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Phenotypes for disease #00339 (LRS (Larsen syndrome (LRS)), OMIM:150250)
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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Column type
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Matches
Text
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all entries containing 'Arg'
space
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|
Text
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!
Text
!fs
all entries not containing 'fs'
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Text
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all entries beginning with 'p.(Arg'
$
Text
Ser)$
all entries ending with 'Ser)'
=""
Text
=""
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Text
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Text
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all entries not exactly matching 'p.0?'
combination
Text
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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
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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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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
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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25 entries on 1 page. Showing entries 1 - 25.
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How to query
Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000061315
-
-
-
Unknown
-
-
-
-
-
Cynthia Silveira
00081548
0000186697
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247341
0000186698
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247342
0000186699
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247343
0000186702
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247352
0000186703
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247353
0000186716
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247399
0000186717
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247400
0000186718
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247401
0000186719
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247402
0000186720
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247403
0000186721
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247404
0000186722
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247405
0000186723
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247406
0000186724
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247407
0000186725
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247408
0000186726
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247409
0000186727
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247410
0000186728
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247411
0000186729
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247412
0000186730
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247413
0000186731
-
-
-
Isolated (sporadic)
-
-
-
-
-
Nils Koelling
00247415
0000186742
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247463
0000186743
-
-
-
Familial
-
-
-
-
-
Stephen Robertson
00247464
0000295561
congenital glaucoma, buphthalmos, palpebral edema, ecchymosis, corneal opacity, abnormality iris morphology, posterior vitreous detachment, Disproportionate short stature, hypotonia, patent foramen oval.
posterior vitreous detachment
Larsen syndrome
Familial, autosomal recessive
00y01m
-
-
abnormality iris morphology, buphthalmos
-
Miriam Erandi Reyna-Fabián
00402795
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