Enchondromatosis

Enchondromatosis
Classification and external resources
Specialty	medical genetics
ICD-10	Q78.4
ICD-9-CM	756.4
DiseasesDB	9212
eMedicine	radio/247
MeSH	D004687

Enchondromatosis is a form of osteochondrodysplasia characterized by a proliferation of enchondromas.

Ollier disease can be considered a synonym for enchondromatosis.^[1] Maffucci syndrome is enchondromatosis with hemangiomatosis.^[2]

References

↑ "Ollier disease" at Dorland's Medical Dictionary
↑ Faik A, Allali F, El Hassani S, Hajjaj-Hassouni N (February 2006). "Maffucci's syndrome: a case report". Clin. Rheumatol. 25 (1): 88–91. doi:10.1007/s10067-005-1101-1. PMID 16234991.

Tumours of bone and cartilage (ICD-O 9180–9269) (C40–C41/D16, 170/213)

Diaphysis

Myeloid	Multiple myeloma

Epithelial	Adamantinoma

PNET/Ewing family	Ewing's sarcoma

Metaphysis

Osteoblast	Osteoid osteoma Osteoblastoma Osteoma/osteosarcoma

Chondroblast	Chondroma/ecchondroma/enchondroma Enchondromatosis Extraskeletal chondroma Chondrosarcoma Mesenchymal chondrosarcoma Myxoid chondrosarcoma Osteochondroma Osteochondromatosis Chondromyxoid fibroma

Fibrous	(Peripheral) Ossifying fibroma Fibrosarcoma

Epiphysis

Chondroblast	Chondroblastoma

Myeloid	Giant-cell tumor of bone

Other/ungrouped

Notochord	Chordoma

Osteochondrodysplasia (Q77–Q78, 756.4–756.5)

Osteodysplasia//
osteodystrophy

Diaphysis	Camurati–Engelmann disease

Metaphysis	Metaphyseal dysplasia Jansen's metaphyseal chondrodysplasia Schmid metaphyseal chondrodysplasia

Epiphysis	Spondyloepiphyseal dysplasia congenita Multiple epiphyseal dysplasia Otospondylomegaepiphyseal dysplasia

Osteosclerosis	Raine syndrome Osteopoikilosis Osteopetrosis

Other/ungrouped	FLNB Boomerang dysplasia Opsismodysplasia Polyostotic fibrous dysplasia McCune–Albright syndrome

Chondrodysplasia/
chondrodystrophy
(including dwarfism)

Osteochondroma

osteochondromatosis
- Hereditary multiple exostoses

Chondroma/enchondroma

enchondromatosis
- Ollier disease
- Maffucci syndrome

Growth factor receptor

FGFR2:	Antley–Bixler syndrome

FGFR3:	Achondroplasia Hypochondroplasia Thanatophoric dysplasia

COL2A1 collagen disease

SLC26A2 sulfation defect

Chondrodysplasia punctata

Other dwarfism

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