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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Trisomy (D014314)
Parent Node: Uniparental Disomy (D024182)
..Starting node ..Chromosome 10, uniparental disomy of (C538292)
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:	2186
Name:	Chromosome 10, uniparental disomy of
Definition:
Alternative IDs:
ParentIDs:	MESH:D014314\|MESH:D024182
TreeNumbers:	C23.550.210.050.750/C538292 \|C23.550.210.182.500/C538292 \|C23.550.210.645.890/C538292
Synonyms:	Mosaic trisomy 10 \|Uniparental disomy of 10
Slim Mappings:	Pathology (process)
Reference:	MedGen: C538292 MeSH: C538292 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants