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Results 1 - 10 of 12 for Hearing "loss," autosomal dominant 78
  1. Keratitis-ichthyosis-deafness syndrome 
    ... recessive keratitis-ichthyosis-deafness syndrome Genetic Testing Registry: Autosomal dominant keratitis-ichthyosis-hearing loss syndrome Keratitis-ichthyosis-deafness syndrome, autosomal recessive KID ...
    https://medlineplus.gov/.../keratitis-ichthyosis-deafness-syndrome - Genetics
  2. Palmoplantar keratoderma with deafness 
    ... Prera E, Schild C, Aschendorff A, Arndt S. Autosomal dominant prelingual hearing loss with palmoplantar keratoderma syndrome: Variability in clinical expression ...
    https://medlineplus.gov/.../palmoplantar-keratoderma-with-deafness - Genetics
  3. MYH9-related disorder 
    ... no history of the disorder in their family. Autosomal dominant MYH9 ... MYH9-related disease National Organization for Rare Disorders ( ...
    https://medlineplus.gov/genetics/condition/myh9-related-disorder - Genetics
  4. Jackson-Weiss syndrome 
    ... feet. FGFR2 ... Agochukwu NB, Solomon BD, Muenke M. Hearing loss in syndromic craniosynostoses: otologic manifestations and clinical findings. ...
    https://medlineplus.gov/genetics/condition/jackson-weiss-syndrome - Genetics
  5. Bart-Pumphrey syndrome 
    ... impulses. GJB2 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ... Biochim Biophys Acta. 2013 Jan;1828(1):167-78. doi: 10.1016/j.bbamem.2012.06.024. Epub 2012 Jul 13. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/genetics/condition/bart-pumphrey-syndrome - Genetics
  6. Hystrix-like ichthyosis with deafness 
    ... not. GJB2 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ... Biochim Biophys Acta. 2013 Jan;1828(1):167-78. doi: 10.1016/j.bbamem.2012.06.024. Epub 2012 Jul 13. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/.../hystrix-like-ichthyosis-with-deafness - Genetics
  7. CHARGE syndrome 
    ... mutations in the CHD7 gene, it follows an autosomal dominant pattern of inheritance, which means one copy of ...
    https://medlineplus.gov/genetics/condition/charge-syndrome - Genetics
  8. Pfeiffer syndrome 
    ... FGFR1 FGFR2 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/genetics/condition/pfeiffer-syndrome - Genetics
  9. Williams syndrome 
    ... with Williams syndrome.Williams syndrome is considered an autosomal dominant condition because one copy of the altered chromosome ...
    https://medlineplus.gov/genetics/condition/williams-syndrome - Genetics
  10. Cleidocranial dysplasia 
    ... unknown. RUNX2 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/genetics/condition/cleidocranial-dysplasia - Genetics
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