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Results 1 - 10 of 336 for Disorder of ear
  1. Ménière disease 
    Ménière disease is a disorder of the inner ear that affects balance and hearing. This condition is characterized by sudden episodes of extreme dizziness (vertigo), a roaring sound in ...
    https://medlineplus.gov/genetics/condition/meniere-disease - Genetics
  2. Scalp-ear-nipple syndrome 
    ... Scalp-ear-nipple syndrome National Organization for Rare Disorders (NORD) SCALP-EAR-NIPPLE SYNDROME; SENS PubMed Marneros AG, Beck AE, ...
    https://medlineplus.gov/genetics/condition/scalp-ear-nipple-syndrome - Genetics
  3. Lacrimo-auriculo-dento-digital syndrome 
    ... auriculo-dento-digital (LADD) syndrome is a genetic disorder that mainly affects the eyes, ears, mouth, and hands. LADD syndrome is characterized by ... that make up the lacrimal glands, salivary glands, ears, skeleton, and many other organs.Mutations in the ... FGF10 gene in each cell is sufficient to cause the disorder.In some cases, an affected person inherits the ...
    https://medlineplus.gov/.../lacrimo-auriculo-dento-digital-syndrome - Genetics
  4. Townes-Brocks Syndrome 
    ... in each cell is sufficient to cause the disorder. Anal-ear-renal-radial malformation syndrome Deafness-imperforate anus-hypoplastic ... Imperforate anus-hand and foot anomalies syndrome Renal-ear-anal-radial syndrome (REAR) Sensorineural deafness-imperforate anus-hypoplastic ... for Rare Disorders (NORD) TOWNES-BROCKS SYNDROME 1; TBS1 TOWNES-BROCKS ...
    https://medlineplus.gov/genetics/condition/townes-brocks-syndrome - Genetics
  5. Smith-Magenis syndrome 
    ... and a hoarse voice. Some people with this disorder have ear abnormalities that lead to hearing loss. Affected individuals may have eye abnormalities that cause nearsightedness (myopia) and other vision problems. ... ...
    https://medlineplus.gov/genetics/condition/smith-magenis-syndrome - Genetics
  6. Congenital deafness with labyrinthine aplasia, microtia, and microdontia 
    ... aplasia, microtia, and microdontia National Organization for Rare Disorders (NORD) DEAFNESS, CONGENITAL, WITH INNER EAR AGENESIS, MICROTIA, AND MICRODONTIA PubMed Alsmadi O, Meyer ...
    https://medlineplus.gov/...rinthine-aplasia-microtia-and-microdontia - Genetics
  7. MN1 C-terminal truncation syndrome 
    ... occur in people with no history of the disorder in their family. CEBALID Craniofacial defects, dysmorphic ears, structural brain abnormalities, expressive language delay, and impaired ...
    https://medlineplus.gov/.../mn1-c-terminal-truncation-syndrome - Genetics
  8. GNAI3 gene 
    ... been found to cause auriculo-condylar syndrome, a disorder that primarily affects the development of the ears and lower jaw (mandible). The identified mutations change ...
    https://medlineplus.gov/genetics/gene/gnai3 - Genetics
  9. PLCB4 gene 
    ... been found to cause auriculo-condylar syndrome, a disorder that primarily affects the development of the ears and lower jaw (mandible). The identified mutations change ...
    https://medlineplus.gov/genetics/gene/plcb4 - Genetics
  10. HIVEP2-related intellectual disability 
    ... microcephaly). Less common health problems include seizures; recurrent ear infections; and eye disorders, such as eyes that do not look in ...
    https://medlineplus.gov/.../hivep2-related-intellectual-disability - Genetics
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