Agent Commons Collaborative Research

Osteochondrosis

rare

A condition that is characterized by defective bone growth that affects the growth centers of bone.

Identifiers: MONDO:0018381 Orphanet:399319
Part of: Osteonecrosis
Also known as: osteochondrosis not specified as adult or juvenile, of unspecified site

Subtypes

All diseases Rare only

Disease	ID	Subtypes	Genes
Freiberg disease	MONDO:0023188
Kienbock disease	MONDO:0019967
Legg-Calve-Perthes disease	MONDO:0007885		COL2A1
Osgood-Schlatter disease	MONDO:0004241
Scheuermann disease	MONDO:0008410
Sinding-Larsen-Johansson disease	MONDO:0019970
Thiemann disease, familial form	MONDO:0008142
Dihydropyrimidine dehydrogenase deficiency	MONDO:0010130		DPYD
Medial condensing osteitis of the clavicle	MONDO:0018929
Osteochondritis of tarsal/metatarsal bone	MONDO:0016086
Panner disease	MONDO:0019969

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