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Phenotypes for disease #03945 (SLI (language impairment, specific (SLI)))
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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Date
2020
all entries matching the year 2020
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Date
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Date
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Date
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Date
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Date
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Date
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Date
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Numeric
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Numeric
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all entries exactly matching 23 or 24
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Numeric
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all entries not exactly matching 23
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Numeric
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all entries lower than 23
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Numeric
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all entries lower than, or equal to, 23
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Numeric
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Numeric
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combination
Numeric
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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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20 entries on 1 page. Showing entries 1 - 20.
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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
0000154479
Language impairment
PPVT and family history of language impairment
-
Familial, autosomal recessive
-
-
-
-
-
M. Hashim Raza
00206608
0000168017
Specific language impairment, PPVT affected
SLI
-
Familial, autosomal recessive
-
-
-
-
razam
M. Hashim Raza
00222897
0000170085
Specific Language Impairment, PPVT affected
SLI
-
Familial, autosomal recessive
-
-
-
-
razam
M. Hashim Raza
00223937
0000170086
Specific Language Impairment, PPVT affected
SLI
-
Familial, autosomal recessive
-
-
-
-
razam
M. Hashim Raza
00224970
0000170087
Specific Language Impairment, PPVT affected
SLI
-
Familial, autosomal recessive
-
-
-
-
-
M. Hashim Raza
00224971
0000170088
Specific Language Impairment, PPVT affected
SLI
-
Familial, autosomal recessive
-
-
-
-
razam
M. Hashim Raza
00224972
0000170089
Specific Language Impairment, PPVT affected
SLI
-
Familial, autosomal recessive
-
-
-
-
razam
M. Hashim Raza
00224973
0000170090
specific language impairment, Peabody picture vocabulary test affected
language impairment
-
Familial, autosomal recessive
-
-
-
-
-
M. Hashim Raza
00224974
0000171198
specific language impairment, PPVT affected
SLI
-
Familial, autosomal recessive
-
-
-
-
-
M. Hashim Raza
00226087
0000171200
specific language impairment, PPVT affected
SLI
-
Familial, autosomal recessive
-
-
-
-
-
M. Hashim Raza
00226089
0000171201
specific language impairment, PPVT affected
SLI
-
Familial, autosomal recessive
-
-
-
-
-
M. Hashim Raza
00226090
0000171202
specific language impairment, PPVT affected
SLI
-
Familial, autosomal recessive
-
-
-
-
-
M. Hashim Raza
00226091
0000201771
Specific language impairment (SLI)
language impairment
-
Familial
-
-
-
-
-
M. Hashim Raza
00263415
0000201774
Specific language impairment (SLI)
language impairment
-
Familial
-
-
-
-
-
M. Hashim Raza
00263418
0000201779
Specific language impairment (SLI)
-
-
Familial
-
-
-
-
-
M. Hashim Raza
00263423
0000201781
Specific language impairment (SLI)
-
-
Familial
-
-
-
-
-
M. Hashim Raza
00263425
0000201789
Specific language impairment (SLI)
-
-
Familial
-
-
-
-
-
M. Hashim Raza
00263433
0000280731
see paper; ..., all affected specific language impairment, special educational needs
specific language impairment
-
Unknown
-
-
-
-
-
Johan den Dunnen
00386932
0000350387
specific language impairment (HP:0002463)
language impairment
-
Familial, autosomal recessive
-
-
-
-
-
Sahib Kaloti
00464366
0000350390
specific language impairment (HP:0002463)
language impairment
-
Familial, autosomal dominant
-
-
-
-
-
Sahib Kaloti
00464368
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