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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: Presbycusis (D011304)
..Starting node ..Presbycusis 2 (C567834)
Child Nodes:
Sister Nodes:
..Age-Related Hearing Impairment 1 (C567305)
..Presbycusis 2 (C567834)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	9261
Name:	Presbycusis 2
Definition:
Alternative IDs:	OMIM:612976
ParentIDs:	MESH:D011304
TreeNumbers:	C09.218.458.341.887.772/C567834 \|C10.597.751.418.341.887.772/C567834 \|C23.888.592.763.393.341.887.772/C567834
Synonyms:	Age-Related Hearing Impairment 2 \|ARHI2 \|PRESBYCUSIS 2
Slim Mappings:	Ear-nose-throat disease\|Nervous system disease\|Signs and symptoms
Reference:	MedGen: C567834 MeSH: C567834 OMIM: 612976; Genes:
Phenotypes
Disease Causing ClinVar Variants