ICD-11 classes
12 Diseases of the respiratory system
Respiratory diseases principally affecting the lung...
CB05 — Interstitial lung diseases associated with systemic diseases
CB05.3 — Interstitial lung diseases associated with metabolic...
5A51.2 — Familial hypocalciuric hypercalcaemia
ICD-11 5A51.2 — Familial hypocalciuric hypercalcaemia
Familial Hypocalciuric Hypercalcaemia (FHH) or benign familial hypercalcaemia is an autosomal dominant disorder of calcium metabolism that is often asymptomatic and that is biologically characterised by a significant but moderate hypercalcaemia. Serum levels of parathyroid hormone are normal or slightly increased, and urinary calcium excretion is relatively low for hypercalcaemia. CASR, GNA11 and AP2S1 have been identified as causative genes.
The diagnosis includes nothing.
The diagnosis excludes nothing.
It has no clarifying diagnoses.
The diagnosis is coded elsewhere:
- Hyperparathyroidism #4329
- Disorders of calcium metabolism #5019
- Renal hypocalciuria #19692