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Results 1 - 10 of 20 for Hearing "loss," autosomal dominant 90
  1. Nonsyndromic hearing loss 
    ... sufficient to cause the condition. Most people with autosomal dominant hearing loss inherit an altered copy of the gene from ... mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss. Hum Mutat. 2011 Jul;32(7):825-34. ...
    https://medlineplus.gov/genetics/condition/nonsyndromic-hearing-loss - Genetics
  2. Branchiootorenal/branchiootic syndrome 
    ... SIX5 BOR/BO syndrome is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder. In about 90 percent of cases, an affected person inherits the ...
    https://medlineplus.gov/.../branchiootorenal-branchiootic-syndrome - Genetics
  3. 22q11.2 deletion syndrome 
    ... the 22q11.2 deletion were diagnosed with the autosomal dominant form of Opitz G/BBB syndrome and Cayler ... inheritance of 22q11.2 deletion syndrome is considered autosomal dominant because a deletion in one copy of chromosome ...
    https://medlineplus.gov/genetics/condition/22q112-deletion-syndrome - Genetics
  4. Charcot-Marie-Tooth disease 
    ... and most intermediate forms are inherited in an autosomal dominant pattern. This pattern of inheritance means that one ... mild symptoms of the disorder.Some cases of autosomal dominant or type X Charcot-Marie-Tooth disease result ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics
  5. Cornelia de Lange syndrome 
    ... gene, the condition is considered to have an autosomal dominant pattern of inheritance. Autosomal dominant inheritance means one copy of the altered gene ...
    https://medlineplus.gov/.../condition/cornelia-de-lange-syndrome - Genetics
  6. Sotos syndrome 
    ... helped researchers determine that Sotos syndrome has an autosomal dominant pattern of inheritance. Autosomal dominant inheritance means one copy of the altered gene ...
    https://medlineplus.gov/genetics/condition/sotos-syndrome - Genetics
  7. Osteogenesis imperfecta 
    ... COL1A1 or COL1A2 gene, osteogenesis imperfecta has an autosomal dominant pattern of inheritance, which means one copy of ... gene. Type V is also inherited in an autosomal dominant pattern.Less commonly, osteogenesis imperfecta has an autosomal ...
    https://medlineplus.gov/genetics/condition/osteogenesis-imperfecta - Genetics
  8. Nager syndrome 
    ... in the SF3B4 gene, Nager syndrome follows an autosomal dominant inheritance pattern, which means one copy of the ... person inherits the mutation from one affected parent. Autosomal dominant Nager syndrome may also be caused by mutations ...
    https://medlineplus.gov/genetics/condition/nager-syndrome - Genetics
  9. Treacher Collins syndrome 
    ... TCOF1 or POLR1D gene, it is considered an autosomal dominant condition, which means one copy of the altered ... the disorder in their family. In the remaining autosomal dominant cases, a person with Treacher Collins syndrome inherits ...
    https://medlineplus.gov/genetics/condition/treacher-collins-syndrome - Genetics
  10. Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome 
    ... syndrome. TP63 This condition is inherited in an autosomal dominant pattern, which means one copy of the altered ...
    https://medlineplus.gov/...odermal-defects-cleft-lip-palate-syndrome - Genetics
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