Disease Browser
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Parent Node: Abnormalities, Multiple (D000015) | Parent Node: Chromosome Disorders (D025063) | Parent Node: Trisomy (D014314) | ..Starting node ..Trisomy 18-Like Syndrome (C563382)
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Sister Nodes: | ..6q+ Syndrome, Partial (C537810)
| ..Chromosome 1, duplication 1p21 p32 (C535364)
| ..Chromosome 1, q42 11 q42 12 duplication (C538082)
| ..Chromosome 1, trisomy 1q32 qter (C538083)
| ..Chromosome 1, trisomy 1q42 qter (C538084)
| ..Chromosome 1, uniparental disomy 1q12 q21 (C538085)
| ..Chromosome 10, trisomy 10p (C538290)
| ..Chromosome 10, trisomy 10pter p13 (C538291)
| ..Chromosome 10, uniparental disomy of (C538292)
| ..Chromosome 10q duplication syndrome (C537804)
| ..Chromosome 11, partial trisomy 11q (C538294)
| ..Chromosome 11q trisomy (C538297)
| ..Chromosome 12, 12p trisomy (C538299)
| ..Chromosome 12, trisomy 12q (C538300)
| ..Chromosome 13p duplication (C535450)
| ..Chromosome 13q trisomy (C535485)
| ..Chromosome 14 trisomy (C535488)
| ..Chromosome 14, trisomy mosaic (C535489)
| ..Chromosome 14q, proximal duplication (C538032)
| ..Chromosome 14q, terminal duplication (C538034)
| ..Chromosome 15, trisomy mosaicism (C538037)
| ..Chromosome 15q, trisomy (C538040)
| ..Chromosome 16, trisomy (C538041)
| ..Chromosome 16, trisomy 16q (C538042)
| ..Chromosome 17 trisomy (C538044)
| ..Chromosome 17, trisomy 17p (C538048)
| ..Chromosome 17, trisomy 17p11 2 (C536578)
| ..Chromosome 17, trisomy 17q22 (C536579)
| ..Chromosome 18, trisomy 18p (C538307)
| ..Chromosome 18, trisomy 18q (C538308)
| ..Chromosome 19, trisomy 19q (C538311)
| ..Chromosome 1q, duplication 1q12 q21 (C538312)
| ..Chromosome 2, trisomy 2p (C538318)
| ..Chromosome 2, trisomy 2p13 p21 (C535365)
| ..Chromosome 2, trisomy 2pter p24 (C535366)
| ..Chromosome 2, trisomy 2q (C535367)
| ..Chromosome 2, trisomy 2q37 (C535368)
| ..Chromosome 20, trisomy (C535372)
| ..Chromosome 21, uniparental disomy of (C536794)
| ..Chromosome 22, trisomy (C536799)
| ..Chromosome 22, trisomy q11 q13 (C536800)
| ..Chromosome 3 duplication syndrome (C536803)
| ..Chromosome 3, trisomy 3p (C536811)
| ..Chromosome 3, trisomy 3p25 (C536812)
| ..Chromosome 3, trisomy 3q (C536813)
| ..Chromosome 3, trisomy 3q13 2 q25 (C537634)
| ..Chromosome 4, partial trisomy distal 4q (C537642)
| ..Chromosome 4, trisomy 4q (C537644)
| ..Chromosome 4, trisomy 4q21 (C537645)
| ..Chromosome 4, trisomy 4q25 qter (C537646)
| ..Chromosome 5, monosomy 5q35 (C537647)
| ..Chromosome 5, trisomy 5pter p13 3 (C537649)
| ..Chromosome 5, trisomy 5q (C537650)
| ..Chromosome 5, uniparental disomy (C537762)
| ..Chromosome 6, trisomy 6p (C537811)
| ..Chromosome 6, trisomy 6q (C537812)
| ..Chromosome 7, trisomy 7p (C537819)
| ..Chromosome 7, trisomy 7p13 p12 2 (C537820)
| ..Chromosome 7, trisomy 7q (C537821)
| ..Chromosome 7, trisomy mosaic (C537822)
| ..Chromosome 8, mosaic trisomy (C537940)
| ..Chromosome 8, partial trisomy (C537941)
| ..Chromosome 8, trisomy (C537942)
| ..Chromosome 8, trisomy 8p (C538019)
| ..Chromosome 8, trisomy 8q (C538020)
| ..Chromosome 9, partial trisomy 9p (C538026)
| ..Chromosome 9, trisomy (C538028)
| ..Chromosome 9, trisomy 9p (C538029)
| ..Chromosome 9, trisomy 9q (C538030)
| ..Chromosome 9, trisomy 9q32 (C535453)
| ..Chromosome 9, trisomy mosaic (C535454)
| ..Chromosome Xq duplication syndrome (C536732)
| ..Distal Trisomy 10q Syndrome (C538087)
| ..Duplication 4p Syndrome (C537643)
| ..Partial Duplication 15q Syndrome (C538036)
| ..Partial Trisomy 3q Syndrome (C537635)
| ..Patau syndrome (C536305)
| ..Pseudotrisomy 13 syndrome (C535829)
| ..Triple X syndrome (C535318)
| ..Trisomy 18 (C580500)
| ..Trisomy 18-Like Syndrome (C563382)
| ..Trisomy 20p (C535371)
| ..Trisomy 22 mosaicism syndrome (C536796)
| ..Warburton Anyane Yeboa syndrome (C536682)
| ..X chromosome, duplication Xq13 1 q21 1 (C536753)
| ..X chromosome, trisomy Xp3 (C536756)
| ..X chromosome, trisomy Xpter Xq13 (C536731)
| ..X chromosome, trisomy Xq25 (C536733)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 11283 |
Name: | Trisomy 18-Like Syndrome |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D000015|MESH:D014314|MESH:D025063 |
TreeNumbers: | C16.131.077/C563382 |C16.131.260/C563382 |C16.320.180/C563382 |C23.550.210.050.750/C563382 |C23.550.210.182.500/C563382 |
Synonyms: | |
Slim Mappings: | Congenital abnormality|Genetic disease (inborn)|Pathology (process) |
Reference: |
MedGen: C563382
MeSH: C563382
OMIM: 601161;
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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