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Results 1 - 10 of 12 for Autosomal dominant Parkinson disease 1
  1. Parkinson's disease 
    ... Parkinson disease PD Primary parkinsonism Genetic Testing Registry: Autosomal dominant Parkinson disease 1 Genetic Testing Registry: Autosomal dominant Parkinson disease 4 ...
    https://medlineplus.gov/genetics/condition/parkinsons-disease - Genetics
  2. LRRK2 gene 
    ... Network. A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease. Lancet. 2005 Jan 29-Feb 4;365(9457): ...
    https://medlineplus.gov/genetics/gene/lrrk2 - Genetics
  3. Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia 
    ... article on PubMed Central Kimonis VE, Watts GD. Autosomal dominant inclusion body myopathy, Paget disease of bone, and frontotemporal dementia. Alzheimer Dis Assoc Disord. 2005 Oct-Dec;19 Suppl 1:S44-7. doi: 10.1097/01.wad.0000183081. ...
    https://medlineplus.gov/...paget-disease-and-frontotemporal-dementia - Genetics
  4. Genetic Disorders From the National Institutes of Health (National Human Genome Research Institute)  
    Genetic Disorders/Start Here ... Genetic Disorders ... National Human Genome Research Institute ... From the National Institutes of Health ... A list of genetic, orphan and ...
    https://www.genome.gov/For-Patients-and-Families/Genetic-Disorders - External Health Links
  5. Restless legs syndrome 
    ... to have an autosomal dominant pattern of inheritance. Autosomal dominant inheritance suggests that one copy of an altered gene ... LEGS SYNDROME, SUSCEPTIBILITY TO, 1; RLS1 RESTLESS LEGS SYNDROME, SUSCEPTIBILITY TO, 2; RLS2 ...
    https://medlineplus.gov/genetics/condition/restless-legs-syndrome - Genetics
  6. Huntington Disease From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Huntington's Disease/Learn More ... Huntington's Disease ... Genetic and Rare Diseases Information Center ... From the National Institutes of Health ... Find symptoms and ...
    https://rarediseases.info.nih.gov/diseases/6677/huntington-disease - External Health Links
  7. Spinocerebellar Ataxias Including Machado-Joseph Disease From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Cerebellar Disorders/Specifics ... Cerebellar Disorders ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Spinocerebellar ...
    https://www.ninds.nih.gov/...taxias-including-machado-joseph-disease - External Health Links
  8. Intestinal pseudo-obstruction 
    ... Pseudoobstructive syndrome Genetic Testing Registry: Visceral neuropathy, familial, 1, autosomal recessive Genetic Testing Registry: Visceral neuropathy, familial, 3, autosomal dominant Genetic Testing Registry: Intestinal pseudoobstruction, neuronal, chronic idiopathic, ...
    https://medlineplus.gov/.../condition/intestinal-pseudo-obstruction - Genetics
  9. Wolff-Parkinson-White syndrome 
    ... 300. Citation on PubMed Light PE. Familial Wolff-Parkinson-White Syndrome: a disease of glycogen storage or ion channel dysfunction? J Cardiovasc Electrophysiol. 2006 May;17 Suppl 1:S158-S161. doi: 10.1111/j.1540-8167. ...
    https://medlineplus.gov/.../condition/wolff-parkinson-white-syndrome - Genetics
  10. Congenital mirror movement disorder 
    ... life in people with neurodegenerative disorders such as Parkinson's disease. Mirror ... prevalence is thought to be less than 1 in 1 million. Researchers suggest that some mildly ...
    https://medlineplus.gov/.../congenital-mirror-movement-disorder - Genetics
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