Disease Browser
|
Parent Node: Cri-du-Chat Syndrome (D003410) | Parent Node: Trisomy (D014314) | Parent Node: Uniparental Disomy (D024182) | ..Starting node ..Chromosome 5, uniparental disomy (C537762)
| Child Nodes:
|
Sister Nodes: | ..Chromosome 1, uniparental disomy 1q12 q21 (C538085)
| ..Chromosome 10, uniparental disomy of (C538292)
| ..Chromosome 15, trisomy mosaicism (C538037)
| ..Chromosome 16, uniparental disomy (C538043)
| ..Chromosome 21, uniparental disomy of (C536794)
| ..Chromosome 5, uniparental disomy (C537762)
| ..Chromosome 7, trisomy mosaic (C537822)
| ..Chromosome 8, mosaic trisomy (C537940)
| ..Chromosome 9, trisomy mosaic (C535454)
| ..Trisomy 22 mosaicism syndrome (C536796)
| ..Uniparental disomy of 11 (C536468)
| ..Uniparental disomy of 13 (C536469)
| ..Uniparental disomy of chromosome 2 (C536470)
| ..Uniparental disomy, paternal, chromosome 14 (C536471)
|
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
|
|
|
Term ID: | 2319 |
Name: | Chromosome 5, uniparental disomy |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D003410|MESH:D014314|MESH:D024182 |
TreeNumbers: | C10.597.606.643.180/C537762 |C16.131.077.262/C537762 |C16.131.260.190/C537762 |C16.320.180.190/C537762 |C23.550.210.050.750/C537762 |C23.550.210.182.500/C537762 |C23.550.210.645.890/C537762 |
Synonyms: | Mosaic trisomy of chromosome 5 |Uniparental disomy of 5 |
Slim Mappings: | Congenital abnormality|Genetic disease (inborn)|Nervous system disease|Pathology (process) |
Reference: |
MedGen: C537762
MeSH: C537762
OMIM:
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
|