Familial tumoral calcinosis

MONDO:0018891

Tumoral calcinosis is a phosphocalcic metabolism anomaly, particularly among younger age groups and characterized by the presence of calcified masses in the juxta-articular regions (hip, elbow, ankle and scapula) without joint involvement. Histologically, lesions dysplay collagen necrobiosis, followed by cyst formation and a foreign-body response with calcification Two forms of tumoral calcinosis have been described: normocalcemic tumoral calcinosis and familial tumoral calcinosis.

1428 clinical trials for this condition and its sub-types, 1 tagged with Familial tumoral calcinosis itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Integumentary system disorder (4553) ↑ Endocrine gland neoplasm (3332) ↑ Calcinosis (47)

Sub-types of Familial tumoral calcinosis

Familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome 0 trials
Normophosphatemic familial tumoral calcinosis 0 trials
Tumoral calcinosis, hyperphosphatemic, familial, 1 0 trials
Tumoral calcinosis, hyperphosphatemic, familial, 2 0 trials
Tumoral calcinosis, hyperphosphatemic, familial, 3 0 trials

Including sub-types (1428) Tagged with Familial tumoral calcinosis (1)

Trials to join now! 1

NIH launches major study to unlock secrets of rare bone diseases

Knowledge-focused Recruiting now

This study aims to collect information and bone samples from up to 1,000 people with bone or mineral disorders, such as tumor-induced osteomalacia or familial tumoral calcinosis. Participants receive standard medical evaluations and may provide bone tissue from surgery or a biops…

Sponsor: National Institute of Dental and Craniofacial Research (NIDCR) • Aim: Knowledge-focused

Last updated Sep 18, 2026 00:00 UTC

Familial tumoral calcinosis

Where it sits in the disease tree

NIH launches major study to unlock secrets of rare bone diseases