"Trisomy 13 Syndrome" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
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.
| Descriptor ID |
D000073839
|
| MeSH Number(s) |
C10.597.606.643.835 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
|
| Concept/Terms |
Trisomy 13 Syndrome- Trisomy 13 Syndrome
- Patau's Syndrome
- Pataus Syndrome
- Bartholin-Patau Syndrome
- Bartholin Patau Syndrome
- Chromosome 13 Trisomy Syndrome
- Trisomy 13 Syndromes
- Patau Syndrome
|
Below are MeSH descriptors whose meaning is more general than "Trisomy 13 Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Trisomy 13 Syndrome".
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Below are the most recent publications written about "Trisomy 13 Syndrome" by people in Profiles.