Global Variome shared LOVD
SMARCD3 (SWI/SNF related, matrix associated, actin ...)
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Phenotypes for disease #05100 (UCMD (dystrophy, muscular, congenital, Ullrich (UCMD)))
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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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175 entries on 2 pages. Showing entries 1 - 100.
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Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000086210
-
-
-
Unknown
-
-
-
-
-
Alison Blain
00108736
0000086227
-
-
-
Isolated (sporadic)
-
-
-
-
-
Anne Lampe
00108754
0000086229
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00108756
0000086230
-
-
-
Isolated (sporadic)
-
-
-
-
-
Anne Lampe
00108757
0000086237
see paper; ..., mild
-
-
Isolated (sporadic)
-
-
-
-
-
Anne Lampe
00108764
0000086239
-
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00108766
0000086243
mild
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00108770
0000086244
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00108771
0000086245
mild
-
-
Isolated (sporadic)
-
-
-
-
-
Anne Lampe
00108772
0000086246
-
-
-
Isolated (sporadic)
-
-
-
-
-
Anne Lampe
00108773
0000086248
mild
-
-
Isolated (sporadic)
-
-
-
-
-
Anne Lampe
00108775
0000086252
-
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00108779
0000086253
-
-
-
Unknown
-
-
-
-
-
Anne Lampe
00108780
0000086254
-
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00108781
0000086255
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00108782
0000086256
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00108783
0000086257
-
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00108784
0000086259
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00108786
0000086260
mild
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00108787
0000086261
-
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00108788
0000086266
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00108793
0000086267
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00108794
0000086268
mild
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00108795
0000086269
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00108796
0000086270
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00108797
0000086272
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00108799
0000086274
-
-
-
Familial
-
-
-
-
-
Johan den Dunnen
00108801
0000086276
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00108803
0000086277
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00108804
0000086278
mild
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00108805
0000086279
mild
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00108806
0000086281
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00108808
0000086287
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00108814
0000086289
-
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00108816
0000086290
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00108817
0000086292
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00108819
0000086293
-
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00108820
0000086294
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00108821
0000086304
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00108831
0000086314
CPK normal
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00108841
0000086315
-
-
-
Familial
-
-
-
-
-
Johan den Dunnen
00108842
0000086316
CPK normal
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00108843
0000086322
-
-
-
Unknown
-
-
-
-
-
Tom Winder
00108849
0000086324
-
-
-
Unknown
-
-
-
-
-
Tom Winder
00108851
0000086325
-
-
-
Unknown
-
-
-
-
-
Tom Winder
00108852
0000086329
-
-
-
Unknown
-
-
-
-
-
Tom Winder
00108856
0000086330
-
-
-
Unknown
-
-
-
-
-
Tom Winder
00108857
0000086333
-
-
-
Unknown
-
-
-
-
-
Tom Winder
00108860
0000086336
proximall weakness; contractures; CPK ~400
-
-
Unknown
-
-
-
-
-
Tom Winder
00108863
0000086340
-
-
-
Unknown
-
-
-
-
-
Tom Winder
00108867
0000086341
-
-
-
Unknown
-
-
-
-
-
Tom Winder
00108868
0000086342
-
-
-
Unknown
-
-
-
-
-
Tom Winder
00108869
0000086343
-
-
-
Unknown
-
-
-
-
-
Tom Winder
00108870
0000086344
-
-
-
Unknown
-
-
-
-
-
Tom Winder
00108871
0000086346
-
-
-
Unknown
-
-
-
-
-
Tom Winder
00108873
0000086347
-
-
-
Unknown
-
-
-
-
-
Tom Winder
00108874
0000086348
-
-
-
Unknown
-
-
-
-
-
Tom Winder
00108875
0000086350
MRI-brain white matter lesions (numerous patchy); delayed motor skills; roll-6m, sit-12m, c-12m, walk-4y3m
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00108877
0000086352
-
-
-
Unknown
-
-
-
-
-
Tom Winder
00108879
0000086356
-
-
-
Unknown
-
-
-
-
-
Tom Winder
00108883
0000086357
-
-
-
Unknown
-
-
-
-
-
Tom Winder
00108884
0000086358
-
-
-
Unknown
-
-
-
-
-
Tom Winder
00108885
0000086362
-
-
-
Unknown
-
-
-
-
-
Tom Winder
00108889
0000086363
-
-
-
Unknown
-
-
-
-
-
Tom Winder
00108890
0000086365
-
-
-
Unknown
-
-
-
-
-
Tom Winder
00108892
0000086366
-
-
-
Unknown
-
-
-
-
-
Tom Winder
00108893
0000086369
-
-
-
Unknown
-
-
-
-
-
Tom Winder
00108896
0000086370
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Tom Winder
00108897
0000086373
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Tom Winder
00108900
0000086378
-
-
-
Unknown
-
-
-
-
-
Tom Winder
00108905
0000086381
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Tom Winder
00108908
0000086668
hypotonia, hyperextensible joints
-
-
Familial, autosomal recessive
-
-
-
-
-
Tom Winder
00109195
0000086669
part time wheelchair (8y); 7y-first wheelchair use; walk-24m; wheelchair-bound >8y
-
-
Isolated (sporadic)
-
-
-
-
-
Russell Butterfield
00109196
0000086673
intermediate; ambulatory with assistive devices (7y); wheelchair-bound >7y
-
-
Isolated (sporadic)
-
-
-
-
-
Russell Butterfield
00109200
0000086674
intermediate; walk-14m; wheelchair-bound >10y
-
-
Isolated (sporadic)
-
-
-
-
-
Russell Butterfield
00109201
0000086678
intermediate; ambulatory with assistive devices (4y); walk-24m; wheelchair-bound >4y
-
-
Isolated (sporadic)
-
-
-
-
-
Russell Butterfield
00109205
0000086679
intermediate; ambulatory with assistive devices (4y); walk-24m; wheelchair-bound >4y
-
-
Isolated (sporadic)
-
-
-
-
-
Russell Butterfield
00109206
0000086680
ambulatory with assistive devices (12y); 6y-first wheelchair use; walk-12m; wheelchair-bound 6y
-
-
Isolated (sporadic)
-
-
-
-
-
Russell Butterfield
00109207
0000086681
wheelchair-bound 15y
-
-
Unknown
-
-
-
-
-
Russell Butterfield
00109208
0000086682
intermediate; ambulatory with assistive devices (13y); 9y-first wheelchair use; walk-12m; wheelchair-bound 9y
-
-
Isolated (sporadic)
-
-
-
-
-
Russell Butterfield
00109209
0000086683
severe, early onset; never walked; wheelchair-bound 6y
-
-
Isolated (sporadic)
-
-
-
-
-
Russell Butterfield
00109210
0000086685
intermediate; first wheelchair use 9.5y; walk-18m; wheelchair-bound 13y
-
-
Isolated (sporadic)
-
-
-
-
-
Russell Butterfield
00109212
0000086691
intermediate; ambulatory with assistive devices (7y); walk-17m; wheelchair-bound >7y
-
-
Isolated (sporadic)
-
-
-
-
-
Russell Butterfield
00109218
0000086692
intermediate; ambulatory with assistive devices (10y); walk-17m; wheelchair-bound >10y
-
-
Isolated (sporadic)
-
-
-
-
-
Russell Butterfield
00109219
0000086693
wheelchair-bound 10y
-
-
Isolated (sporadic)
-
-
-
-
-
Russell Butterfield
00109220
0000086696
intermediate; part time wheelchair (23y); walk-20m; wheelchair-bound >23y
-
-
Isolated (sporadic)
-
-
-
-
-
Russell Butterfield
00109223
0000086699
intermediate; walk-14m; wheelchair-bound >7y
-
-
Isolated (sporadic)
-
-
-
-
-
Russell Butterfield
00109226
0000086702
intermediate; wheelchair-bound >12y
-
-
Isolated (sporadic)
-
-
-
-
-
Russell Butterfield
00109229
0000086704
intermediate; walk-13m; wheelchair-bound >10y
-
-
Familial, autosomal dominant
-
-
-
-
-
Russell Butterfield
00109231
0000086706
intermediate; ambulatory with assistive devices (41y); walk-24m; wheelchair-bound >41y
-
-
Isolated (sporadic)
-
-
-
-
-
Russell Butterfield
00109233
0000086707
ambulatory with assistive devices (9y); 8y-first wheelchair use; walk-16m; wheelchair-bound >9y
-
-
Isolated (sporadic)
-
-
-
-
-
Russell Butterfield
00109234
0000086715
intermediate; 14y-first wheelchair use; walk-12m; wheelchair-bound 15y
-
-
Isolated (sporadic)
-
-
-
-
-
Russell Butterfield
00109242
0000086717
first wheelchair use 8y; walk-18m; wheelchair-bound >8y
-
-
Isolated (sporadic)
-
-
-
-
-
Russell Butterfield
00109244
0000086719
intermediate; walk-15m; wheelchair-bound >27y
-
-
Isolated (sporadic)
-
-
-
-
-
Russell Butterfield
00109246
0000086722
intermediate; ambulatory with assistive devices (19y); wheelchair-bound >19y
-
-
Unknown
-
-
-
-
-
Russell Butterfield
00109249
0000086723
severe, early onset; never walked; wheelchair-bound 3y
-
-
Isolated (sporadic)
-
-
-
-
-
Russell Butterfield
00109250
0000086725
part time wheelchair (17y); 8y-first wheelchair use; walk-24m; wheelchair-bound >17y
-
-
Isolated (sporadic)
-
-
-
-
-
Russell Butterfield
00109252
0000086729
ambulatory with assistive devices (5y); walk-18m; wheelchair-bound >5y
-
-
Familial, autosomal recessive
-
-
-
-
-
Russell Butterfield
00109256
0000086733
intermediate; walk-18m; wheelchair-bound >7y
-
-
Unknown
-
-
-
-
-
Russell Butterfield
00109260
0000086734
intermediate; ambulatory with assistive devices (7y); walk-11m; wheelchair-bound >7y
-
-
Isolated (sporadic)
-
-
-
-
-
Russell Butterfield
00109261
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