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Results 1 - 9 of 9 for Hearing "loss," autosomal dominant 76
  1. 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
  2. Fanconi anemia 
    ... Very rarely, Fanconi anemia is inherited in an autosomal dominant pattern or in an X-linked pattern. An autosomal dominant pattern of inheritance means one copy of the ...
    https://medlineplus.gov/genetics/condition/fanconi-anemia - Genetics
  3. 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
  4. Spondyloepiphyseal dysplasia with metatarsal shortening 
    ... properly. COL2A1 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/...seal-dysplasia-with-metatarsal-shortening - Genetics
  5. 10q26 deletion syndrome 
    ... chromosome 10 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/genetics/condition/10q26-deletion-syndrome - Genetics
  6. Saethre-Chotzen syndrome 
    ... chromosome 7 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/genetics/condition/saethre-chotzen-syndrome - Genetics
  7. Campomelic dysplasia 
    ... dysplasia. SOX9 Campomelic dysplasia is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/genetics/condition/campomelic-dysplasia - Genetics
  8. Apert syndrome 
    ... feet. FGFR2 Apert syndrome is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/genetics/condition/apert-syndrome - Genetics
  9. Cerebral cavernous malformation 
    ... unknown. CCM2 KRIT1 PDCD10 This condition has an autosomal dominant pattern of inheritance, which means one copy of ...
    https://medlineplus.gov/.../cerebral-cavernous-malformation - Genetics