Global Variome shared LOVD
C14orf132 (chromosome 14 open reading frame 132)
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Phenotypes for disease #05355 (spastic ataxia (ataxia, spastic))
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.
Diagnosis/Initial
: initial diagnosis, before molecular testing
Diagnosis/Definite
: phenotype individual after molecular testing (OMIM abbreviation)
Phenotype details
: additional information on the phenotype of the individual, preferably use HPO terms only (http://www.human-phenotype-ontology.org/)
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/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
How to query this table
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all entries beginning with 'p.(Arg'
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Date
2020
all entries matching the year 2020
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Date
2020-03|2020-04
all entries matching March or April, 2020
!
Date
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all entries not matching March, 2020
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Date
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all entries before the year 2020
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Date
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Date
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all entries after June, 2020
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Date
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all entries on or after June 15th, 2020
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Date
2019|2020 <2020-03
all entries in 2019 or 2020, and before March, 2020
Numeric
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all entries exactly matching 23
|
Numeric
23|24
all entries exactly matching 23 or 24
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Numeric
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all entries not exactly matching 23
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Numeric
<23
all entries lower than 23
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Numeric
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all entries lower than, or equal to, 23
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Numeric
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Numeric
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all entries higher than, or equal to, 23
combination
Numeric
>=20 <30 !23
all entries with values from 20 to 29, but not equal to 23
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all entries containing 'Asian', 'asian', including 'Caucasian', 'caucasian', etc.
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all entries containing 'Asian' but not containing 'Caucasian'
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all entries containing 'Asian' or 'African', but not containing 'Caucasian'
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all entries containing 'South Asian', but not containing 'South East Asian'
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95 entries on 1 page. Showing entries 1 - 95.
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Legend
How to query
Phenotype ID
Diagnosis/Initial
Diagnosis/Definite
Phenotype details
Inheritance
Age/Examination
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000117420
ataxia, spastic
-
hearing loss
Familial, autosomal recessive
-
-
-
-
Bernard Brais
00144686
0000117421
ataxia, spastic
-
hearing loss
Familial, autosomal recessive
-
-
-
-
Bernard Brais
00144687
0000117426
ataxia, spastic
-
-
Familial, autosomal recessive
-
-
-
-
Bernard Brais
00144692
0000117427
ataxia, spastic
-
-
Familial, autosomal recessive
-
-
-
-
Bernard Brais
00144693
0000117428
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144694
0000117429
ataxia, spastic
-
-
Isolated (sporadic)
-
-
-
-
Bernard Brais
00144695
0000117434
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144700
0000117435
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144701
0000117449
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144715
0000117450
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144716
0000117451
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144717
0000117452
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144718
0000117453
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144719
0000117462
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144728
0000117463
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144729
0000117464
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144730
0000117465
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144731
0000117466
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144732
0000117467
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144733
0000117468
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144734
0000117470
ataxia, spastic
-
-
Familial, autosomal recessive
-
-
-
-
Bernard Brais
00144736
0000117471
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144737
0000117473
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144739
0000117475
ataxia, spastic
-
-
Familial, autosomal recessive
-
-
-
-
Bernard Brais
00144741
0000117476
ataxia, spastic
-
histology FP
Familial, autosomal recessive
-
-
-
-
Bernard Brais
00144742
0000117479
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144745
0000117483
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144749
0000117484
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144750
0000117485
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144751
0000117486
ataxia, spastic
-
-
Isolated (sporadic)
-
-
-
-
Bernard Brais
00144752
0000117487
ataxia, spastic
-
-
Familial, autosomal recessive
-
-
-
-
Bernard Brais
00144753
0000117488
ataxia, spastic
-
-
Familial, autosomal recessive
-
-
-
-
Bernard Brais
00144754
0000117491
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144757
0000117493
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144759
0000117498
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144764
0000117499
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144765
0000117500
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144766
0000117502
ataxia, spastic
-
-
Familial, autosomal recessive
-
-
-
-
Bernard Brais
00144768
0000117507
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144773
0000117508
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144774
0000117509
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144775
0000117512
ataxia, spastic
-
-
Unknown
-
2y
-
-
Bernard Brais
00144778
0000117513
ataxia, spastic
-
-
Unknown
-
2y
-
-
Bernard Brais
00144779
0000117514
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144780
0000117516
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144782
0000117524
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144790
0000117527
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144793
0000117531
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144797
0000117532
ataxia, spastic
-
early onset
Unknown
-
-
-
-
Bernard Brais
00144798
0000117533
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144799
0000117535
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144801
0000117536
ataxia, spastic
-
-
Isolated (sporadic)
-
-
-
-
Bernard Brais
00144802
0000117540
ataxia, spastic
ataxia, spastic, Charlevoix-Saguenay type, autosomal recessive (ARSACS)
no leg spasticity
Unknown
-
-
-
-
Bernard Brais
00144806
0000117542
ataxia, spastic
-
-
Familial, autosomal recessive
-
-
-
-
Bernard Brais
00144808
0000117547
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144813
0000117549
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144815
0000117550
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144816
0000117551
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144817
0000117553
ataxia, spastic
-
-
Isolated (sporadic)
-
-
-
-
Bernard Brais
00144819
0000117554
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144820
0000117557
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144823
0000117558
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144824
0000117562
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144828
0000117563
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144829
0000117564
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144830
0000117572
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144838
0000117573
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144839
0000117574
ataxia, spastic
-
-
Familial, autosomal recessive
-
-
-
-
Bernard Brais
00144840
0000117576
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144842
0000117582
ataxia, spastic
-
-
Familial, autosomal recessive
-
-
-
-
Bernard Brais
00144848
0000117583
ataxia, spastic
-
-
Familial, autosomal recessive
-
-
-
-
Bernard Brais
00144849
0000117584
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144850
0000117586
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144852
0000117588
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144854
0000117589
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144855
0000117590
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144856
0000117591
ataxia, spastic
-
-
Familial, autosomal recessive
-
-
-
-
Bernard Brais
00144857
0000117600
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144866
0000117603
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144869
0000117604
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144870
0000117606
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144872
0000117607
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144873
0000117608
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144874
0000117609
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144875
0000117611
ataxia, spastic
-
-
Isolated (sporadic)
-
-
-
-
Bernard Brais
00144877
0000117615
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144881
0000117616
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144882
0000117617
ataxia, spastic
-
-
Unknown
-
-
-
-
Bernard Brais
00144883
0000119162
progressive spastic ataxia
-
progressive spastic ataxia and sensory motor peripheral neuropathy resembling a sacsinopathy
Isolated (sporadic)
23y
04y
-
-
Fabiana Fattori
00146422
0000132919
Spastic ataxia with mild ID
-
Gait instability, chorea, dysarthria
Familial, autosomal recessive
31y
02y
-
-
Inge Meijer
00168054
0000135700
-
-
Gait instability, chorea, dysarthria, Mild Intellectual Disability, Dystonia
Familial, autosomal recessive
-
02y
-
-
Inge Meijer
00170838
0000135701
-
-
Gait instability, Mild Intellectual Disability
Familial, autosomal recessive
-
04y?
-
-
Inge Meijer
00170842
0000138579
Spastic Ataxia
-
Gait and speech difficulties, Saccadic pursuit, UL & LL ataxia, LL spasticity, wheelchair, Normal cognitive state
Familial, autosomal recessive
-
20y
-
-
Inge Meijer
00170838
0000139685
Spastic ataxia
-
Delayed walking, spastic gait
Familial, autosomal recessive
-
<05y
-
-
Inge Meijer
00174860
0000141811
Spastic Ataxia
-
Delayed walking, abnormal gait, Cervical Dystonia
Familial, autosomal recessive
-
<03y
-
-
Inge Meijer
00176992
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