Global Variome shared LOVD
ZAR1 (zygote arrest 1)
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Phenotypes for disease #04224 (STL (Stickler syndrome (STL)))
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
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
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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
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all entries in 2019 or 2020, and before March, 2020
Numeric
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all entries exactly matching 23
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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
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all entries lower than 23
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all entries lower than, or equal to, 23
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Numeric
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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' 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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93 entries on 1 page. Showing entries 1 - 93.
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Legend
How to query
Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000092622
-
-
-
Familial, autosomal dominant
35y
-
-
-
-
Mouna Barat-Houari
00117387
0000130106
HP:0004327 Abnormality of the vitreous humor HP:0000545 Myopia HP:0000110 Renal dysplasia
-
-
Familial, autosomal dominant
20y
-
-
-
-
Thomas Nixon
00155750
0000130107
HP:0000541 Retinal detachment HP:0000545 Myopia HP:0000407 Sensorineural hearing impairment HP:0011800 Midface retrusion HP:0000278 Retrognathia
Type 2 Stickler syndrome
Stickler syndrome
Familial, autosomal dominant
42y
42y
-
-
-
Thomas Nixon
00165221
0000130108
HP:0000541 Retinal detachment HP:0000545 Myopia HP:0000407 Sensorineural hearing impairment HP:0000278 Retrognathia
Type 2 Stickler syndrome
Stickler syndrome
Familial, autosomal dominant
41y
41y
-
-
-
Thomas Nixon
00165222
0000130109
HP:0000541 Retinal detachment HP:0000545 Myopia HP:0000407 Sensorineural hearing impairment HP:0011800 Midface retrusion HP:0000278 Retrognathia
Type 2 Stickler syndrome
Stickler syndrome
Familial, autosomal dominant
39y
-
-
-
-
Thomas Nixon
00165224
0000130110
HP:0004327 Abnormality of the vitreous humor HP:0000545 Myopia
-
-
Familial, autosomal dominant
20y
-
-
-
-
Thomas Nixon
00165225
0000187481
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Julia Lopez
00248495
0000218020
-
Stickler syndrome
type 2
Unknown
-
-
-
-
-
Julia Lopez
00281846
0000218021
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00281847
0000218022
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00281849
0000218023
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00281850
0000218024
-
Stickler syndrome
type 2
Unknown
-
-
-
-
-
Julia Lopez
00281852
0000218025
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00281857
0000218026
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00281860
0000218027
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00281866
0000218028
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00281870
0000218029
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00281874
0000218030
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00281876
0000218031
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00281877
0000218032
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00281879
0000218033
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00281884
0000218034
-
Stickler syndrome
type 2
Unknown
-
-
-
-
-
Julia Lopez
00281887
0000218035
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00281892
0000218036
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00281894
0000218037
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00281895
0000218038
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00281896
0000218039
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00281897
0000218040
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00281898
0000218041
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00281900
0000218042
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00281901
0000218043
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00281902
0000218044
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00281903
0000218045
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00281904
0000218046
-
Stickler syndrome
type 2
Unknown
-
-
-
-
-
Julia Lopez
00281905
0000218047
-
Stickler syndrome
type 2
Unknown
-
-
-
-
-
Julia Lopez
00281907
0000218048
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00282191
0000218049
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283192
0000218050
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283195
0000218051
-
Stickler syndrome
type 2
Unknown
-
-
-
-
-
Julia Lopez
00283196
0000218052
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283198
0000218053
-
Stickler syndrome, without eye involvement
-
Unknown
-
-
-
-
-
Julia Lopez
00283200
0000218054
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283203
0000218055
-
Stickler syndrome, without eye involvement
-
Unknown
-
-
-
-
-
Julia Lopez
00283204
0000218056
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Julia Lopez
00283207
0000218057
-
Stickler syndrome
type 3
Unknown
-
-
-
-
-
Julia Lopez
00283215
0000226948
-
-
-
Familial, autosomal recessive
02y
03y
-
-
-
Peter Sparber
00299638
0000236283
-
Stickler syndrome
Stickler syndrome
Unknown
-
-
-
-
-
Lucia Micale
00311014
0000258556
-
Stickler syndrome
Stickler syndrome
Familial, autosomal recessive
-
-
-
-
-
Barbara Vona
00363190
0000258557
-
Stickler syndrome
Stickler syndrome
Familial, autosomal recessive
-
-
-
-
-
Barbara Vona
00363191
0000258558
-
Stickler syndrome
Stickler syndrome
Familial, autosomal recessive
-
-
-
-
-
Barbara Vona
00363192
0000273597
HP:0030515, HP:0000639, HP:0000365, HP:0001263, HP:0000006, HP:0011003, HP:0000175, HP:0003196, HP:0004327, HP:0000519
Stickler syndrome
-
Familial, autosomal dominant
-
-
-
-
-
Jinu Han
00379743
0000308524
-
Stickler syndrome
-
Isolated (sporadic)
-
-
-
-
-
Lucia Micale
00417014
0000308525
-
Stickler syndrome
-
Familial, autosomal dominant
-
-
-
-
-
Lucia Micale
00417015
0000308527
-
Stickler syndrome
-
Isolated (sporadic)
-
-
-
-
-
Lucia Micale
00417017
0000308528
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Lucia Micale
00417018
0000308533
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Lucia Micale
00417023
0000308535
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Lucia Micale
00417025
0000308536
-
Stickler syndrome
-
Familial, autosomal dominant
-
-
-
-
-
Lucia Micale
00417026
0000308547
-
Stickler syndrome
-
Familial, autosomal dominant
-
-
-
-
-
Lucia Micale
00417037
0000308552
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Lucia Micale
00417042
0000308567
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Lucia Micale
00417057
0000308579
-
Stickler syndrome
-
Isolated (sporadic)
-
-
-
-
-
Lucia Micale
00417069
0000308589
-
Stickler syndrome
-
Isolated (sporadic)
-
-
-
-
-
Lucia Micale
00417079
0000308608
-
Stickler syndrome
-
Familial, autosomal dominant
-
-
-
-
-
Lucia Micale
00417098
0000308658
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Lucia Micale
00417148
0000322357
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Maria Pia Leone
00431788
0000322359
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Maria Pia Leone
00431790
0000322360
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Maria Pia Leone
00431791
0000322390
-
Stickler syndrome
-
Unknown
-
-
-
-
-
Maria Pia Leone
00431821
0000333351
-
-
-
Isolated (sporadic)
-
-
-
-
-
Kosei Hasegawa
00444096
0000333432
see paper; ...
Stickler syndrome
STL1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00444180
0000333433
see paper; ...
Stickler syndrome
STL1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00444181
0000333434
see paper; ...
Stickler syndrome
STL1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00444182
0000333435
see paper; ...
Stickler syndrome
STL1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00444183
0000333436
see paper; ...
Stickler syndrome
STL1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00444184
0000333437
see paper; ...
Stickler syndrome
STL1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00444185
0000333438
see paper; ...
Stickler syndrome
STL2
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00444186
0000333439
see paper; ...
Stickler syndrome
STL2
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00444187
0000333440
see paper; ...
Stickler syndrome/Pierre-Robin sequence
STL1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00444188
0000333441
see paper; ...
Stickler syndrome
STL1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00444189
0000333442
see paper; ...
Stickler syndrome
STL1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00444190
0000333443
see paper; ...
Stickler syndrome
STL1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00444191
0000333444
see paper; ...
Stickler syndrome
STL1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00444192
0000333445
see paper; ...
Stickler syndrome
STL1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00444193
0000333446
see paper; ...
Stickler syndrome
STL1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00444194
0000333447
see paper; ...
Stickler syndrome
STL1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00444195
0000333448
see paper; ...
Stickler syndrome
STL1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00444196
0000333449
see paper; ...
Stickler syndrome
STL1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00444197
0000333450
see paper; ...
Stickler syndrome
STL2
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00444198
0000333451
see paper; ...
Stickler syndrome
STL1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00444199
0000333452
see paper; ...
Stickler syndrome
STL2
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00444200
0000333453
see paper; ...
Stickler syndrome
STL1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00444201
0000333454
see paper; ...
Stickler syndrome
STL1
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00444202
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