 E20.81 |
|
Hypoparathyroidism due to impaired parathyroid hormone secretion |
| |
 E20.810 |
 |
Autosomal dominant hypocalcemia |
| |
| Autosomal dominant hypocalcemia type 1 (ADH1) | | Autosomal dominant hypocalcemia type 2 (ADH2) |
| CodeAlso |
, 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)
|
|
|
| |
| E20.811 |
|
Secondary hypoparathyroidism in diseases classified elsewhere |
| |
| CodeFirst |
underlying condition, if known
|
|
|
| |
| E20.812 |
|
Autoimmune hypoparathyroidism |
| |
| CodeFirst |
, if applicable, underlying condition such as:
autoimmune polyglandular failure (E31.0)
Schmidt's syndrome (E31.0)
|
|
|
| |
| E20.818 |
|
Other specified hypoparathyroidism due to impaired parathyroid hormone secretion |
| |
| Familial isolated hypoparathyroidism |
|
|
| |
| E20.819 |
|
Hypoparathyroidism due to impaired parathyroid hormone secretion, unspecified |
|
