Hearing Loss Disease Portal


 
Switch to table view
Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandHearing Loss, Sensorineural (D006319)
Parent Node:
expandTooth Discoloration (D014075)
..Starting node
..expandSensorineural Hearing Loss, Retinal Pigment Epithelium Lesions, Discolored Teeth (C566560)

       Child Nodes:



 Sister Nodes: 
..expandSensorineural Hearing Loss, Retinal Pigment Epithelium Lesions, Discolored Teeth (C566560)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:10127
Name:Sensorineural Hearing Loss, Retinal Pigment Epithelium Lesions, Discolored Teeth
Definition:
Alternative IDs:
ParentIDs:MESH:D006319|MESH:D014075
TreeNumbers:C07.793.735/C566560 |C09.218.458.341.887/C566560 |C10.597.751.418.341.887/C566560 |C23.888.592.763.393.341.887/C566560
Synonyms:
Slim Mappings:Ear-nose-throat disease|Mouth disease|Nervous system disease|Signs and symptoms
Reference: MedGen: C566560
MeSH: C566560
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants