Concept information
اصطلاح مرجح
Congenital malformation
نوع
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http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
مفهوم اعم
مفهومهای اخص
- 13q partial monosomy syndrome
- 15q11q13 microduplication syndrome (disorder)
- 15q13.3 deletion syndrome
- 15q13.3 microduplication syndrome (disorder)
- 16p11.2p12.2 microduplication syndrome
- 16p13.11 microduplication syndrome (disorder)
- 16q24.3 microdeletion syndrome (disorder)
- 17q11 deletion syndrome (disorder)
- 17q23.1-q23.2 duplication syndrome
- 20p12.2 deletion syndrome (disorder)
- 7p12-p14 deletion syndrome
- 7p21.1 deletion syndrome
- 9q34 deletion syndrome (disorder)
- Cat eye syndrome
- Chromosome 16p11.2 deletion syndrome
- Chromosome 2q37 deletion syndrome
- Complete trisomy 22 syndrome
- Congenital anomaly of craniovertebral junction (disorder)
- Congenital anomaly of limb
- Congenital malformation caused by valproic acid
- Congenital malformation of lymphatic system of cervicofacial region (disorder)
- Congenital malformation syndrome (disorder)
- Conjoined twins
- Distal 7q11.23 microdeletion syndrome (disorder)
- Distal monosomy 12p
- Dysmorphism
- Hereditary ovalocytosis
- Monosomy 15q11.2
- Peripheral myelin protein 22-retinoic acid induced 1 contiguous gene duplication syndrome (disorder)
- Phelan-McDermid syndrome
- Proximal 16p11.2 microdeletion syndrome (disorder)
- Proximal 16p11.2 microduplication syndrome (disorder)
- Retinitis pigmentosa-deafness syndrome
- Spinal dysraphism
مورفولوژی مرتبط
وقوع
فرآیند پاتولوژیک
در زبان های دیگر
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Persian
URI
http://www.irandoc.acir/onto/irandoc/276654001
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