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Results 1 - 8 of 8 for "Deafness," autosomal recessive 44
  1. STRC gene 
    ... in affected males. More About This Health Condition deafness, autosomal recessive 16 DFNB16 STRC_HUMAN Tests of STRC PubMed ...
    https://medlineplus.gov/genetics/gene/strc - Genetics
  2. DOORS syndrome 
    ... not show signs and symptoms of the condition. Autosomal recessive deafness-onychodystrophy syndrome Deafness, onychodystrophy, osteodystrophy, and mental retardation ...
    https://medlineplus.gov/genetics/condition/doors-syndrome - Genetics
  3. Sensorineural deafness and male infertility 
    ... and male infertility. CATSPER2 STRC chromosome 15 Sensorineural deafness and male infertility is inherited in an autosomal recessive pattern, which means both copies of chromosome 15 ...
    https://medlineplus.gov/...nsorineural-deafness-and-male-infertility - Genetics
  4. Burn-McKeown syndrome 
    ... siblings. Clin Dysmorphol. 1992 Jul;1(3):137-44. Citation on PubMed Hing AV, Leblond C, Sze RW, Starr JR, Monks S, Parisi MA. A novel oculo-oto-facial dysplasia in a Native Alaskan community with autosomal recessive inheritance. Am J Med Genet A. 2006 Apr ...
    https://medlineplus.gov/genetics/condition/burn-mckeown-syndrome - Genetics
  5. Congenital deafness with labyrinthine aplasia, microtia, and microdontia 
    ... mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated gene, but they typically do not show signs and symptoms of the condition. Congenital deafness with inner ear agenesis, microtia, and microdontia Deafness ...
    https://medlineplus.gov/...rinthine-aplasia-microtia-and-microdontia - Genetics
  6. MEGDEL syndrome 
    ... mutations. The parents of an individual with an autosomal recessive condition each carry one ... sensorineural deafness, encephalopathy, and Leigh-like syndrome 3-methylglutaconic aciduria ...
    https://medlineplus.gov/genetics/condition/megdel-syndrome - Genetics
  7. Riboflavin transporter deficiency neuronopathy 
    ... mutations. The parents of an individual with an autosomal recessive condition each carry ... with deafness Progressive bulbar palsy with sensorineural deafness Riboflavin transporter ...
    https://medlineplus.gov/...lavin-transporter-deficiency-neuronopathy - Genetics
  8. 6q24-related transient neonatal diabetes mellitus 
    ... ZFP57 gene mutations, it is inherited in an autosomal recessive pattern. Autosomal recessive inheritance means both copies of the gene in ... mutations. The parents of an individual with an autosomal recessive condition each carry one copy of the mutated ...
    https://medlineplus.gov/...ated-transient-neonatal-diabetes-mellitus - Genetics