Concept information
اصطلاح مرجح
Congenital malformation
نوع
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
مفهوم اعم
مفهومهای اخص
- 11p15 duplication syndrome (disorder)
- 12q15q21.1 microdeletion syndrome (disorder)
- 16q24.1 microdeletion syndrome (disorder)
- 17q24-qter duplication syndrome
- 1p21.3 microdeletion syndrome (disorder)
- 2q24 microdeletion syndrome (disorder)
- 3p25.3 deletion syndrome (disorder)
- 9p24.3 deletion syndrome (disorder)
- Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder)
- Bowen-Conradi syndrome (disorder)
- Chromosome 1q21.1 deletion syndrome
- Chromosome Xp11.3 microdeletion syndrome (disorder)
- Complete trisomy 18 syndrome
- Complete trisomy 21 syndrome
- Congenital anomaly of head
- Congenital anomaly of limb
- Congenital anomaly of mother complicating pregnancy (disorder)
- Congenital anomaly of musculoskeletal system
- Congenital anomaly of neck
- Congenital deformity
- Congenital ectodermal defect
- Congenital hemihypertrophy
- Congenital malformation syndrome (disorder)
- Conjoined twins
- Cyst of paramesonephric duct (disorder)
- Distal 16p11.2 microdeletion syndrome
- Distal monosomy 1p36
- Distal trisomy 20q
- Distal trisomy 7p (disorder)
- Distal trisomy 7q11.23
- Distal Xq28 microduplication syndrome
- Embryonic cyst of Gartner's duct
- FRAXE intellectual disability syndrome (disorder)
- FRAXF syndrome (disorder)
- Gynandromorphism syndrome
- Isodicentric chromosome 15 syndrome (disorder)
- Lymphatic malformation
- Monosomy 7q31
- Mosaic trisomy 10 syndrome (disorder)
- Mullerian aplasia
- Nicolaides-Baraitser syndrome (disorder)
- Oculootodental syndrome
- Single congenital anomaly
- Situs ambiguus
- Telomeric deletion 7p
مورفولوژی مرتبط
وقوع
فرآیند پاتولوژیک
در زبان های دیگر
-
Persian
URI
http://www.irandoc.acir/onto/irandoc/276654001
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