Concept information
...
Genetic disease
Hereditary disease
Autosomal hereditary disorder
Dominant hereditary disorder, NOS
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Congenital malformation
Congenital malformation syndrome (disorder)
Multiple system malformation syndrome
Multiple malformation syndrome with limb defect as major feature
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Congenital malformation
Congenital malformation syndrome (disorder)
Multiple system malformation syndrome
Multiple malformation syndrome with limb defect as major feature
...
Finding of limb structure
Upper extremity finding
Disease of upper extremity
Congenital anomaly of upper limb
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Finding of limb structure
Disease of extremity
Disease of upper extremity
Congenital anomaly of upper limb
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Finding of limb structure
Disease of extremity
Congenital anomaly of limb
Congenital anomaly of upper limb
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Congenital disease
Congenital malformation
Congenital anomaly of limb
Congenital anomaly of upper limb
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developmental disorder
Congenital malformation
Congenital anomaly of limb
Congenital anomaly of upper limb
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Disease of cardiovascular system
Heart disease
Structural disorder of heart
Congenital heart disease
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Disease of cardiovascular system
Heart disease
Structural disorder of heart
Congenital heart disease
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Congenital anomaly of trunk
Congenital anomaly of upper trunk
Congenital anomaly of thorax
Congenital heart disease
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Congenital anomaly of trunk
Congenital anomaly of upper trunk
Congenital anomaly of thorax
Congenital heart disease
...
Congenital malformation
Congenital anomaly of cardiovascular system
Congenital anomaly of cardiovascular structure of trunk
Congenital heart disease
...
Congenital malformation
Congenital anomaly of cardiovascular system
Congenital anomaly of cardiovascular structure of trunk
Congenital heart disease
...
Congenital malformation
Congenital anomaly of trunk
Congenital anomaly of cardiovascular structure of trunk
Congenital heart disease
Preferred term
Holt-Oram syndrome
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Associated morphology
Finding site
Is a
- 109420003
- 298756009
- 363005004
- 363212003
- 88631000119105
- Arrhythmia
- Congenital anomaly of upper limb
- Congenital heart disease
- Developmental hereditary disorder
- Dominant hereditary disorder, NOS
- Multiple malformation syndrome with limb defect as major feature
Occurrence
Pathological process
In other languages
-
Persian
URI
http://www.irandoc.acir/onto/irandoc/19092004
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