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Phenotypes for disease #01451 (DYT11 (dystonia, myoclonic, type 11 (DYT11)), OMIM:159900)
Legend
Please note that a short description of a certain column can be displayed when you move your mouse cursor over the column's header and hold it still. Below, a more detailed description is shown per column.
Phenotype details
: additional information on the phenotype of the individual, preferably use HPO terms only (http://www.human-phenotype-ontology.org/)
Diagnosis/Initial
: initial diagnosis, before molecular testing
Diagnosis/Definite
: phenotype individual after molecular testing (OMIM abbreviation)
Inheritance
: Indicates the inheritance of the phenotype in the family; unknown, familial (autosomal/X-linked, dominant/ recessive), paternal (Y-linked), maternal (mitochondrial), isolated (sporadic) or complex
All options:
Unknown
Familial
Familial, autosomal dominant
Familial, autosomal recessive
Familial, X-linked
Familial, X-linked dominant
Familial, X-linked dominant, male sparing
Familial, X-linked recessive
Paternal, Y-linked
Maternal, mitochondrial
Isolated (sporadic)
Di-genic
Complex
- = Not applicable
Age/Examination
: age at which the individual was examined.
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Age/Diagnosis
: age diagnosis was confirmed
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Age/Onset
: Age first symptoms disease appeared in individual:
35y = 35 years
04y08m = 4 years and 8 months
00y00m01d12h = 1 day and 12 hours
18y? = around 18 years
30y-40y = between 30 and 40 years
>54y = older than 54
? = unknown
Phenotype/Onset
: individual's phenotype at Age/Onset described using HPO
Protein
: result from protein staining
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18 entries on 1 page. Showing entries 1 - 18.
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How to query
Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000025672
see paper; cervical/axial dystonia at rest, writer’s cramp, action-induced foot dystonia with walking, myoclonic jerks legs/arms, increasing with action, positive effect of alcohol on jerks, complaints of hyperventilation or panic attacks; high-frequency continuous myoclonus legs while standing, causing unsteadiness; 3/5 cases cardiac arrhythmias, attacks of painful cramps upper/lower limbs
-
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00029649
0000051930
psychiatric symptoms (HP:0000708), anxiety (HP:0000739), phobia (HP:?), jerking movement (HP:0007087), exaggerated startle response (HP:0002267)
-
-
Familial, autosomal dominant
-
-
05y
-
-
Jamie Zeegers
00072225
0000051931
upper limb muscle jerking (HP:0007087), dystonic posture (HP:0001332), laterocollis (HP:0000473)
-
-
Familial, autosomal dominant
-
-
-
-
-
Jamie Zeegers
00072226
0000051935
upper limb and neck myoclonus (HP:0001336), no dystonia (HP:0001332), no seizures in childhood (-HP:0001250), generalized spike-wave activity (HP:0001326)
-
-
Familial, autosomal dominant
-
-
-
-
-
Jamie Zeegers
00072230
0000051936
upper limb myoclonus (HP:0001336), no dystonia (-HP:0001332), generalized tonic–clonic seizures (HP:0002069), generalized polyspike wave activity (HP:?)
-
-
Familial, autosomal dominant
-
-
-
-
-
Jamie Zeegers
00072231
0000051937
upper limb myoclonus (HP:0001336), no dystonia (-HP:0001332), febrile seizures (HP:0002373)
-
-
Familial, autosomal dominant
-
-
-
-
-
Jamie Zeegers
00072232
0000051938
upper limb and neck myoclonus (HP:0001336), no dystonia (-HP:0001332), no seizures in childhood (-HP:0001250), generalized tonic–clonic seizures (HP:0002069)
-
-
Familial, autosomal dominant
-
-
-
-
-
Jamie Zeegers
00072233
0000051939
upper limb, trunk and neck myoclonus (HP:0001336), cervical dystonia (HP:0000473), vocal dystonia (HP:?), no epilepsy (-HP:0001250), myoclonic jerks (HP:0001336)
-
-
Familial, autosomal dominant
-
-
-
-
-
Jamie Zeegers
00072234
0000051940
upper limb myoclonus (HP:0001336), vocal dystonia (HP:?), no epilepsy (-HP:0001250)
-
-
Familial, autosomal dominant
-
-
-
-
-
Jamie Zeegers
00072236
0000051947
dependent of a walker (HP:?), diarrhoeas (HP:?), inability to control defecation (HP:?), myoclonic jerks (HP:0001336),
-
-
Familial, autosomal dominant
-
-
00y09m
Myoclonic jerks (HP:0001336)
-
Jamie Zeegers
00072242
0000051948
writer’s cramp (HP:0002356), that alcohol rather induced dystonia (HP:?)
-
-
Familial, autosomal dominant
-
-
-
-
-
Jamie Zeegers
00072243
0000051949
hemidystonia (HP:?), myoclonal jerks (HP:0001336), interfered severely with balance (HP:0002141) and walking (HP:0002355), psychiatric disorder (HP:0000708), reduced myoclonus after alcohol intake (HP:?)
-
-
Familial, autosomal dominant
-
-
-
-
-
Jamie Zeegers
00072244
0000078602
see paper; ..., delay in motor development (HP:0001270), dystonia (HP:0001332), myoclonus (HP:0001336)
-
-
Familial, autosomal dominant
06y
-
02y08m
-
-
Johan den Dunnen
00072203
0000078603
see paper; ..., MDS, bilateral carotid artery stenosis mimicking Moya–Moya disease
-
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00100411
0000079164
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00100943
0000242119
(+) Dystonia,(+) Myoclonus
2y
-
Unknown
-
-
-
-
-
Andreas Laner
00320074
0000337701
HP:0001332 Dystonia, HP:0002333 Motor deterioration, HP:0001336 Myoclonus, HP:0001337 Tremor.
56
Dystonia-11, myoclonic (AD, #159900)
Familial, autosomal dominant
32
56y
21y
-
-
Maria Elena García Paya
00448525
0000351355
-
DYT11
DYT11
Familial, autosomal dominant
-
-
-
-
-
Marketa Wayhelova
00465957
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