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Results 1 - 4 of 4 for "Deafness," autosomal recessive 51
  1. Nonsyndromic hearing loss 
    ... RECESSIVE 28; DFNB28 DEAFNESS, AUTOSOMAL RECESSIVE 67; DFNB67 DEAFNESS, AUTOSOMAL RECESSIVE 36, WITH OR ... Xu P. The role of mitochondrial DNA mutations in hearing loss. Biochem Genet. 2013 Aug;51(7-8):588-602. doi: 10.1007/s10528- ...
    https://medlineplus.gov/genetics/condition/nonsyndromic-hearing-loss - Genetics
  2. Jervell and Lange-Nielsen syndrome 
    ... related heart abnormalities, but their hearing is normal. Autosomal recessive long QT syndrome (LQTS) Cardio-auditory-syncope syndrome Cardioauditory syndrome of Jervell and Lange-Nielsen Deafness, congenital, and functional heart disease Jervell-Lange Nielsen ...
    https://medlineplus.gov/.../jervell-and-lange-nielsen-syndrome - Genetics
  3. Alport syndrome 
    ... basement membrane nephropathy). ... Registry: Autosomal recessive Alport syndrome Genetic Testing Registry: X-linked Alport ...
    https://medlineplus.gov/genetics/condition/alport-syndrome - Genetics
  4. 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