Holt-Oram syndrome
autosomal dominant disease characterized by congenital anomalies located_in heart and located_in upper limb.
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Holt-Oram syndrome
Summary
Holt-Oram syndrome is a developmental defect during embryogenesis[1]. It draws 54 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's subclass of is recorded as autosomal dominant disease[8].
- Holt-Oram syndrome's subclass of is recorded as atriodigital dysplasia[9].
- Holt-Oram syndrome's subclass of is recorded as multiple congenital anomalies/dysmorphic syndrome without intellectual disability[10].
- Holt-Oram syndrome's subclass of is recorded as genetic cardiac rhythm disease[11].
- Holt-Oram syndrome's subclass of is recorded as rare syndrome with cardiac malformations[12].
- Holt-Oram syndrome's MeSH descriptor ID is recorded as C535326[13].
- Holt-Oram syndrome's OMIM ID is recorded as 142900[14].
- Holt-Oram syndrome's DiseasesDB is recorded as 5988[15].
- Holt-Oram syndrome's Freebase ID is recorded as /m/0dlqkh[16].
- Holt-Oram syndrome's KEGG ID is recorded as H00433[17].
- Holt-Oram syndrome's GeneReviews ID is recorded as NBK1111[18].
- Holt-Oram syndrome's eMedicine ID is recorded as 159911[19].
- Holt-Oram syndrome's Disease Ontology ID is recorded as DOID:0060468[20].
- Holt-Oram syndrome's Orphanet ID is recorded as 392[21].
- Holt-Oram syndrome's ICD-9-CM is recorded as 759.89[22].
- Holt-Oram syndrome's NCI Thesaurus ID is recorded as C125592[23].
- Holt-Oram syndrome's health specialty is recorded as medical genetics[24].
- Holt-Oram syndrome's genetic association is recorded as TBX5[25].
- Holt-Oram syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060468[26].
- Holt-Oram syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060468[27].
Why It Matters
Holt-Oram syndrome draws 54 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.[28] It is known by 13 alternative names across languages and contexts.[29]