58 genes and genomic entities tagged
“deafness”
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58 genes and genomic entities
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- ADGRV1
- CABP2
- CDC14A
- CDH23
- CIB2
- CLDN14
- COCH
- COL11A2
- DFNB59
- EDN3
- EDNRB
- EPS8
- ESPN
- ESRRB
- FGF3
- FOXE1
- GATA2
- GATA3
- GIPC3
- GJB2
- GREB1L
- GRXCR1
- HGF
- ILDR1
- KCNQ1
- LHFPL5
- LOXHD1
- LRTOMT
- MARVELD2
- MITF
- MYO15A
- MYO3A
- MYO6
- MYO7A
- OTOA
- OTOF
- OTOG
- OTOGL
- PAX3
- PCDH15
- PDZD7
- POU3F4
- PTPRQ
- RDX
- S1PR2
- SLC26A4
- SLITRK6
- STRC
- TECTA
- TMC1
- TMIE
- TMPRSS3
- TPRN
- TRIOBP
- USH1C
- USH1G
- USH2A
- WHRN
Tagged
- 5'UTR
- acadm
- adult-onset
- adult onset neurodegenerative
- cancer
- cardiac
- clinical trial
- cnv
- deafness
- deep intronic
- dermatological
- digenic
- disputed
- endocrine
- for reivew
- for review
- founder
- gastrointestinal
- GI
- haematological
- immunological
- liver
- Medicare
- metabolic
- mtDNA
- neurological
- new gene name
- ophthalmological
- paediatric-onset
- pharmacogenomic
- refuted
- renal
- respiratory
- review
- skeletal
- som
- somatic
- STR
- SV/CNV
- technically challenging
- treatable
- treatment
- umccr
- UTR
- vascular