Global Variome shared LOVD
SLC25A22 (solute carrier family 25 (mitochondrial ...))
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Phenotypes for disease #01316 (EDM1 (dysplasia, epiphyseal, multiple, type 1 (EDM-1)), OMIM:132400)
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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Text
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space
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Text
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Text
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all entries not containing 'fs'
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Text
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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
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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
>
Date
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all entries after June, 2020
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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
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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24 entries on 1 page. Showing entries 1 - 24.
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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
0000186999
mild
-
-
Familial
-
-
-
-
-
LOVD
00247807
0000187000
severe
-
-
Unknown
-
-
-
-
-
Michael Briggs
00247822
0000187002
Fairbank
-
-
Unknown
-
-
-
-
-
LOVD
00247837
0000187014
ribbing
-
-
Familial
-
-
-
-
-
LOVD
00247864
0000187015
Fairbank
-
-
Isolated (sporadic)
-
-
-
-
-
LOVD
00247865
0000187017
Fairbank
-
-
Isolated (sporadic)
-
-
-
-
-
LOVD
00247867
0000187021
Fairbank
-
-
Isolated (sporadic)
-
-
-
-
-
LOVD
00247871
0000187024
ribbing
-
-
Familial
-
-
-
-
-
LOVD
00247874
0000187025
Fairbank
-
-
Familial
-
-
-
-
-
LOVD
00247875
0000187026
severe
-
-
Unknown
-
-
-
-
-
Michael Briggs
00247921
0000187032
atypical
-
-
Unknown
-
-
-
-
-
Michael Briggs
00247934
0000187033
atypical
-
-
Familial
-
-
-
-
-
Michael Briggs
00247937
0000187034
atypical
-
-
Unknown
-
-
-
-
-
Michael Briggs
00247985
0000187035
-
-
-
Unknown
-
-
-
-
-
Michael Briggs
00247930
0000187036
-
-
-
Unknown
-
-
-
-
-
Michael Briggs
00247944
0000187043
-
-
-
Familial
-
-
-
-
-
Michael Briggs
00247978
0000187044
-
-
-
Familial
-
-
-
-
-
Michael Briggs
00247984
0000187046
-
-
-
Familial
-
-
-
-
-
Michael Briggs
00247987
0000187048
-
-
-
Familial
-
-
-
-
-
Michael Briggs
00247820
0000187050
-
-
-
Familial
-
-
-
-
-
LOVD
00247858
0000187051
-
-
-
Familial
-
-
-
-
-
Michael Briggs
00247926
0000187052
-
-
-
Familial
-
-
-
-
-
Michael Briggs
00247936
0000187053
-
-
-
Familial
-
-
-
-
-
Michael Briggs
00247975
0000187054
-
-
-
Familial, autosomal dominant
-
-
-
-
-
LOVD
00247835
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