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Searched for "Hearing Problems in Children".

1. Alström syndrome condition summary
   Found in link title: Hearing Problems in Children

   Related genes:

   • ALMS1
2. CHARGE syndrome condition summary
   Found in link title: Hearing Problems in Children

   Related genes:

   • CHD7
3. congenital deafness with labyrinthine aplasia, microtia, and microdontia condition summary
   Found in link title: Hearing Problems in Children

   Related genes:

   • FGF3
4. nonsyndromic deafness condition summary
   Found in link title: Hearing Problems in Children

   Related genes and chromosomes:

   • mitochondrial DNA
   • ACTG1
   • ATP2B2
   • CDH23
   • CLDN14
   • COCH
   • COL11A2
   • DFNA5
   • DFNB31
   • DFNB59
   • ESPN
   • EYA4
   • GJB2
   • GJB3
   • GJB6
   • KCNQ4
   • LHFPL5
   • MT-RNR1
   • MT-TS1
   • MYO15A
   • MYO1A
   • MYO6
   • MYO7A
   • OTOF
   • PCDH15
   • POU3F4
   • SLC26A4
   • STRC
   • TECTA
   • TMC1
   • TMIE
   • TMPRSS3
   • TRIOBP
   • USH1C
   • WFS1
5. thiamine-responsive megaloblastic anemia syndrome condition summary
   Found in link title: Hearing Problems in Children

   Related genes:

   • SLC19A2
6. Usher syndrome condition summary
   Found in link title: Hearing Problems in Children

   Related genes:

   • CDH23
   • CLRN1
   • GPR98
   • MYO7A
   • PCDH15
   • USH1C
   • USH1G
   • USH2A