Camurati-Engelmann disease

Summary

Camurati-Engelmann disease is a developmental defect during embryogenesis^[1]. It draws 40 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #116 of 308).^[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's subclass of is recorded as osteosclerosis^[6].
• Camurati-Engelmann disease's subclass of is recorded as primary bone dysplasia with increased bone density^[7].
• Camurati-Engelmann disease's subclass of is recorded as monogenic disease^[8].
• Camurati-Engelmann disease's MeSH descriptor ID is recorded as D003966^[9].
• Camurati-Engelmann disease's OMIM ID is recorded as 606631^[10].
• Camurati-Engelmann disease's OMIM ID is recorded as 131300^[11].
• Camurati-Engelmann disease's ICD-9 ID is recorded as 756.59^[12].
• Camurati-Engelmann disease's DiseasesDB is recorded as 4301^[13].
• Camurati-Engelmann disease's Freebase ID is recorded as /m/03qkxbv^[14].
• Camurati-Engelmann disease's KEGG ID is recorded as H00434^[15].
• Camurati-Engelmann disease's GeneReviews ID is recorded as NBK1156^[16].
• Camurati-Engelmann disease's MeSH tree code is recorded as C05.116.099.708.180^[17].
• Camurati-Engelmann disease's MeSH tree code is recorded as C16.320.144^[18].
• Camurati-Engelmann disease's Disease Ontology ID is recorded as DOID:4997^[19].
• Camurati-Engelmann disease's Encyclopædia Britannica Online ID is recorded as science/progressive-diaphyseal-dysplasia^[20].
• Camurati-Engelmann disease's Orphanet ID is recorded as 1328^[21].
• Camurati-Engelmann disease's ICD-9-CM is recorded as 756.59^[22].
• Camurati-Engelmann disease's NCI Thesaurus ID is recorded as C84610^[23].
• Camurati-Engelmann disease's health specialty is recorded as medical genetics^[24].
• Camurati-Engelmann disease's genetic association is recorded as TGFB1^[25].
• Camurati-Engelmann disease's exact match is recorded as http://purl.obolibrary.org/obo/DOID_4997^[26].
• Camurati-Engelmann disease's exact match is recorded as http://identifiers.org/doid/DOID:4997^[27].

Why It Matters

Camurati-Engelmann disease draws 40 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #116 of 308).^[2] It has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.^[28] It is known by 27 alternative names across languages and contexts.^[29]