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Phenotypes for disease #05360 (RD (dermopathy, restrictive (RD)))
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.
Diagnosis/Initial
: initial diagnosis, before molecular testing
Diagnosis/Definite
: phenotype individual after molecular testing (OMIM abbreviation)
Phenotype details
: additional information on the phenotype of the individual, preferably use HPO terms only (http://www.human-phenotype-ontology.org/)
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/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'
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47 entries on 1 page. Showing entries 1 - 47.
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Legend
How to query
Phenotype ID
Diagnosis/Initial
Diagnosis/Definite
Phenotype details
Inheritance
Age/Examination
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000119218
-
-
-
Unknown
-
-
-
-
Johan den Dunnen
00146477
0000119219
-
-
-
Unknown
-
-
-
-
Johan den Dunnen
00146478
0000119220
-
-
-
Unknown
-
-
-
-
Johan den Dunnen
00146479
0000119221
-
-
-
Unknown
-
-
-
-
Johan den Dunnen
00146480
0000119224
-
-
-
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00146483
0000119225
-
-
-
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00146484
0000119248
-
-
thin, shiny skin exfoliating desquamation, small round open mouth, low-set ears, small pinched nose, joint contractures, distinctive pulmonic atelectasis
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00146507
0000119250
-
-
-
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00146509
0000119251
-
-
-
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00146510
0000119252
-
-
-
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00146511
0000119253
-
-
-
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00146512
0000119254
-
-
-
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00146513
0000119255
-
-
pregnancy growh retardation, short extremities, reduced movements, shrunken amninon membranes, absent clavicules, thin ribs, abnormal face; born 32nd week
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00146514
0000119258
-
-
still-born
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00146517
0000119259
-
-
-
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00146518
0000119260
-
-
IUGR, decreased fetal movements, polyhydramnios; delivery 32w-hypertelorism, down-slanting palpebral fissures, pinched nose, posterior rotated ears, micrognathia, O-position mouth, thin/rigid skin with erosions and scaling, prominent superficial vessels, multiple joints contractures, camptodactyly, absent and small nails, rocker-bottom feet, narrow chest
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00146519
0000119261
-
-
IUGR, decreased fetal movements, polyhydramnios; delivery 33w-hypertelorism, down-slanting palpebral fissures, pinched nose, posterior rotated ears, micrognathia, O-position mouth, thin/rigid skin with erosions and scaling, prominent superficial vessels, multiple joints contractures, camptodactyly, absent and small nails, rocker-bottom feet, narrow chest, thinned epidermal layers, focal hyperorthokeratosis, partial parakeratosis, immature/poorly developed hair follicles and sebaceous glands
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00146520
0000119262
-
-
4d-tight, translucent skin, prominent vessels, skin erosions, hypertelorism, antimongoloid axis, sparse eyelashes/eyebrows, pinched nose, natal teeth, microretrognathia and O-shaped mouth, multiple joint contractures, dysplastic clavicles, thin ribs; death from respiratuar distress
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00146521
0000119263
-
-
complete chorioamniotic membrane separation
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00146522
0000119264
-
-
-
Unknown
-
-
-
-
Johan den Dunnen
00146523
0000119266
-
-
-
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00146525
0000119267
-
-
-
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00146526
0000119270
-
-
-
Unknown
-
-
-
-
Tom Winder
00146529
0000119271
-
-
-
Unknown
-
-
-
-
Tom Winder
00146530
0000119272
-
-
-
Unknown
-
-
-
-
Tom Winder
00146531
0000119273
-
-
-
Unknown
-
-
-
-
Tom Winder
00146532
0000119275
-
-
born 32w; small eyes/nose, low set ears, open mouth; dolicocephalic head, open sutures, wide open anterior fontanelle; taut skin, parched and peeling, shallow respiration; joints/limbs stiff, movement restriction; chest X-ray dysplastic clavicles
Isolated (sporadic)
-
-
-
-
Parag Tamhankar
00146534
0000119276
-
-
terminated pregnancy (14-15w); no structural anomaly
Isolated (sporadic)
-
-
-
-
Parag Tamhankar
00146535
0000119277
-
-
30w-reduced fetal movements, polyhydramnios; 32w-progressive polyhydramnios, maternal distress, caesarean section delivery
Isolated (sporadic)
-
-
-
-
Parag Tamhankar
00146536
0000119278
-
-
33-34w-premature membrane rupture, meconium stained liquor, emergency caesarian section; tight dry and parched skin, small eyes/nose/mouth; joint contractures, fluid collections in scrotal sacs/subareolar region; chest X-ray hypoplastic clavicles
Isolated (sporadic)
-
-
-
-
Parag Tamhankar
00146537
0000119280
-
-
-
Familial, autosomal recessive
-
-
-
-
Claire Navarro
00146539
0000119281
-
-
-
Familial, autosomal recessive
-
-
-
-
Claire Navarro
00146540
0000119282
-
-
-
Familial, autosomal recessive
-
-
-
-
Claire Navarro
00146541
0000119283
-
-
-
Familial, autosomal recessive
-
-
-
-
Claire Navarro
00146542
0000119284
-
-
-
Familial, autosomal recessive
-
-
-
-
Claire Navarro
00146543
0000119286
-
-
-
Familial, autosomal recessive
-
-
-
-
Claire Navarro
00146545
0000119287
-
-
-
Familial, autosomal recessive
-
-
-
-
Claire Navarro
00146546
0000119288
-
-
-
Familial, autosomal recessive
-
-
-
-
Claire Navarro
00146547
0000119289
-
-
-
Familial, autosomal recessive
-
-
-
-
Claire Navarro
00146548
0000119290
-
-
-
Familial, autosomal recessive
-
-
-
-
Claire Navarro
00146549
0000119291
-
-
-
Familial, autosomal recessive
-
-
-
-
Claire Navarro
00146550
0000119292
-
-
-
Familial, autosomal recessive
-
-
-
-
Claire Navarro
00146551
0000119293
-
-
-
Familial, autosomal recessive
-
-
-
-
Claire Navarro
00146552
0000119294
-
-
-
Familial, autosomal recessive
-
-
-
-
Claire Navarro
00146553
0000164721
restrictive dermopathy
-
see paper
Isolated (sporadic)
-
0y
-
WB LMNA, LMNC and truncated
Johan den Dunnen
00216269
0000164740
restrictive dermopathy
-
<fetal movements; skin edematous, erosions, scleroderma-like lesions; blood vessels apparent under skin tibias, on trunk, skin taut, thick; nipples prominent, microretrognathism _+exophtalmia; mouth movements limited; X-ray clavicular hypoplasia
Isolated (sporadic)
-
0y
-
-
Johan den Dunnen
00216288
0000164959
restrictive dermopathy
-
-
Unknown
-
-
-
-
Tom Winder
00216507
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