Phenotypes for disease #00261 (HDL2 (Huntington disease-like, type 2 (HDL2)), OMIM:606438)

16 entries on 1 page. Showing entries 1 - 16.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000001945 weight loss, dementia, psychiatric symptoms, dysarthria, chorea, rigidity, dystonia, action tremor, hyperreflexia, extensor plantars, primitive reflexes, bradykinesia, reduced movement, no dysmetria, not ambulatory, saccadic pursuit - - Familial, autosomal dominant - - - - - Johan den Dunnen 00003127
0000001946 weight loss, dementia, psychiatric symptoms, dysarthria, no chorea, rigidity, dystonia, action tremor, hyperreflexia, (extensor plantars), reduced movement, not ambulatory, no saccadic pursuit - - Familial, autosomal dominant 47y - 35y - - Johan den Dunnen 00003128
0000001947 weight loss, dementia, psychiatric symptoms, dysarthria, no chorea, rigidity, dystonia, no action tremor, hyperreflexia, extensor plantars, primitive reflexes, bradykinesia, reduced movement, not ambulatory, no saccadic pursuit - - Familial, autosomal dominant 52y - 35y - - Johan den Dunnen 00003129
0000331294 - - HDL2 Familial, autosomal dominant - - - - - Johan den Dunnen 00441911
0000331295 - - HDL2 Familial, autosomal dominant - - - - - Johan den Dunnen 00441912
0000331296 - - HDL2 Familial, autosomal dominant - - 45y - - Johan den Dunnen 00441913
0000331297 - - HDL2 Familial, autosomal dominant - - 41y - - Johan den Dunnen 00441914
0000331298 sudden onset cerebellar signs, uncontrolled diabetes, no clear family history - HDL2 Familial, autosomal dominant - - - - - Johan den Dunnen 00441915
0000331299 movement disorder - HDL2 Familial, autosomal dominant - - 42y - - Johan den Dunnen 00441916
0000331300 see paper; ..., 42y-mild choreic movements face and extremities; slight memory loss, bedside Mini-Mental Status score of 22/30; subcortical dementia - HDL2 Unknown 44y - - - - Johan den Dunnen 00441917
0000331301 56y-deceased; dementia, chorea - HDL2 Familial, autosomal dominant 56y - 34y - - Johan den Dunnen 00441918
0000331303 dementia, chorea, fragile X syndrome - HDL2 Familial, autosomal dominant 31y - 29y - - Johan den Dunnen 00441919
0000331304 dementia, parkinsonism - HDL2 Familial, autosomal dominant 38y - 28y - - Johan den Dunnen 00441920
0000331305 dementia, chorea, parkinsonism - HDL2 Familial, autosomal dominant 60y - 55y - - Johan den Dunnen 00441921
0000331306 depression, mild chorea, aggressiveness - HDL2 Familial, autosomal dominant 13y - 12y - - Johan den Dunnen 00441922
0000331307 depression, mild chorea - HDL2 Familial, autosomal dominant 41y - 39y - - Johan den Dunnen 00441923
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