metachondromatosis
a rare disorder characterized by the presence of both multiple enchondromas and osteochondroma-like lesions
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metachondromatosis
Summary
metachondromatosis is a developmental defect during embryogenesis[1]. metachondromatosis has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- metachondromatosis's instance of is recorded as developmental defect during embryogenesis[3].
- metachondromatosis's instance of is recorded as rare disease[4].
- metachondromatosis's instance of is recorded as class of disease[5].
- metachondromatosis is a type of osteochondroma[6].
- metachondromatosis is a type of Enchondroma[7].
- metachondromatosis is a type of primary bone dysplasia with disorganized development of skeletal components[8].
- metachondromatosis is a type of autosomal dominant disease[9].
- metachondromatosis is a type of osteochondrodysplasia[10].
- metachondromatosis's ICD-9-CM is recorded as 756.59[11].
- metachondromatosis's genetic association is recorded as PTPN11[12].
- metachondromatosis's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2499[13].
- metachondromatosis's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111512[14].
- metachondromatosis's exact match is recorded as http://identifiers.org/doid/DOID:0111512[15].
Why It Matters
metachondromatosis has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[2] metachondromatosis is known by 3 alternative names across languages and contexts.[16]