Holt-Oram syndrome
autosomal dominant disease characterized by congenital anomalies located_in heart and located_in upper limb.
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Summary
Holt-Oram syndrome is a developmental defect during embryogenesis[1]. It draws 187 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #91 of 308).[2]
Key Facts
- Holt-Oram syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Holt-Oram syndrome's instance of is recorded as rare disease[4].
- Holt-Oram syndrome's instance of is recorded as class of disease[5].
- Mary Holt is named after Holt-Oram syndrome[6].
- Samuel Oram is named after Holt-Oram syndrome[7].
- Holt-Oram syndrome is a type of autosomal dominant disease[8].
- Holt-Oram syndrome is a type of atriodigital dysplasia[9].
- Holt-Oram syndrome is a type of multiple congenital anomalies/dysmorphic syndrome without intellectual disability[10].
- Holt-Oram syndrome is a type of genetic cardiac rhythm disease[11].
- Holt-Oram syndrome is a type of rare syndrome with cardiac malformations[12].
- Holt-Oram syndrome's ICD-9-CM is recorded as 759.89[13].
- Holt-Oram syndrome's NCI Thesaurus ID is recorded as C125592[14].
- Holt-Oram syndrome's health specialty is recorded as medical genetics[15].
- Holt-Oram syndrome's genetic association is recorded as TBX5[16].
- Holt-Oram syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060468[17].
- Holt-Oram syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060468[18].
- Holt-Oram syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_392[19].
- Holt-Oram syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[20].
Why It Matters
Holt-Oram syndrome draws 187 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #91 of 308).[2] It has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[21] It is known by 13 alternative names across languages and contexts.[22]