Caffey disease
bone inflammation disease in infants
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Caffey disease
Summary
Caffey disease is a developmental defect during embryogenesis[1]. It draws 25 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #129 of 308).[2]
Key Facts
- Caffey disease's instance of is recorded as developmental defect during embryogenesis[3].
- Caffey disease's instance of is recorded as rare disease[4].
- Caffey disease's instance of is recorded as class of disease[5].
- Caffey disease is a type of bone inflammation disease[6].
- Caffey disease is a type of neonatal osteosclerotic dysplasia[7].
- Caffey disease is a type of cortical hyperostosis[8].
- Caffey disease's Commons category is recorded as Infantile cortical hyperostosis[9].
- Caffey disease's symptoms and signs is recorded as irritability[10].
- Caffey disease's ICD-9-CM is recorded as 756.59[11].
- Caffey disease's NCI Thesaurus ID is recorded as C118423[12].
- Caffey disease's NCI Thesaurus ID is recorded as C84645[13].
- Caffey disease's health specialty is recorded as rheumatology[14].
- Caffey disease's genetic association is recorded as COL1A1[15].
- Caffey disease's exact match is recorded as http://purl.obolibrary.org/obo/DOID_4257[16].
- Caffey disease's exact match is recorded as http://identifiers.org/doid/DOID:4257[17].
- Caffey disease's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1310[18].
- Caffey disease's on focus list of Wikimedia project is recorded as WikiProject Medicine[19].
Why It Matters
Caffey disease draws 25 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #129 of 308).[2] It has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[20] It is known by 9 alternative names across languages and contexts.[21]