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Results 1 - 8 of 8 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. 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
  5. 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
  6. 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
  7. 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
  8. Essential tremor 
    ... essential tremor appears to be inherited in an autosomal dominant pattern, which means one copy of an altered ...
    https://medlineplus.gov/genetics/condition/essential-tremor - Genetics