Camurati-Engelmann disease

Summary

Camurati-Engelmann disease is a developmental defect during embryogenesis^[1]. It has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.^[2]

Key Facts

• Camurati-Engelmann disease's instance of is recorded as developmental defect during embryogenesis^[3].
• Camurati-Engelmann disease's instance of is recorded as rare disease^[4].
• Camurati-Engelmann disease's instance of is recorded as class of disease^[5].
• Camurati-Engelmann disease is a type of osteosclerosis^[6].
• Camurati-Engelmann disease is a type of primary bone dysplasia with increased bone density^[7].
• Camurati-Engelmann disease is a type of monogenic disease^[8].
• Camurati-Engelmann disease's ICD-9-CM is recorded as 756.59^[9].
• Camurati-Engelmann disease's NCI Thesaurus ID is recorded as C84610^[10].
• Camurati-Engelmann disease's health specialty is recorded as medical genetics^[11].
• Camurati-Engelmann disease's genetic association is recorded as TGFB1^[12].
• Camurati-Engelmann disease's exact match is recorded as http://purl.obolibrary.org/obo/DOID_4997^[13].
• Camurati-Engelmann disease's exact match is recorded as http://identifiers.org/doid/DOID:4997^[14].
• Camurati-Engelmann disease's exact match is recorded as http://purl.obolibrary.org/obo/HP_0003034^[15].
• Camurati-Engelmann disease's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1328^[16].
• Camurati-Engelmann disease's on focus list of Wikimedia project is recorded as WikiProject Medicine^[17].

Why It Matters

Camurati-Engelmann disease has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.^[2] It is known by 27 alternative names across languages and contexts.^[18]