Global Variome shared LOVD
CREB3L2 (cAMP responsive element binding protein 3-...)
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Phenotypes for disease #00387 (ESCS (S-cone syndrome, enhanced (ESCS, Goldmann-Favre syndrome)), OMIM:268100)
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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Column type
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Matches
Text
Arg
all entries containing 'Arg'
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Text
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Text
Arg|Ser
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!
Text
!fs
all entries not containing 'fs'
^
Text
^p.(Arg
all entries beginning with 'p.(Arg'
$
Text
Ser)$
all entries ending with 'Ser)'
=""
Text
=""
all entries with this field empty
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Text
="p.0"
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all entries with this field not empty
!=""
Text
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combination
Text
*|Ter !fs
all entries containing '*' or 'Ter' but not containing 'fs'
Date
2020
all entries matching the year 2020
|
Date
2020-03|2020-04
all entries matching March or April, 2020
!
Date
!2020-03
all entries not matching March, 2020
<
Date
<2020
all entries before the year 2020
<=
Date
<=2020-06
all entries in or before June, 2020
>
Date
>2020-06
all entries after June, 2020
>=
Date
>=2020-06-15
all entries on or after June 15th, 2020
combination
Date
2019|2020 <2020-03
all entries in 2019 or 2020, and before March, 2020
Numeric
23
all entries exactly matching 23
|
Numeric
23|24
all entries exactly matching 23 or 24
!
Numeric
!23
all entries not exactly matching 23
<
Numeric
<23
all entries lower than 23
<=
Numeric
<=23
all entries lower than, or equal to, 23
>
Numeric
>23
all entries higher than 23
>=
Numeric
>=23
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
Some more advanced examples:
Example
Matches
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all entries containing 'Asian', 'asian', including 'Caucasian', 'caucasian', etc.
Asian !Caucasian
all entries containing 'Asian' but not containing 'Caucasian'
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all entries containing 'Asian' or 'African', but not containing 'Caucasian'
"South Asian"
all entries containing 'South Asian', but not containing 'South East Asian'
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70 entries on 1 page. Showing entries 1 - 70.
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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
0000026152
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032723
0000026153
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032724
0000026154
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032725
0000026155
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032726
0000026156
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032727
0000026157
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032728
0000026158
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032729
0000026159
Goldmann-Favre syndrome
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032730
0000026162
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032733
0000026163
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032734
0000026164
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032735
0000026165
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032736
0000026166
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032737
0000026167
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032738
0000026168
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032739
0000026169
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032740
0000026170
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032741
0000026171
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032742
0000026172
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032743
0000026173
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032744
0000026174
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032745
0000026175
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032746
0000026176
Goldmann-Favre syndrome
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032747
0000026177
Goldmann-Favre syndrome
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032748
0000026178
Goldmann-Favre syndrome
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032749
0000026184
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032755
0000026185
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032756
0000026186
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032757
0000026187
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032758
0000026188
Goldmann-Favre syndrome
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032759
0000026189
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032760
0000026190
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032761
0000026191
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032762
0000026192
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032763
0000026193
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032764
0000026195
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032766
0000026196
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032767
0000026198
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032769
0000026199
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032770
0000026200
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032771
0000026202
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032773
0000026203
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032774
0000026208
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032779
0000026209
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032780
0000026210
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032781
0000026211
Goldmann-Favre syndrome
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032782
0000026212
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032783
0000026213
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032784
0000026214
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032785
0000026215
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032786
0000026216
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032787
0000026217
Goldmann-Favre syndrome
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032788
0000026218
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032789
0000026264
helicoid subretinal fibrosis
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032835
0000026268
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00032839
0000027046
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00033617
0000027047
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00033618
0000027048
Goldmann-Favre syndrome
-
-
Unknown
-
-
-
-
-
Pascal Escher
00033619
0000027049
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00033620
0000027050
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00033621
0000027051
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00033622
0000027053
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00033624
0000027054
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00033625
0000027055
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00033626
0000027056
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00033627
0000027057
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00033628
0000027065
-
-
-
Unknown
-
-
-
-
-
Pascal Escher
00033636
0000082909
-
-
-
Familial, autosomal recessive
-
-
-
-
-
Marta de Castro-Miró
00105017
0000128007
-
enhanced S-cone syndrome
-
Familial, autosomal recessive
-
-
-
-
-
Dror Sharon
00155507
0000128011
-
enhanced S-cone syndrome
-
Familial, autosomal recessive
-
-
-
-
-
Dror Sharon
00155511
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