Disease browser and phenotype portal

Hello! Guest! Please Login or Register! Clinician Mode

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: Brain Diseases (D001927)
Parent Node: Retrocochlear Diseases (D012181)
..Starting node ..Auditory Diseases, Central (D001304)
Child Nodes:
........Auditory Perceptual Disorders (D001308) 1
........Hearing Loss, Central (D006313) 16
Sister Nodes:
..Auditory Diseases, Central (D001304) 19
..Vestibulocochlear Nerve Diseases (D000160) 9
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	1058
Name:	Auditory Diseases, Central
Definition:	Disorders of hearing or auditory perception due to pathological processes of the AUDITORY PATHWAYS in the CENTRAL NERVOUS SYSTEM. These include CENTRAL HEARING LOSS and AUDITORY PERCEPTUAL DISORDERS.
Alternative IDs:
ParentIDs:	MESH:D001927\|MESH:D012181
TreeNumbers:	C09.218.807.186 \|C10.228.140.068
Synonyms:	Auditory Cortex Disorder \|Auditory Cortex Disorders \|Auditory Disease, Central \|Auditory Dysfunction, Central \|Auditory Pathway Disorders, Central \|Central Auditory Disease \|Central Auditory Diseases \|Central Auditory Dysfunction \|Central Auditory Pathway Disord
Slim Mappings:	Ear-nose-throat disease\|Nervous system disease
Reference:	MedGen: D001304 MeSH: D001304 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants