Retinal and hearing impairment genetic mutation database
LOVD v.2.0 Build 37 [
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Please select a gene database:
CDH23 (cadherin-related 23)
CEACAM16 (carcinoembryonic antigen-related cell adhesion molecule 16)
CERKL (ceramide kinase-like)
CHM (choroideremia (Rab escort protein 1))
CLDN14 (claudin 14)
CLRN1 (clarin 1)
GPR98 (G protein-coupled receptor 98)
MYO15A (myosin XVA)
MYO6 (myosin VI)
MYO7A (myosin VIIA)
OTOF (otoferlin)
PCDH15 (protocadherin-related 15)
PDZD7 (PDZ domain containing 7)
SLC26A4 (solute carrier family 26 (anion exchanger), member 4)
TECTA (tectorin alpha)
TMC1 (transmembrane channel-like 1)
USH1C (Usher syndrome 1C)
USH1G (Usher syndrome 1G)
USH2A (Usher syndrome 2A)
WHRN (Whirlin)
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LOVD v.2.0
Build 37
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Leiden University Medical Center