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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: Chromosome Deletion (D002872)
Parent Node: Sex Chromosome Aberrations (D012729)
..Starting node ..X chromosome, monosomy Xq28 (C536755)
Child Nodes:
Sister Nodes:
..49,XXXXX syndrome (C535319)
..Chromosome Xq duplication syndrome (C536732)
..Male sterility due to Y-chromosome deletions (C536297)
..Tetrasomy X (C536502)
..Triple X syndrome (C535318)
..X chromosome, duplication Xq13 1 q21 1 (C536753)
..X chromosome, monosomy Xp22 pter (C536754)
..X chromosome, monosomy Xq28 (C536755)
..X chromosome, trisomy Xp3 (C536756)
..X chromosome, trisomy Xpter Xq13 (C536731)
..X chromosome, trisomy Xq25 (C536733)
..XYY Karyotype (D014997) 1
..Young Hughes syndrome (C536715)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	11813
Name:	X chromosome, monosomy Xq28
Definition:
Alternative IDs:
ParentIDs:	MESH:D002872\|MESH:D012729
TreeNumbers:	C23.550.210.050.500.500/C536755 \|C23.550.210.815/C536755
Synonyms:	Deletion Xq28 \|Monosomy Xq28
Slim Mappings:	Pathology (process)
Reference:	MedGen: C536755 MeSH: C536755 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants