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Results 1 - 10 of 15 for "Deafness," autosomal recessive 13
  1. Nonsyndromic hearing loss 
    ... DOMINANT 23; DFNA23 DEAFNESS, AUTOSOMAL RECESSIVE 21; DFNB21 DEAFNESS, AUTOSOMAL RECESSIVE 13; DFNB13 DEAFNESS, AUTOSOMAL RECESSIVE 17; DFNB17 DEAFNESS, AUTOSOMAL ...
    https://medlineplus.gov/genetics/condition/nonsyndromic-hearing-loss - Genetics
  2. Perrault syndrome 
    ... dysfunction, autosomal recessive inheritance Gonadal dysgenesis with sensorineural deafness, autosomal recessive inheritance Gonadal dysgenesis, XX type, with deafness Ovarian ...
    https://medlineplus.gov/genetics/condition/perrault-syndrome - Genetics
  3. 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
  4. Keratitis-ichthyosis-deafness syndrome 
    ... dominant keratitis-ichthyosis-hearing loss syndrome Keratitis-ichthyosis-deafness syndrome, autosomal recessive KID syndrome National Organization for Rare Disorders (NORD) ...
    https://medlineplus.gov/.../keratitis-ichthyosis-deafness-syndrome - Genetics
  5. Nearsightedness 
    ... DOMINANT; MYP2 MYOPIA 1, X-LINKED; MYP1 MYOPIA 13, X-LINKED; MYP13 MYOPIA 18, AUTOSOMAL RECESSIVE; MYP18 MYOPIA 3, AUTOSOMAL DOMINANT; MYP3 MYOPIA 6; ...
    https://medlineplus.gov/genetics/condition/nearsightedness - Genetics
  6. Charcot-Marie-Tooth disease 
    ... MOTOR AND SENSORY, WITH EXCESSIVE MYELIN FOLDING COMPLEX, AUTOSOMAL RECESSIVE NEUROPATHY, HEREDITARY MOTOR AND SENSORY, WITH DEAFNESS, IMPAIRED INTELLECTUAL DEVELOPMENT, AND ABSENT SENSORY LARGE MYELINATED ...
    https://medlineplus.gov/.../condition/charcot-marie-tooth-disease - Genetics
  7. Usher Syndrome From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Usher Syndrome/Learn More ... Usher Syndrome ... Find symptoms and other information about Usher syndrome. ... Genetic and Rare Diseases Information Center ... From the National ...
    https://rarediseases.info.nih.gov/diseases/7843/usher-syndrome - External Health Links
  8. Otospondylomegaepiphyseal dysplasia 
    ... and symptoms of the condition. Chondrodystrophy with ... National Organization for Rare Disorders (NORD) ...
    https://medlineplus.gov/.../otospondylomegaepiphyseal-dysplasia - Genetics
  9. GJB2 gene 
    ... Verselis VK. Aberrant Cx26 hemichannels and keratitis-ichthyosis-deafness syndrome: ... Autosomal Recessive Nonsyndromic Hearing Loss. 1998 Sep 28 [updated 2023 ...
    https://medlineplus.gov/genetics/gene/gjb2 - Genetics
  10. 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
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