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Trisomy 13 Syndrome MeSH Descriptor Data 2022


MeSH Heading
Trisomy 13 Syndrome
Tree Number(s)
C10.597.606.360.835
C14.240.400.970
C14.280.400.970
C16.131.077.919
C16.131.240.400.965
C16.131.260.923
C16.320.180.923
Unique ID
D000073839
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D000073839
Scope Note
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.
Entry Term(s)
Bartholin-Patau Syndrome
Chromosome 13 Duplication
Chromosome 13 Trisomy Syndrome
Complete Trisomy 13 Syndrome
Mosaic Trisomy 13 Syndrome
Patau Syndrome
Patau's Syndrome
Trisomy 13
Trisomy 13 Syndromes
Public MeSH Note
2018; TRISOMY 13 SYNDROME was indexed under TRISOMY; CHROMOSOMES, HUMAN, PAIR 13; and CHROMOSOME DISORDERS 2010-2017
History Note
2018(2010)
Date Established
2018/01/01
Date of Entry
2017/07/11
Revision Date
2019/07/01
Trisomy 13 Syndrome Preferred
Chromosome 13 Duplication Narrower
Complete Trisomy 13 Syndrome Narrower
Mosaic Trisomy 13 Syndrome Narrower
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