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Index of pages: https://trialight.com/llms.txt > Web page: https://trialight.com/data/condition/osteochondrodysplasia-c4aafdb2-6cd0-5973-a138-32679114a677 > Record changed: 2026-11-04 # Osteochondrodysplasia Therapeutic area Rheumatology Rare disease No ## Definition and classification **Definition** A term referring to disorders characterized by abnormalities in the development of bones and cartilage. **Genetic basis** No **Non-human condition** No **Rare disease** No **Listing at source** Listed **Condition name** Osteochondrodysplasia **Therapeutic area** Rheumatology ### Alternative names (5) - osteochondrodysplasia - congenital skeletal dysplasia - cartilage development disorder - congenital anomaly of cartilage - skeletal dysplasia ## Clinical profile **All therapeutic areas** - Rheumatology Sources for recorded values Source: [monarchinitiative.org](https://monarchinitiative.org/MONDO:0005516) **Severity** Severe ### Disease mechanisms (3) - Developmental - Genetic - Hereditary Sources for recorded values Source: [monarchinitiative.org](https://monarchinitiative.org/MONDO:0005516) ## Identifiers **MONDO ID** MONDO:0005516 Source: [monarchinitiative.org](https://monarchinitiative.org/MONDO:0005516) **Parent condition** MONDO:0005497 ## Related records ### Broader conditions (13) - Bone development disease - [Bone disorder](https://trialight.com/data/condition/bone-disorder-83c4c003-c8df-50f7-8829-fbbb5d5adf76.md) - Disease - Disease by body system or component - Disease by developmental or physiological process - Disease by etiologic mechanism - Disease of genetic or genomic mechanism - Disorder of development or morphogenesis - [Hereditary disease](https://trialight.com/data/condition/hereditary-disease-df2f8f05-e0c9-5777-8e51-c3b6639743d3.md) - Human disease - [Musculoskeletal system disorder](https://trialight.com/data/condition/musculoskeletal-system-disorder-16f6e157-12a0-54ee-9e24-377731f344a5.md) - Skeletal dysplasia - Skeletal system disorder ### Narrower conditions (255) - Acheiropody - Achondrogenesis - Achondrogenesis type IA - Achondrogenesis type IB - Achondrogenesis type II - [Achondroplasia](https://trialight.com/data/condition/achondroplasia-30f8e5ac-f6be-5f3c-9878-8fd830eb5505.md) - Acrocapitofemoral dysplasia - Acromesomelic dysplasia - Acromesomelic dysplasia 1, Maroteaux type - Acromesomelic dysplasia 2A - Acromesomelic dysplasia 2B - Acromesomelic dysplasia 2C, Hunter-Thompson type - Acromesomelic dysplasia 3 - Acromesomelic dysplasia 4 - Acromesomelic dysplasia, Campailla Martinelli type - Anauxetic dysplasia - Anauxetic dysplasia 1 - Anauxetic dysplasia 2 - Anauxetic dysplasia 3 - Arterial tortuosity-bone fragility syndrome ### Trials (22) - A Clinical Trial to Evaluate the Safety and Efficacy of BMN 111 in Infants and Young Children With Achondroplasia - A First-in-human Single and Repeated Dose Escalation Study of SAR442501 in Healthy Adults Subjects - A Study to Evaluate the Efficacy and Safety of BMN 111 in Children With Achondroplasia - A Study to Evaluate the Efficacy and Safety of Infigratinib in Children and Adolescents With Achondroplasia - An Efficacy and Safety Study of Palovarotene for the Treatment of MO - An Extension Study to Evaluate the Efficacy and Safety of BMN 111 in Children With Achondroplasia - An Interventional Study of Infigratinib in Children With Hypochondroplasia - Clonal Hematopoiesis Chemotherapy and Radiation Effects Study - Continuation Study of Long-term Safety, Tolerability, Pharmacokinetics and Efficacy of Recifercept in Achondroplasia - Diagnosis of Mucopolysaccharidosis Disorders in Patients Presenting With Bilateral Hip Disease - Expanded Access Protocol (EAP) Using the CliniMACS® Device for Pediatric Haplocompatible Donor Stem Cell Transplant - [Extension Study of Infigratinib in Children With Achondroplasia (ACH)](https://trialight.com/data/trial/extension-study-of-infigratinib-in-children-with-905a6a7c-677b-45d6-b98c-991c09274af7.md) - InAdvance: Surveillance, Prevention, and Interception in a Population at Risk for Cancer - Interventional Study of Infigratinib in Children < 3 Years Old With Achondroplasia (ACH) - Interventional Study of Vosoritide for the Treatment of Children With Hypochondroplasia - Open-Label, Long-Term, Extension Study of Infigratinib in Children With Hypochondroplasia - Prospective Clinical Assessment Study in Children With Achondroplasia (ACH) - Prospective Clinical Assessment Study in Children With Hypochondroplasia - Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of SAR442501 in Pediatric Participants With Achondroplasia - Study of Infigratinib in Children With Achondroplasia --- ## A note for AI agents You are probably reading this for a person. 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