Chapter 17 - Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)»Chromosomal abnormalities, not elsewhere classified (Q90-Q99)»Trisomy 13, unspecified (Q91.7)
Q91.7
Trisomy 13, unspecified
Related indications (MeSH) (1)
A chromosome disorder associated with TRISOMY of all or part of CHROMOSOME 13. Clinical manifestations include CONGENITAL HEART DEFECTS (e.g., PATENT DUCTUS ARTERIOSUS), facial malformations (e.g., CLEFT LIP; CLEFT PALATE; COLOBOMA; MICROPHTHALMIA); HYPOTONIA, digit malformations (e.g., POLYDACTYLY or SYNDACTYLY), and SEIZURES and severe INTELLECTUAL DISABILITY associated with NERVOUS SYSTEM MALFORMATIONS.