Global Variome shared LOVD
LOVD v.3.0 Build 30b [
Current LOVD status
]
Register as submitter
|
Log in
View all genes
Create a new gene entry
View all transcripts
Create a new transcript information entry
View all variants
View all variants affecting transcripts
Create a new data submission
View active genomic custom columns
Enable more genomic custom columns
View all individuals
Create a new data submission
View active custom columns
Enable more custom columns
View all diseases
Create a new disease information entry
View available phenotype columns
View all screenings
Create a new data submission
View active custom columns
Enable more custom columns
Submit new data
Phenotypes for disease #01510 (KNDLRS (Kindler's syndrome (KNDLRS)), OMIM:173650)
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
All list views have search fields which can be used to search data. You can search for a complete word or you can search for a part of a search term. If you enclose two or more words in double quotes, LOVD will search for the combination of those words only exactly in the order you specify. Note that search terms are case-insensitive and that wildcards such as * are treated as normal text! For all options, like "and", "or", and "not" searches, or searching for prefixes or suffixes, see the table below.
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.
217 entries on 3 pages. Showing entries 1 - 100.
10 per page
25 per page
50 per page
100 per page
Legend
How to query
« First
Prev
1
2
3
Next
Last »
Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000186757
-
-
-
Familial, autosomal recessive
-
4y
-
-
-
LOVD
00247534
0000186758
Skin fragility; blisters; mucosal involvement
-
-
Isolated (sporadic)
-
5y
-
-
-
Hiram de Almeida
00247520
0000186759
-
-
-
Familial, autosomal recessive
-
15y
-
-
-
LOVD
00247519
0000186760
Trauma induced blisters,; Skin atrophy,; Photosensitivity,; Constipation;
-
-
Familial, autosomal recessive
-
15y
-
-
-
Leila Youssefian
00247629
0000186761
see paper; ...
-
-
Familial, autosomal recessive
-
22y
-
-
-
LOVD
00247523
0000186762
widespread pigmentary changes in her skin as well as photosensitivity and fragility of the skin and mucous membranes. The mucosal involvement led to an erosive stomatitis as well as esophageal, anal and vaginal stenoses, requiring surgical intervention.
-
-
Familial, autosomal recessive
-
28y
-
-
-
LOVD
00247551
0000186763
childhood atrophic and fragile hypo‐ and hyperpigmented skin, brachydactyly, syndactyly, nail dystrophy, dental caries; PatIII4 37y-invasive transitional cell carcinoma bladder
-
-
Familial, autosomal recessive
-
37y
-
-
-
LOVD
00247538
0000186765
-
-
-
-
-
?
-
-
-
LOVD
00247544
0000186766
-
-
-
-
-
?
-
-
-
LOVD
00247555
0000186767
-
-
-
-
-
?
-
-
-
LOVD
00247570
0000186768
-
-
-
-
-
?
-
-
-
LOVD
00247576
0000186769
-
-
-
-
-
?
-
-
-
LOVD
00247577
0000186770
-
-
-
-
-
?
-
-
-
LOVD
00247578
0000186771
-
-
-
-
-
?
-
-
-
LOVD
00247579
0000186772
-
-
-
-
-
?
-
-
-
LOVD
00247580
0000186773
-
-
-
-
-
?
-
-
-
LOVD
00247581
0000186774
-
-
-
-
-
?
-
-
-
LOVD
00247582
0000186775
-
-
-
-
-
?
-
-
-
LOVD
00247583
0000186776
-
-
-
-
-
?
-
-
-
LOVD
00247618
0000186777
-
-
-
-
-
?
-
-
-
LOVD
00247619
0000186778
-
-
-
-
-
?
-
-
-
LOVD
00247637
0000186779
-
-
-
-
-
?
-
-
-
LOVD
00247638
0000186780
-
-
-
-
-
?
-
-
-
LOVD
00247645
0000186781
-
-
-
-
-
?
-
-
-
LOVD
00247650
0000186782
-
-
-
-
-
?
-
-
-
LOVD
00247680
0000186783
-
-
-
-
-
?
-
-
-
LOVD
00247681
0000186784
-
-
-
-
-
?
-
-
-
LOVD
00247682
0000186785
-
-
-
-
-
?
-
-
-
LOVD
00247683
0000186786
-
-
-
-
-
?
-
-
-
LOVD
00247684
0000186787
-
-
-
-
-
10y
-
-
-
LOVD
00247536
0000186788
-
-
-
-
-
10y
-
-
-
LOVD
00247547
0000186789
-
-
-
-
-
10y
-
-
-
LOVD
00247599
0000186790
-
-
-
-
-
10y
-
-
-
LOVD
00247605
0000186791
-
-
-
-
-
10y
-
-
-
LOVD
00247625
0000186792
-
-
-
-
-
11y
-
-
-
LOVD
00247556
0000186793
-
-
-
-
-
11y
-
-
-
LOVD
00247612
0000186794
-
-
-
-
-
11y
-
-
-
LOVD
00247660
0000186795
-
-
-
-
-
11y
-
-
-
LOVD
00247663
0000186796
Trauma induced blisters; Poikiloderma; Skin atrophy; Photosensitivity; Esophageal stricture; Constipation; Severe desquamative gingivitis ; Acrokeratosis
-
-
Familial, autosomal recessive
-
12y
-
-
-
Leila Youssefian
00247550
0000186797
-
-
-
-
-
12y
-
-
-
LOVD
00247565
0000186798
-
-
-
-
-
13y
-
-
-
LOVD
00247563
0000186799
-
-
-
-
-
13y
-
-
-
LOVD
00247604
0000186800
-
-
-
-
-
13y
-
-
-
LOVD
00247611
0000186801
-
-
-
-
-
13y
-
-
-
LOVD
00247641
0000186802
trauma induced blisters; atrophy on the dorsal aspects of hands and feet, localized poikiloderma; photo sensitivity; mild webbing/sclerodermiform fingers; oral bleeding; dysphagia; no intestine symptoms; anal bleeding, fissures; urogenital stenosis; ectropion, keratitis; no epithelial skin cancer
Kindler syndrome
KNDLRS
Familial, autosomal recessive
14y
-
-
-
-
LOVD
00247636
0000186803
-
-
-
-
-
15y
-
-
-
LOVD
00247553
0000186804
-
-
-
-
-
15y
-
-
-
LOVD
00247564
0000186805
-
-
-
-
-
15y
-
-
-
LOVD
00247668
0000186806
-
-
-
-
-
16y
-
-
-
LOVD
00247527
0000186807
Well-differentiated squamous cell carcinoma of the right ankle at 16y
-
-
-
-
16y
-
-
-
LOVD
00247640
0000186808
-
-
-
-
-
16y
-
-
-
LOVD
00247678
0000186809
-
-
-
Familial, autosomal recessive
-
17y
-
-
-
LOVD
00247569
0000186810
-
-
-
-
-
17y
-
-
-
LOVD
00247596
0000186811
-
-
-
-
-
17y
-
-
-
LOVD
00247606
0000186812
no trauma induced blisters; atrophy on the dorsal aspects of hands and feet, localized poikiloderma; photo sensitivity; no webbing/pseudoainhum hands/feet; oral bleeding; esophageal stenosis, requiring frequent dilatations or surgery; no intestine symptoms; no anal symptoms; no urogenital symptoms; no ocular symptoms; no epithelial skin cancer
Kindler syndrome
KNDLRS
Familial, autosomal recessive
17y
-
-
-
-
LOVD
00247653
0000186813
-
-
-
-
-
17y
-
-
-
LOVD
00247679
0000186814
-
-
-
-
-
18y
-
-
-
LOVD
00247559
0000186815
-
-
-
-
-
18y
-
-
-
LOVD
00247597
0000186816
-
-
-
-
-
18y
-
-
-
LOVD
00247624
0000186817
-
-
-
-
-
18y
-
-
-
LOVD
00247672
0000186818
Squamous cell carcinoma of the hard palate at the age of 34y
-
-
-
-
19y
-
-
-
LOVD
00247595
0000186819
-
-
-
-
-
19y
-
-
-
LOVD
00247603
0000186820
Trauma induced blisters; Poikiloderma; Skin atrophy; Photosensitivity; Esophageal stricture;
-
-
Familial, autosomal recessive
-
19y
-
-
-
Leila Youssefian
00247634
0000186821
-
-
-
-
-
19y
-
-
-
LOVD
00247664
0000186822
-
-
-
-
-
19y
-
-
-
LOVD
00247677
0000186823
-
-
-
-
-
1m
-
-
-
LOVD
00247535
0000186824
-
-
-
-
-
1y
-
-
-
LOVD
00247608
0000186825
-
-
-
-
-
1y
-
-
-
LOVD
00247616
0000186826
-
-
-
-
-
20y
-
-
-
LOVD
00247560
0000186827
-
-
-
-
-
21y
-
-
-
LOVD
00247572
0000186828
-
-
-
-
-
21y
-
-
-
LOVD
00247643
0000186829
-
-
-
-
-
21y
-
-
-
LOVD
00247665
0000186830
-
-
-
-
-
22y
-
-
-
LOVD
00247598
0000186831
trauma induced blisters; atrophy on the dorsal aspects of hands and feet, localized poikiloderma; photo sensitivity; mild webbing/sclerodermiform fingers; oral bleeding; no esophageal symptoms; no intestine symptoms; no anal symptoms; no urogenital symptoms; ectropion; no epithelial skin cancer
Kindler syndrome
KNDLRS
Familial, autosomal recessive
22y
-
-
-
-
LOVD
00247674
0000186832
-
-
-
-
-
23y
-
-
-
LOVD
00247524
0000186833
-
-
-
-
-
23y
-
-
-
LOVD
00247622
0000186834
-
-
-
-
-
23y
-
-
-
LOVD
00247642
0000186835
trauma induced blisters; atrophy on the dorsal aspects of hands and feet, disseminated poikiloderma; photo sensitivity; mild webbing/sclerodermiform fingers; oral bleeding; no esophageal symptoms; colitis/diarhoea; anal stenosis; urogenital stenosis; ectropion; no epithelial skin cancer
Kindler syndrome
KNDLRS
Familial, autosomal recessive
23y
-
-
-
-
LOVD
00247658
0000186836
Trauma induced blisters; Poikiloderma; Skin atrophy; Photosensitivity; Esophageal stricture; Severe desquamative gingivitis ; Acrokeratosis;
-
-
Familial, autosomal recessive
-
23y
-
-
-
Leila Youssefian
00247670
0000186837
Trauma induced blisters; Poikiloderma; Skin atrophy; Photosensitivity; Esophageal stricture; Constipation; Severe desquamative gingivitis ; Acrokeratosis;
-
-
Familial, autosomal recessive
-
24y
-
-
-
Leila Youssefian
00247628
0000186838
Trauma induced blisters; Poikiloderma; Skin atrophy; Photosensitivity; Esophageal stricture; Constipation; Severe desquamative gingivitis ; Acrokeratosis
-
-
Familial, autosomal recessive
-
24y
-
-
-
Leila Youssefian
00247659
0000186839
-
-
-
-
-
25y
-
-
-
LOVD
00247525
0000186840
-
-
-
-
-
25y
-
-
-
LOVD
00247541
0000186841
-
-
-
-
-
26y
-
-
-
LOVD
00247552
0000186842
squamous cell carcioma of the lip at the age of 28y; Revertant mosaicism
-
-
Familial, autosomal recessive
-
27y
-
-
-
LOVD
00247561
0000186843
-
-
-
-
-
27y
-
-
-
LOVD
00247600
0000186844
no trauma induced blisters; atrophy on the dorsal aspects of hands and feet, localized poikiloderma; photo sensitivity; no webbing/pseudoainhum hands/feet; periodontitis/microstoma; dysphagia; no intestine symptoms; no anal symptoms; no urogenital symptoms; ectropion; no epithelial skin cancer
Kindler syndrome
KNDLRS
Familial, autosomal recessive
27y
-
-
-
-
LOVD
00247654
0000186845
-
-
-
-
-
28y
-
-
-
LOVD
00247531
0000186846
-
-
-
-
-
28y
-
-
-
LOVD
00247602
0000186847
-
-
-
-
-
28y
-
-
-
LOVD
00247630
0000186848
-
-
-
-
-
28y
-
-
-
LOVD
00247666
0000186849
-
-
-
-
-
2y
-
-
-
LOVD
00247558
0000186850
-
-
-
-
-
2y
-
-
-
LOVD
00247615
0000186851
no trauma induced blisters; atrophy on the dorsal aspects of hands and feet, localized poikiloderma; photo sensitivity; no webbing/pseudoainhum hands/feet; periodontitis/microstoma; dysphagia; no intestine symptoms; no anal symptoms; no urogenital symptoms; ectropion; no epithelial skin cancer
Kindler syndrome
KNDLRS
Familial, autosomal recessive
30y
-
-
-
-
LOVD
00247655
0000186852
-
-
-
-
-
30y
-
-
-
LOVD
00247667
0000186853
-
-
-
-
-
30y
-
-
-
LOVD
00247685
0000186854
-
-
-
-
-
32y
-
-
-
LOVD
00247532
0000186855
Trauma induced blisters; Poikiloderma; Skin atrophy; Photosensitivity; Esophageal stricture;
-
-
Familial, autosomal recessive
-
32y
-
-
-
Leila Youssefian
00247566
0000186856
Trauma induced blisters; Poikiloderma; Skin atrophy; Photosensitivity; Esophageal stricture; Severe desquamative gingivitis ;
-
-
Familial, autosomal recessive
-
32y
-
-
-
Leila Youssefian
00247621
0000186857
Trauma induced blisters; Poikiloderma; Skin atrophy; Photosensitivity; Esophageal stricture; Constipation; Severe desquamative gingivitis ; Acrokeratosis;
-
-
Familial, autosomal recessive
-
33y
-
-
-
Leila Youssefian
00247644
10 per page
25 per page
50 per page
100 per page
Legend
How to query
« First
Prev
1
2
3
Next
Last »
Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our
APIs
to retrieve data.
Powered by
LOVD v.3.0
Build 30b
LOVD software ©2004-2024
Leiden University Medical Center
Database contents © by their respective submitters and curators