Global Variome shared LOVD
IL1RN (interleukin 1 receptor antagonist)
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Phenotypes for disease #01378 (FHCL2 (hypercholesterolemia, familial, type 2 (FHCL2)), OMIM:144010)
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'
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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
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all entries with this field empty
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Text
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all entries exactly matching 'p.0'
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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
<=2020-06
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
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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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48 entries on 1 page. Showing entries 1 - 48.
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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
0000027168
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Ingrid Braenne
00033771
0000027169
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Ingrid Braenne
00033772
0000027170
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Ingrid Braenne
00033773
0000027171
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Benedikt Reiz
00033774
0000027172
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Ingrid Braenne
00033775
0000027173
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Benedikt Reiz
00033776
0000027174
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Ingrid Braenne
00033778
0000027175
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Ingrid Braenne
00033779
0000027176
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Ingrid Braenne
00033781
0000027177
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Benedikt Reiz
00033780
0000027178
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Ingrid Braenne
00033782
0000027179
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Mariana Kleinecke
00033777
0000027180
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Mariana Kleinecke
00033783
0000027181
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Ingrid Braenne
00033784
0000027182
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Ingrid Braenne
00033785
0000027183
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Benedikt Reiz
00033786
0000027184
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Mariana Kleinecke
00033787
0000027185
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Ingrid Braenne
00033788
0000027186
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Ingrid Braenne
00033789
0000027187
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Ingrid Braenne
00033789
0000027188
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Ingrid Braenne
00033790
0000027189
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Benedikt Reiz
00033791
0000027190
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Ingrid Braenne
00033792
0000027191
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Ingrid Braenne
00033793
0000027192
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Benedikt Reiz
00033768
0000027193
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Mariana Kleinecke
00033794
0000027194
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Benedikt Reiz
00033795
0000027195
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Benedikt Reiz
00033796
0000027196
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Benedikt Reiz
00033797
0000027197
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Mariana Kleinecke
00033798
0000027198
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Benedikt Reiz
00033799
0000027200
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Benedikt Reiz
00033800
0000027201
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Benedikt Reiz
00033801
0000027202
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Mariana Kleinecke
00033802
0000027203
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Benedikt Reiz
00033803
0000027204
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Benedikt Reiz
00033804
0000027205
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Benedikt Reiz
00033805
0000027206
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Mariana Kleinecke
00033806
0000027207
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Mariana Kleinecke
00033807
0000027213
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Ingrid Braenne
00033731
0000045429
-
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00058841
0000061403
-
-
-
Unknown
-
-
-
-
-
Jelena Čalyševa
00079911
0000082012
tendon Xanthomas(HP:0010874);Arcus Senilis (HP:0001084)
-
-
Familial, autosomal dominant
12y
12y
05y
Xanthomas
-
Nitika Setia
00104072
0000188413
hypercholesterolaemia with tendon xanthomas
-
-
Familial, autosomal dominant
-
-
-
-
-
Ellen Thomas
00249450
0000188482
-
-
-
Familial, autosomal dominant
-
58y
-
-
-
LOVD
00249570
0000188499
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Amanda Hooper
00249617
0000188500
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Amanda Hooper
00249618
0000188505
-
-
-
-
-
21y
-
-
-
LOVD
00249640
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