| Descriptor English: | Trisomy 18 Syndrome | ||||||
| Descriptor Spanish: |
Síndrome de la Trisomía 18
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| Descriptor Portuguese: | Síndrome da Trissomía do Cromossomo 18 | ||||||
| Descriptor French: | Syndrome d'Edwards | ||||||
| Entry term(s): |
Complete Trisomy 18 Syndrome Edwards Syndrome Mosaic Trisomy 18 Syndrome Trisomy 18 Trisomy 18 Syndromes Trisomy E Syndrome |
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| Tree number(s): |
C14.240.400.975 C14.280.400.975 C16.131.077.929 C16.131.240.400.968 C16.131.260.932 C16.320.180.932 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D000073842 | ||||||
| Scope note: | A chromosome disorder associated with TRISOMY of all or part of CHROMOSOME 18. Clinical manifestations include INTRAUTERINE GROWTH RETARDATION; CLEFT PALATE; CONGENITAL HEART DEFECTS; MICROCEPHALY; MICROGNATHIA and clenched fists with overlapping fingers. Most affected fetuses do not survive to birth. Those who survive through their first year often have severe INTELLECTUAL DISABILITY. |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Public MeSH Note: | 2018; TRISOMY 18 was indexed under CHROMOSOMES, HUMAN, PAIR 18; and TRISOMY 2014-2017 |
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| History Note: | 2018 |
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| DeCS ID: | 56950 | ||||||
| Unique ID: | D000073842 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2018/01/01 | ||||||
| Date of Entry: | 2017/07/11 | ||||||
| Revision Date: | 2018/05/23 |
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Trisomy 18 Syndrome
- Preferred
Trisomy E Syndrome
- Narrower
Complete Trisomy 18 Syndrome
- Narrower
Trisomy 18
- Narrower
Mosaic Trisomy 18 Syndrome
- Narrower
| Concept UI |
M000624074 |
| Scope note | A chromosome disorder associated with TRISOMY of all or part of CHROMOSOME 18. Clinical manifestations include INTRAUTERINE GROWTH RETARDATION; CLEFT PALATE; CONGENITAL HEART DEFECTS; MICROCEPHALY; MICROGNATHIA and clenched fists with overlapping fingers. Most affected fetuses do not survive to birth. Those who survive through their first year often have severe INTELLECTUAL DISABILITY. |
| Preferred term | Trisomy 18 Syndrome |
| Entry term(s) |
Trisomy 18 Syndromes |
| Concept UI |
M000642293 |
| Preferred term | Trisomy E Syndrome |
| Concept UI |
M000641927 |
| Preferred term | Complete Trisomy 18 Syndrome |
| Entry term(s) |
Edwards Syndrome |
| Concept UI |
M0583946 |
| Preferred term | Trisomy 18 |
| Concept UI |
M000624083 |
| Preferred term | Mosaic Trisomy 18 Syndrome |
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