 (ADH2)
- autosomal dominant E20.810