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Results 1 - 10 of 52 for Cerebellar disorder
  1. VLDLR-associated cerebellar hypoplasia 
    ... Autosomal recessive cerebellar hypoplasia with cerebral gyral simplification Cerebellar disorder, nonprogressive, with mental retardation Cerebellar hypoplasia and mental ...
    https://medlineplus.gov/.../vldlr-associated-cerebellar-hypoplasia - Genetics
  2. Autosomal dominant cerebellar ataxia, deafness, and narcolepsy 
    ... dominant cerebellar ataxia, deafness and narcolepsy Autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome National Organization for Rare Disorders (NORD) ClinicalTrials.gov CEREBELLAR ATAXIA, DEAFNESS, AND NARCOLEPSY, ...
    https://medlineplus.gov/...cerebellar-ataxia-deafness-and-narcolepsy - Genetics
  3. DNMT1 gene 
    ... with a nervous system disorder called autosomal dominant cerebellar ataxia, deafness, and narcolepsy (ADCADN). Features of this disorder include difficulty coordinating movements (ataxia), hearing loss caused ...
    https://medlineplus.gov/genetics/gene/dnmt1 - Genetics
  4. Gillespie syndrome 
    ... ataxia-oligophrenia Genetic Testing Registry: Gillespie syndrome Aniridia-cerebellar ataxia-intellectual disability syndrome National Organization for Rare Disorders (NORD) GILLESPIE SYNDROME; GLSP PubMed Dentici ML, Barresi ...
    https://medlineplus.gov/genetics/condition/gillespie-syndrome - Genetics
  5. CASK-related intellectual disability 
    ... Disorders (NORD) FG SYNDROME 4; FGS4 INTELLECTUAL DEVELOPMENTAL DISORDER WITH MICROCEPHALY AND PONTINE AND CEREBELLAR HYPOPLASIA; MICPCH PubMed Burglen L, Chantot-Bastaraud S, ...
    https://medlineplus.gov/.../cask-related-intellectual-disability - Genetics
  6. Gordon Holmes syndrome 
    ... ataxia Genetic Testing Registry: Cerebellar ataxia-hypogonadism syndrome Cerebellar ataxia-hypogonadism syndrome National Organization for Rare Disorders (NORD) ClinicalTrials.gov GORDON HOLMES SYNDROME; GDHS PubMed ...
    https://medlineplus.gov/genetics/condition/gordon-holmes-syndrome - Genetics
  7. Pol III-related leukodystrophy 
    ... TACH); leukodystrophy with oligodontia (LO); or hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum (HCAHC). Because these disorders were later found to have the same genetic ...
    https://medlineplus.gov/.../condition/pol-iii-related-leukodystrophy - Genetics
  8. Combined pituitary hormone deficiency 
    ... hormone deficiency, combined 1 Short stature-pituitary and cerebellar defects-small sella turcica syndrome National Organization for Rare Disorders (NORD) ClinicalTrials.gov PITUITARY HORMONE DEFICIENCY, COMBINED, 3; ...
    https://medlineplus.gov/.../combined-pituitary-hormone-deficiency - Genetics
  9. POLR3B gene 
    ... TACH); leukodystrophy with oligodontia (LO); or hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum (HCAHC). Because these disorders were later found to have the same genetic ...
    https://medlineplus.gov/genetics/gene/polr3b - Genetics
  10. POLR3A gene 
    ... TACH); leukodystrophy with oligodontia (LO); or hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum (HCAHC). Because these disorders were later found to have the same genetic ...
    https://medlineplus.gov/genetics/gene/polr3a - Genetics
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