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Phenotypes for disease #01275 (DAR (Darier-White disease (DAR, keratosis follicularis)), OMIM:124200)
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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
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Text
Arg
all entries containing 'Arg'
space
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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
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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'
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363 entries on 4 pages. Showing entries 1 - 100.
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Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000041582
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00054927
0000041583
-
-
-
Isolated (sporadic)
-
-
-
-
-
Michel van Geel
00054928
0000041584
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00054929
0000041585
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00054930
0000041586
-
-
-
Unknown
-
-
-
-
-
Michel van Geel
00054931
0000041587
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00054932
0000041588
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00054933
0000041589
-
-
-
Isolated (sporadic)
-
-
-
-
-
Michel van Geel
00054934
0000041590
-
-
-
Isolated (sporadic)
-
-
-
-
-
Michel van Geel
00054935
0000041591
-
-
-
Unknown
-
-
-
-
-
Michel van Geel
00054936
0000041592
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00054937
0000041593
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00054938
0000041594
-
-
-
Isolated (sporadic)
-
-
-
-
-
Michel van Geel
00054939
0000041595
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00054940
0000041596
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00054941
0000041597
One patient with behaviour problem
-
-
Familial
-
-
-
-
-
Michel van Geel
00054942
0000041598
Bipolar I disorder
-
-
Unknown
-
-
-
-
-
Michel van Geel
00054943
0000041599
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00054944
0000041600
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00054945
0000041601
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00054946
0000041602
-
-
-
Unknown
-
-
-
-
-
Michel van Geel
00054947
0000041603
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00054948
0000041604
Learning difficulties 2x
-
-
Familial
-
-
-
-
-
Michel van Geel
00054949
0000041605
-
-
-
Isolated (sporadic)
-
-
-
-
-
Michel van Geel
00054950
0000041606
-
-
-
Isolated (sporadic)
-
-
-
-
-
Michel van Geel
00054951
0000041607
Tonic/clonic epilepsy, dysmorphic facies, low-normal IQ
-
-
Unknown
-
-
-
-
-
Michel van Geel
00054952
0000041608
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00054953
0000041609
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00054954
0000041610
-
-
-
Isolated (sporadic)
-
-
-
-
-
Michel van Geel
00054955
0000041611
-
-
-
Isolated (sporadic)
-
-
-
-
-
Michel van Geel
00054956
0000041612
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00054957
0000041613
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00054958
0000041614
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00054959
0000041615
-
-
-
Unknown
-
-
-
-
-
Michel van Geel
00054960
0000041616
-
-
-
Unknown
-
-
-
-
-
Michel van Geel
00054961
0000041617
-
-
-
Unknown
-
-
-
-
-
Michel van Geel
00054962
0000041618
-
-
-
Unknown
-
-
-
-
-
Michel van Geel
00054963
0000041619
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00054964
0000041620
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00054965
0000041621
One severe case, two flexural
-
-
Familial
-
-
-
-
-
Michel van Geel
00054966
0000041622
Multiple neuropsychiatric features
-
-
Familial
-
-
-
-
-
Michel van Geel
00054967
0000041623
-
-
-
Unknown
-
-
-
-
-
Michel van Geel
00054968
0000041624
Depression, family member committed suicide
-
-
Unknown
-
-
-
-
-
Michel van Geel
00054969
0000041625
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00054970
0000041626
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00054971
0000041627
Multiple neuropsychiatric features
-
-
Unknown
-
-
-
-
-
Michel van Geel
00054972
0000041628
One case has petit mal epilepsy
-
-
Familial
-
-
-
-
-
Michel van Geel
00054973
0000041629
Depression
-
-
Unknown
-
-
-
-
-
Michel van Geel
00054974
0000041630
-
-
-
Unknown
-
-
-
-
-
Michel van Geel
00054975
0000041631
Retinitis pigmentosa
-
-
Familial
-
-
-
-
-
Michel van Geel
00054976
0000041632
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00054977
0000041633
Learning difficulties
-
-
Unknown
-
-
-
-
-
Michel van Geel
00054978
0000041634
intellectual disability, schizophrenic
-
-
Unknown
-
-
-
-
-
Michel van Geel
00054979
0000041635
Myopathy during etretinate treatment
-
-
Familial
-
-
-
-
-
Michel van Geel
00054980
0000041636
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00054981
0000041637
Confluent cornifying lesions on arms and legs in one adult
-
-
Familial
-
-
-
-
-
Michel van Geel
00054982
0000041638
-
-
-
Unknown
-
-
-
-
-
Michel van Geel
00054983
0000041639
acral hemorrhagic
-
-
Familial
-
-
-
-
-
Michel van Geel
00054984
0000041640
Haemorrhagic
-
-
Familial
-
-
-
-
-
Michel van Geel
00054985
0000041641
Haemorrhagic
-
-
Familial
-
-
-
-
-
Michel van Geel
00054986
0000041642
Haemorrhagic
-
-
Unknown
-
-
-
-
-
Michel van Geel
00054987
0000041643
-
-
-
Unknown
-
-
-
-
-
Michel van Geel
00054988
0000041644
-
-
-
Unknown
-
-
-
-
-
Michel van Geel
00054989
0000041645
Cyclothymic disorder, hypertension
-
-
Unknown
-
-
-
-
-
Michel van Geel
00054990
0000041646
-
-
-
Unknown
-
-
-
-
-
Michel van Geel
00054991
0000041647
-
-
-
Unknown
-
-
-
-
-
Michel van Geel
00054992
0000041648
Mild intellectual disability
-
-
Unknown
-
-
-
-
-
Michel van Geel
00054993
0000041649
-
-
-
Unknown
-
-
-
-
-
Michel van Geel
00054994
0000041650
Schizoid personality psychosis, NOS, dysmorphic facies, epilepsy (age 1-7 yrs)
-
-
Unknown
-
-
-
-
-
Michel van Geel
00054995
0000041651
Type I segmental Darier disease
-
-
Isolated (sporadic)
-
48y
11y
-
-
Michel van Geel
00054996
0000041652
Type I segmental darier disease
-
-
Isolated (sporadic)
-
35y
17y
-
-
Michel van Geel
00054997
0000041653
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00054998
0000041654
Behavioral problems
-
-
Familial
-
-
-
-
-
Michel van Geel
00054999
0000041655
suicide in family, emotional problems
-
-
Familial
-
-
-
-
-
Michel van Geel
00055000
0000041656
Schizophrenia, seizures, depression
-
-
Familial
-
-
-
-
-
Michel van Geel
00055001
0000041657
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00055002
0000041658
Depression
-
-
Familial
-
-
-
-
-
Michel van Geel
00055003
0000041659
-
-
-
Isolated (sporadic)
-
-
-
-
-
Michel van Geel
00055004
0000041660
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00055005
0000041661
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00055006
0000041662
-
-
-
Isolated (sporadic)
-
65y
>10y
-
-
Michel van Geel
00055007
0000041663
-
-
-
Isolated (sporadic)
-
76y
50y
-
-
Michel van Geel
00055008
0000041664
-
-
-
Isolated (sporadic)
-
65y
>30y
-
-
Michel van Geel
00055009
0000041665
-
-
-
Familial
-
70y
20y
-
-
Michel van Geel
00055010
0000041666
-
-
-
Unknown
-
-
-
-
-
Michel van Geel
00055011
0000041667
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00055012
0000041668
-
-
-
Isolated (sporadic)
-
-
-
-
-
Michel van Geel
00055013
0000041669
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00055014
0000041670
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00055015
0000041671
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00055016
0000041672
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00055017
0000041674
Type I segmental manifistation left side trunk
-
-
Isolated (sporadic)
-
41y
38y
-
-
Michel van Geel
00055019
0000041675
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00055020
0000041676
-
-
-
Isolated (sporadic)
-
-
-
-
-
Michel van Geel
00055021
0000041677
-
-
-
Isolated (sporadic)
-
-
-
-
-
Michel van Geel
00055022
0000041678
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00055023
0000041679
-
-
-
Isolated (sporadic)
-
-
-
-
-
Michel van Geel
00055024
0000041680
-
-
-
Isolated (sporadic)
-
-
-
-
-
Michel van Geel
00055025
0000041681
-
-
-
Isolated (sporadic)
-
-
-
-
-
Michel van Geel
00055026
0000041682
-
-
-
Familial
-
-
-
-
-
Michel van Geel
00055027
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