Global Variome shared LOVD
TBX4 (T-box 4)
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Phenotypes for disease #00556 (NS6 (Noonan syndrome, type 6 (NS-6)), OMIM:613224)
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
Example
Matches
Text
Arg
all entries containing 'Arg'
space
Text
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|
Text
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!
Text
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all entries not containing 'fs'
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Text
^p.(Arg
all entries beginning with 'p.(Arg'
$
Text
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all entries ending with 'Ser)'
=""
Text
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Text
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Text
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combination
Text
*|Ter !fs
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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
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Date
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all entries before the year 2020
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Date
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all entries in or before June, 2020
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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
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
Asian
all entries containing 'Asian', 'asian', including 'Caucasian', 'caucasian', etc.
Asian !Caucasian
all entries containing 'Asian' but not containing 'Caucasian'
Asian|African !Caucasian
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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19 entries on 1 page. Showing entries 1 - 19.
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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
0000078849
...
-
-
Isolated (sporadic)
-
-
-
-
-
Christina Lissewski
00100620
0000078852
-
-
-
Isolated (sporadic)
-
-
-
-
-
Christina Lissewski
00100623
0000078853
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Christina Lissewski
00100624
0000078855
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Christina Lissewski
00100625
0000078856
-
-
-
Unknown
-
-
-
-
-
Christina Lissewski
00100626
0000078857
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Christina Lissewski
00100627
0000078858
-
-
-
Unknown
-
-
-
-
-
Christina Lissewski
00100628
0000078859
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Christina Lissewski
00100629
0000078860
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Christina Lissewski
00100630
0000078861
-
-
-
Isolated (sporadic)
-
-
-
-
-
Christina Lissewski
00100631
0000078862
-
-
-
Unknown
-
-
-
-
-
Christina Lissewski
00100632
0000078863
-
-
-
Unknown
-
-
-
-
-
Christina Lissewski
00100633
0000078864
-
-
-
Unknown
-
-
-
-
-
Christina Lissewski
00100634
0000078865
-
-
-
Unknown
-
-
-
-
-
Christina Lissewski
00100634
0000078866
-
-
-
Unknown
-
-
-
-
-
Christina Lissewski
00100635
0000078867
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Christina Lissewski
00100636
0000078868
-
-
-
Unknown
-
-
-
-
-
Christina Lissewski
00100637
0000078869
-
-
-
Isolated (sporadic)
-
-
-
-
-
Christina Lissewski
00100638
0000078870
-
-
-
Isolated (sporadic)
-
-
-
-
-
Christina Lissewski
00100639
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