congenital rubella syndrome
human disease
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Summary
congenital rubella syndrome is a developmental defect during embryogenesis[1]. It has Wikipedia articles in 15 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- congenital rubella syndrome is credited with the discovery of Norman Gregg[3].
- congenital rubella syndrome's instance of is recorded as developmental defect during embryogenesis[4].
- congenital rubella syndrome's instance of is recorded as infectious disease[5].
- congenital rubella syndrome's instance of is recorded as class of disease[6].
- congenital rubella syndrome is a type of congenital transmission[7].
- congenital rubella syndrome is a type of infectious embryofetopathy[8].
- congenital rubella syndrome is a type of infectious disease with epilepsy[9].
- congenital rubella syndrome is a type of rubella virus infectious disease[10].
- congenital rubella syndrome's Commons category is recorded as Congenital rubella syndrome[11].
- congenital rubella syndrome's has cause is recorded as rubella[12].
- congenital rubella syndrome's ICD-9-CM is recorded as 771.0[13].
- congenital rubella syndrome's NCI Thesaurus ID is recorded as C34992[14].
- congenital rubella syndrome's health specialty is recorded as pediatrics[15].
- congenital rubella syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_9228[16].
- congenital rubella syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_290[17].
- congenital rubella syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].
Body
Works and Contributions
congenital rubella syndrome is credited with the discovery of Norman Gregg[3].
Why It Matters
congenital rubella syndrome has Wikipedia articles in 15 language editions, a strong signal of global cultural recognition.[2] It is known by 18 alternative names across languages and contexts.[19]