Holt-Oram syndrome is an autosomal dominant disorder that affects the bones of the arms and hands, the upper limbs, and often causes heart problems as well. It is also called atrio-digital syndrome, atriodigital dysplasia, cardiac-limb syndrome, heart-hand syndrome type 1, ventriculo-radial syndrome and by the initials HOS. The syndrome may include an absent radial bone in the forearm, an atrial septal defect, which is an opening in the wall between the upper chambers of the heart, or heart block, a disturbance in the conduction of the heartbeat. It affects approximately one in 100,000 people. The many alternative names show how the condition has been described from both a cardiac and a limb point of view, and they all refer to the same combination of upper limb and heart findings.
Facts
Classification
ICD-10 ChapterXVII: Congenital Malformations, Deformations and Chromosomal Abnormalities 2 Communicable or Non-communicable Transmission Route Causative Agent
Causative Agent (category) Prevalence Band Sources
1. Holt-Oram syndrome (Wikipedia)
Lead section
is an autosomal dominant disorder
Lead section [body-system]
affects bones in the arms and hands
Lead section [body-system 2]
often causes heart problems
View the Source2. EMBL-EBI Ontology Lookup Service: Holt-Oram syndrome (DOID term)
EMBL-EBI Ontology Lookup Servicedatabase_cross_reference of the DOID term Holt-Oram syndrome; ICD-10 chapter derived from code Q87.2 (WHO range Q00-Q99)Quote, database_cross_reference of the DOID term Holt-Oram syndrome; ICD-10 chapter derived from code Q87.2 (WHO range Q00-Q99)
ICD10CM:Q87.2
View the Source 3. MedlinePlus Genetics (U.S. National Library of Medicine): Holt-Oram syndrome - MedlinePlus Genetics
MedlinePlus Genetics (U.S. National Library of Medicine)Description and InheritanceQuote, Description and Inheritance
Mutations in the TBX5 gene cause Holt-Oram syndrome.
View the Source 4. Orphadata (Orphanet): Orphadata epidemiology, ORPHAcode 392
Orphadata (Orphanet)Orphanet epidemiology, ORPHAcode 392Quote, Orphanet epidemiology, ORPHAcode 392
"PrevalenceClass": "1-9 / 1 000 000", "PrevalenceGeographic": "Europe", "PrevalenceQualification": "Value and class", "PrevalenceType": "Prevalence at birth"
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