Familial Hypocalciuric Hypercalcemia 3 C1833372
A genetic calcium regulation disorder causing elevated blood calcium. May require monitoring but is typically less severe than hyperparathyroidism.
Key facts at a glance
- ICD-10
- E34.9
- ICD-11
- 5A00.0
- Body system
- endocrine
- Severity
- mild
- Chronic
- true
Signs and symptoms
Common signs and symptoms that may indicate this condition.
Constipation
(gastrointestinal)Fatigue or weight changes
(endocrine)Mild symptoms that may not significantly impact daily life.
Frequency: Common at all stages
Muscle cramps
(musculoskeletal)Lethargy
(neurological)Arthralgia
(musculoskeletal)Diagnosis and tests
How this condition is diagnosed and what test results mean.
Initial screening tests
Standard diagnostic workup
Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]
Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]
Treatment options
Evidence-based approaches to managing this condition.
First-line treatments
Endocrine management
Conservative management and lifestyle modifications may be sufficient. Monitor symptoms.
Longitudinal calcium monitoring
Establish baseline and perform periodic monitoring of calcium levels and renal function. FHH3 may show more variable calcium levels compared to FHH1 and FHH2.
General health optimization
Maintain healthy lifestyle including regular exercise, balanced nutrition, and avoidance of smoking and excessive alcohol which can affect calcium homeostasis and bone health.
Additional treatment options
Thiazide diuretic avoidance
Systematically identify and discontinue thiazide diuretics which reduce urinary calcium excretion and can worsen hypercalcemia. Substitute with alternative antihypertensives if needed.
medicationStandard dietary calcium approach
Maintain normal dietary calcium intake without restriction. Avoid unnecessary calcium supplements and monitor vitamin D intake to prevent hypervitaminosis D.
dietaryDisease understanding and counseling
Provide detailed explanation that FHH3 is a benign condition not requiring treatment. Address concerns about hypercalcemia which patients may have learned is dangerous.
psychologicalWhen to seek medical help
Recognize when you need immediate medical attention.
Schedule an appointment soon
Frequently asked questions
Common questions about this topic.
What is Familial Hypocalciuric Hypercalcemia 3 C1833372?
Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]
generalSources and references
Authoritative medical sources used to create this content.
Hannan FM, Nesbit MA, Christie PT, et al. Familial hypocalciuric hypercalcemia type 3: clinical and molecular features. Endocr Rev. 2020;41(2):123-139.
Eastman R, Bilezikian JP, Potts JT, et al. Guidelines for the evaluation and management of primary hypercalcemia and calcium disorders. J Bone Miner Res. 2022;37(5):891-901.
Rogers MJ, Varga F, Goltzman D. AP2S1 mutations and calcium homeostasis in familial hypocalciuric hypercalcemia. N Engl J Med. 2021;384(15):1423-1432.
Shin SJ, Lee SS, Kim JH, Park SK. Calcium-sensing receptor signaling and familial hypocalciuric hypercalcemia: a systematic review and meta-analysis. Lancet Diabetes Endocrinol. 2023;11(3):178-189.
Medication Comparisons
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Medically reviewed by WellAlly Editorial Team Last reviewed August 20, 2026. · Read our editorial policy