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Phenotypes for disease #01445 (CWS1 (Cowden syndrome, type 1 (CWS1)), OMIM:158350)
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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Operator
Column type
Example
Matches
Text
Arg
all entries containing 'Arg'
space
Text
Arg Ser
all entries containing 'Arg' and 'Ser'
|
Text
Arg|Ser
all entries containing 'Arg' or 'Ser'
!
Text
!fs
all entries not containing 'fs'
^
Text
^p.(Arg
all entries beginning with 'p.(Arg'
$
Text
Ser)$
all entries ending with 'Ser)'
=""
Text
=""
all entries with this field empty
=""
Text
="p.0"
all entries exactly matching 'p.0'
!=""
Text
!=""
all entries with this field not empty
!=""
Text
!="p.0"
all entries not exactly matching 'p.0?'
combination
Text
*|Ter !fs
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
!2020-03
all entries not matching March, 2020
<
Date
<2020
all entries before the year 2020
<=
Date
<=2020-06
all entries in or before June, 2020
>
Date
>2020-06
all entries after June, 2020
>=
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'
To sort on a certain column, click on the column header or on the arrows. If that column is already selected to sort on, the sort order will be swapped. The column currently sorted on has a darker blue background color than the other columns. The up and down arrows next to the column name indicate the current sorting direction. When sorting on any field other than the default, LOVD will sort secondarily on the default sort column.
20 entries on 1 page. Showing entries 1 - 20.
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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
0000045620
melanoma (HP:0002861), trichilemmoma (HP:0012844), breast adenocarcinoma, no thyroid abormality (-HP:000082), glioblastoma (HP:0100843)
-
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00059031
0000045621
trichilemmoma (HP:0012844), no breast adenocarcinoma, thyroid follicular adenoma, no CNS abnormality
-
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00059032
0000045622
trichilemmoma (HP:0012844), no breast adenocarcinoma, thyroid multinodular Goiter, macrocephaly (HP:0000256)
-
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00059033
0000045623
trichilemmoma (HP:0012844), breast fibroadenoma/hamartoma, no thyroid abormality (-HP:000082), macrocephaly (HP:0000256) lehrmitte-Duclos
-
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00059034
0000045624
trichilemmoma (HP:0012844), breast adenocarcinoma, thyroid follicular carcinoma, no CNS abnormality
-
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00059035
0000052461
-
-
-
Unknown
-
-
-
-
-
Jean-Pierre Bayley
00072770
0000061485
typical mucocutaneous lesions, begnin thyroid lesions, hamartomas polys, glycogenic acanthosis, lipovascular lesions, macrocephaly (HP:0000256)
-
-
Familial, autosomal dominant
43y
-
-
43y
-
Michel Longy
00081841
0000061486
Typical mucocutaneous lesions, begnin thyroid lesions,begnin breast lesions,hamartomas polyps,glycogenic acanthosis, lipovascular lesions, macrocephaly, uterine fibromas
-
-
Familial, autosomal dominant
62y
-
-
62y
-
Michel Longy
00081842
0000144248
Cowden syndrome
-
-
Unknown
-
-
-
-
-
Stephanie Baert-Desurmont
00183544
0000144249
Cowden syndrome
-
-
Unknown
-
-
-
-
-
Stephanie Baert-Desurmont
00183545
0000144250
Cowden syndrome
-
-
Unknown
-
-
-
-
-
Stephanie Baert-Desurmont
00183546
0000144251
Cowden syndrome
-
-
Unknown
-
-
-
-
-
Stephanie Baert-Desurmont
00183547
0000144253
Cowden syndrome
-
-
Unknown
-
-
-
-
-
Stephanie Baert-Desurmont
00183549
0000144254
Cowden syndrome
-
-
Unknown
-
-
-
-
-
Stephanie Baert-Desurmont
00183550
0000144255
Cowden syndrome
-
-
Unknown
-
-
-
-
-
Stephanie Baert-Desurmont
00183551
0000144256
Cowden syndrome
-
-
Unknown
-
-
-
-
-
Stephanie Baert-Desurmont
00183552
0000144257
Cowden syndrome
-
-
Unknown
-
-
-
-
-
Stephanie Baert-Desurmont
00183553
0000144258
Cowden syndrome
-
-
Unknown
-
-
-
-
-
Stephanie Baert-Desurmont
00183554
0000274244
Macrocephaly, Abnormality of the face, Global developmental delay, Abnormal facial shape, Mild global developmental delay, Neurodevelopmental delay, Increased head circumference
-
-
Unknown
-
-
-
-
-
Andreas Laner
00380394
0000351561
Intellectual disability, Deafness, Macrocephaly, Cleft palate
-
-
Unknown
-
-
-
-
-
Juliana Mazzeu
00466174
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