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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)
Parent Node: Sex Chromosome Disorders of Sex Development (D058533)
..Starting node ..Male sterility due to Y-chromosome deletions (C536297)
Child Nodes:
Sister Nodes:
..Freemartinism (D005611)
..Gonadal Dysgenesis, Mixed (D006060)
..Klinefelter Syndrome (D007713)
..Male sterility due to Y-chromosome deletions (C536297)
..Triple X syndrome (C535318)
..Turner Syndrome (D014424) 2
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	6726
Name:	Male sterility due to Y-chromosome deletions
Definition:
Alternative IDs:
ParentIDs:	MESH:D002872\|MESH:D012729\|MESH:D058533
TreeNumbers:	C12.706.316.795/C536297 \|C13.351.875.253.795/C536297 \|C16.131.260.830.835/C536297 \|C16.131.939.316.795/C536297 \|C16.320.180.830.835/C536297 \|C19.391.119.795/C536297 \|C23.550.210.050.500.500/C536297 \|C23.550.210.815/C536297
Synonyms:	Partial deletion of chromosome Y \|Partial deletion of the long arm of the Y chromosome \|Partial deletion of Y \|Partial deletion of Y chromosome short arm \|Y chromosome deletions \|Y chromosome microdeletions \|Y-chromosome microdeletions
Slim Mappings:	Congenital abnormality\|Endocrine system disease\|Genetic disease (inborn)\|Pathology (process)\|Urogenital disease (female)\|Urogenital disease (male)
Reference:	MedGen: C536297 MeSH: C536297 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants