Global Variome shared LOVD
C3orf17 (chromosome 3 open reading frame 17)
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Phenotypes for disease #01029 (KTCN (keratoconus (KTCN)))
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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Text
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Text
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all entries beginning with 'p.(Arg'
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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
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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
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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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15 entries on 1 page. Showing entries 1 - 15.
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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
0000067588
Keratoconus, atopic disease,celiac disease
-
-
Unknown
-
32
-
-
-
Andreas Laner
00088082
0000170075
-
keratoconus
-
Unknown
-
-
-
-
-
Rosemary Ekong
00224960
0000170077
-
keratoconus
TSC-2
Familial, autosomal dominant
-
-
-
-
-
Rosemary Ekong
00224962
0000170078
-
keratoconus
TSC-2
Familial, autosomal dominant
-
-
-
-
-
Rosemary Ekong
00224963
0000233329
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Tawfiq Froukh
00307908
0000233333
Keratoconus
-
-
Familial, autosomal recessive
-
-
-
-
-
Tawfiq Froukh
00307915
0000233334
Keratoconus
-
-
Familial, autosomal recessive
-
-
-
-
-
Tawfiq Froukh
00307913
0000233335
Keratoconus
-
-
Familial, autosomal dominant
-
-
-
-
-
Tawfiq Froukh
00307914
0000233336
Keratoconus
-
-
Familial, autosomal dominant
-
-
-
-
-
Tawfiq Froukh
00307912
0000233337
Keratoconus
-
-
Familial, autosomal dominant
-
-
-
-
-
Tawfiq Froukh
00307910
0000233338
Keratoconus
-
-
Familial, autosomal dominant
-
-
-
-
-
Tawfiq Froukh
00307911
0000281823
diopter right/left eye: -6.5/-5.25, corneal thickness right/left eye: 467/489
keratoconus
keratoconus
Familial, autosomal dominant
28y
21y
-
-
-
LOVD
00388268
0000281824
diopter right/left eye: -5.75/-11.5, corneal thickness right/left eye: 501/468
keratoconus
keratoconus
Familial, autosomal dominant
32y
25y
-
-
-
LOVD
00388269
0000281825
diopter right/left eye: -4.75/-9.5, corneal thickness right/left eye: 472/444
keratoconus
keratoconus
Familial, autosomal dominant
20y
15y
-
-
-
LOVD
00388270
0000341585
Keratoconus (HP:0000563), pectus excavatum (HP:0000767).
-
-
Unknown
76y
-
-
Keratoconus (HP:0000563) since early childhood.
-
Deepak Subramanian
00452942
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