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Hypoparathyroidism is described in the MONDO definition as an endocrine disorder in which the parathyroid glands in the neck do not produce enough parathyroid hormone (PTH). Disease subtypes listed in the packet are autoimmune hypoparathyroidism, secondary hypoparathyroidism due to impaired parathormone secretion, and hereditary hypoparathyroidism. Prevalence estimates are not certified in this packet.
According to the MONDO definition, common signs and symptoms include abdominal pain, brittle nails, cataracts, dry hair and skin, muscle cramps, tetany, pain in the face, legs, and feet, seizures, tingling sensation, and weakened tooth enamel in children. Structured phenotype annotations, frequency data, and age-of-onset categories are not populated in this packet.
The MONDO definition states that hypoparathyroidism may be caused by injury to the parathyroid glands, for example during surgery. Other causes named in the definition include low blood magnesium levels, a side effect of radioactive iodine treatment for hyperthyroidism, metabolic alkalosis, DiGeorge syndrome, and type I polyglandular autoimmune syndrome. The packet lists no associated genes and no inheritance patterns, so a genetic basis and mode of inheritance are not certified here, although one listed subtype is named hereditary hypoparathyroidism.
Diagnostic methods, criteria, and newborn screening information are not certified in this packet.
The MONDO definition states that the goal of treatment is to restore the calcium and mineral balance in the body. The packet's FDA-approved treatment records list three products with market status ACTIVE: Yorvipath (palopegteriparatide, NDA, approved 2024-08-09), Natpara (parathyroid hormone, BLA, approved 2015-01-23), and Drisdol (ergocalciferol, NDA, approved 1941-01-11). Orphan drug records list Yorvipath and Natpara with an indication of treatment of hypoparathyroidism. Several other agents appear in orphan drug records with status DESIGNATED, and one synthetic human parathyroid hormone 1-34 record has status WITHDRAWN; orphan designation does not indicate approval or availability, and these entries are not current approved options. Supportive care approaches are not certified in this packet.
38 trials found
Prognosis and natural history are not certified in this packet.
The packet reports ClinicalTrials.gov records for hypoparathyroidism. Examples include NCT07081997, a phase 3 trial of palopegteriparatide in adults sponsored by Ascendis Pharma Bone Diseases A/S (recruiting, start 2026-05-07); NCT07699471, a phase 3 study of canvuparatide versus placebo in adults sponsored by MBX Biosciences (recruiting, start 2026-08-26), and NCT07857460, the German Hypoparathyroidism Registry sponsored by University Hospital Augsburg (recruiting, start 2021-07-06). The packet also lists the patient organization Hypoparathyroidism Association (hypopara.org).
Data assembled from 4 of 12 sources · Last updated Nov 2, 2026, 8:17 PM UTC
Patient Advocacy Groups (PAGs) provide support, resources, and community for patients and caregivers.
Genetic and Rare Diseases Info Center
AI-curated news mentioning hypoparathyroidism
Updated Oct 12, 2026
A recent cross-sectional online survey highlights the medical and psychosocial challenges faced by patients with hypoparathyroidism in China. The findings underscore the need for improved patient support and management strategies.
A recent study identifies pathogenic variants of the GATA3 gene as the cause of hypomagnesemia in patients with hypoparathyroidism, sensorineural deafness, and renal dysplasia syndrome. This discovery enhances understanding of the genetic underpinnings of these rare conditions.
A joint meeting of experts focused on hypoparathyroidism has resulted in a resolution addressing the challenges and technological advancements in managing the condition. This gathering highlights the ongoing efforts to improve understanding and treatment options for hypoparathyroidism.