genochondromatosis type 2
MONDO:0019680Mondo
Findings
No curated finding names genochondromatosis type 2 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Genochondromatosis type 2 is a rare genetic bone development disorder characterized by normal clavicles and symmetrical generalized metaphyseal enchondromas particularly in the distal femur, proximal humerus, and bones of the wrists, hands, and feet. Lesions regress later in life with growth cartilage obliteration. Clinical examination is normal and the course of the disease is benign.
Definition from the Mondo Disease Ontology (MONDO:0019680), read 2026-09-29. CC BY 4.0.
Where it sits
- A kind of