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Phenotypes for disease #05072 (WRWF (Wieacker-Wolff syndrome (WRWF)), OMIM:314580)
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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Column type
Example
Matches
Text
Arg
all entries containing 'Arg'
space
Text
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|
Text
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!
Text
!fs
all entries not containing 'fs'
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Text
^p.(Arg
all entries beginning with 'p.(Arg'
$
Text
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all entries ending with 'Ser)'
=""
Text
=""
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=""
Text
="p.0"
all entries exactly matching 'p.0'
!=""
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all entries with this field not empty
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Text
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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
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all entries before the year 2020
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Date
<=2020-06
all entries in or before June, 2020
>
Date
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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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35 entries on 1 page. Showing entries 1 - 35.
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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
0000174438
-
ZARD
-
Familial, X-linked dominant
-
-
-
-
-
Vera Kalscheuer
00234016
0000174439
-
ZARD
-
Familial, X-linked recessive
-
-
-
-
-
Vera Kalscheuer
00234017
0000174440
-
ZARD
-
Familial, X-linked recessive
-
-
-
-
-
Vera Kalscheuer
00234018
0000174441
-
ZARD
-
Familial, X-linked recessive
-
-
-
-
-
Vera Kalscheuer
00234019
0000174442
-
ZARD
-
Familial, X-linked recessive
-
-
-
-
-
Vera Kalscheuer
00234020
0000174443
-
ZARD
-
Familial, X-linked recessive
-
-
-
-
-
Vera Kalscheuer
00234021
0000174444
-
ZARD
-
Familial, X-linked dominant
-
-
-
-
-
Vera Kalscheuer
00234022
0000174445
-
ZARD
-
Familial, X-linked recessive
-
-
-
-
-
Vera Kalscheuer
00234023
0000174446
-
ZARD
-
Familial, X-linked dominant
-
-
-
-
-
Vera Kalscheuer
00234024
0000174447
-
ZARD
-
Familial, X-linked dominant
-
-
-
-
-
Vera Kalscheuer
00234025
0000174448
-
ZARD
-
Familial, X-linked dominant
-
-
-
-
-
Vera Kalscheuer
00234026
0000174449
-
ZARD
-
Familial, X-linked dominant
-
-
-
-
-
Vera Kalscheuer
00234027
0000174450
-
ZARD
-
Familial, X-linked dominant
-
-
-
-
-
Vera Kalscheuer
00234028
0000174451
-
ZARD
-
Familial, X-linked dominant
-
-
-
-
-
Vera Kalscheuer
00234029
0000174452
-
ZARD
-
Familial, X-linked dominant
-
-
-
-
-
Vera Kalscheuer
00234030
0000174453
-
ZARD
-
Familial, X-linked dominant
-
-
-
-
-
Vera Kalscheuer
00234031
0000174454
-
ZARD
-
Isolated (sporadic)
-
-
-
-
-
Vera Kalscheuer
00234032
0000174455
-
ZARD
-
Familial, X-linked recessive
-
-
-
-
-
Vera Kalscheuer
00234033
0000174456
-
ZARD
-
Familial, X-linked dominant
-
-
-
-
-
Vera Kalscheuer
00234034
0000174457
-
ZARD
-
Familial, X-linked dominant
-
-
-
-
-
Vera Kalscheuer
00234035
0000174458
-
ZARD
-
Familial, X-linked dominant
-
-
-
-
-
Vera Kalscheuer
00234036
0000174459
-
ZARD
-
Familial, X-linked dominant
-
-
-
-
-
Vera Kalscheuer
00234037
0000174460
-
ZARD
-
Isolated (sporadic)
-
-
-
-
-
Vera Kalscheuer
00234038
0000174462
dwarfism (HP:0001516) (2); long (flat) philtrum (HP:0000299) (2); oral motor dysfunction (HP:0005216) (1); low-set ears (HP:0000369) (2); ptosis (HP:0001488) (3); upturned nares (HP:0000463) (2); high-arched palate (HP:0000218) (2); carp-shaped mouth (HP:0010806) (2); drooling (HP:0002307) (3); short neck (with limited rotation) (HP:0000470) (2); neonatal respiratory distress (HP:0002643) (3); humeroscapular mobility restriction (HP:0006467) (2); narrow shoulders or thorax (HP:0006664) (3); poor feeding (HP:0002022) (4); kyphosis, lordosis or scoliosis (HP:0002751) (3); congenital hip dislocations or hip flexion contractures (HP:0001374) (4); flexion contractures of elbows or knees (HP:0002987, HP:0002978) (3); proximally placed thumbs (HP:0009623) (2); camptodactyly (HP:0001215) (5); ulnar deviation finger (HP:0009465) (3); proximally placed toes (HP:0001780) (4); equinovarus feet or contracture of Achilles tendon (HP:0008110, HP:0001771) (5); high anterior hairline (HP:0000294) (2); distal muscle weakness (HP:0002460) (2); edema or fat pads (hands and/or feet) (HP:0007514) (3); retardation of motor development (HP:0001263) (5); intellectual disability (HP:0001249) (5); spasticity (HP:0001257) (5); seizures (HP:0001250) (4); MRI delayed myelination (HP:0002188) (2); MRI diffuse cerebral atrophy (HP:0002283) (3)
arthrogryposis multiplex congenita, intellectual disability
WRWF
Familial, X-linked recessive
-
-
-
-
-
Johan den Dunnen
00234040
0000174463
equinovarus feet or contracture of Achilles tendon (HP:0008110, HP:0001771) (1)
arthrogryposis multiplex congenita, intellectual disability
WRWF
Familial, X-linked recessive
-
-
-
-
-
Johan den Dunnen
00234041
0000174464
dwarfism (HP:0001516) (1); long (flat) philtrum (HP:0000299) (5); ptosis (HP:0001488) (1); upturned nares (HP:0000463) (5); broad alveolar ridges (HP:0000187) (5); high-arched palate (HP:0000218) (5); carp-shaped mouth (HP:0010806) (5); short neck (with limited rotation) (HP:0000470) (1); neonatal respiratory distress (HP:0002643) (5); humeroscapular mobility restriction (HP:0006467) (1); kyphosis, lordosis or scoliosis (HP:0002751) (1); congenital hip dislocations or hip flexion contractures (HP:0001374) (2); short limbs (HP:0009826) (2); flexion contractures of elbows or knees (HP:0002987, HP:0002978) (2); proximally placed thumbs (HP:0009623) (1); camptodactyly (HP:0001215) (2); ulnar deviation finger (HP:0009465) (1); proximally placed toes (HP:0001780) (1); equinovarus feet or contracture of Achilles tendon (HP:0008110, HP:0001771) (2); high anterior hairline (HP:0000294) (5); edema or fat pads (hands and/or feet) (HP:0007514) (1); retardation of motor development (HP:0001263) (1); intellectual disability (HP:0001249) (1); seizures (HP:0001250) (1); MRI delayed myelination (HP:0002188) (1)
arthrogryposis multiplex congenita, intellectual disability
WRWF
Familial, X-linked recessive
-
-
-
-
-
Johan den Dunnen
00234042
0000174465
urine incontinence (HP:0000020) (1); distal muscle weakness (HP:0002460) (3); intellectual disability (HP:0001249) (3); dysarthria and/or deficit in expressive language (HP:0001260) (1); equinovarus feet or contracture of Achilles tendon (HP:0008110, HP:0001771) (3); camptodactyly (HP:0001215) (5)
arthrogryposis multiplex congenita, intellectual disability
WRWF
Familial, X-linked recessive
-
-
-
-
-
Johan den Dunnen
00234043
0000174466
drooling (HP:0002307) (2); equinovarus feet or contracture of Achilles tendon (HP:0008110, HP:0001771) (2); retardation of motor development (HP:0001263) (2); intellectual disability (HP:0001249) (2); spasticity (HP:0001257) (2); seizures (HP:0001250) (1);
arthrogryposis multiplex congenita, intellectual disability
WRWF
Familial, X-linked recessive
-
-
-
-
-
Johan den Dunnen
00234044
0000174467
intellectual disability (HP:0001249) (1)
arthrogryposis multiplex congenita, intellectual disability
WRWF
Familial, X-linked recessive
-
-
-
-
-
Johan den Dunnen
00234045
0000174469
intellectual disability (HP:0001249) (2)
arthrogryposis multiplex congenita, intellectual disability
WRWF
Familial, X-linked recessive
-
-
-
-
-
Johan den Dunnen
00234047
0000174470
dwarfism (HP:0001516) (1); long (flat) philtrum (HP:0000299) (1); oral motor dysfunction (HP:0005216) (1); low-set ears (HP:0000369) (1); ptosis (HP:0001488) (1); upturned nares (HP:0000463) (1); broad alveolar ridges (HP:0000187) (1); high-arched palate (HP:0000218) (1); carp-shaped mouth (HP:0010806) (1); drooling (HP:0002307) (1); short neck (with limited rotation) (HP:0000470) (1); neonatal respiratory distress (HP:0002643) (1); humeroscapular mobility restriction (HP:0006467) (1); narrow shoulders or thorax (HP:0006664) (1); poor feeding (HP:0002022) (1); kyphosis, lordosis or scoliosis (HP:0002751) (1); congenital hip dislocations or hip flexion contractures (HP:0001374) (1); short limbs (HP:0009826) (1); flexion contractures of elbows or knees (HP:0002987, HP:0002978) (1); proximally placed thumbs (HP:0009623) (1); camptodactyly (HP:0001215) (1); ulnar deviation finger (HP:0009465) (1); proximally placed toes (HP:0001780) (1); equinovarus feet or contracture of Achilles tendon (HP:0008110, HP:0001771) (1); high anterior hairline (HP:0000294) (1); distal muscle weakness (HP:0002460) (1); edema or fat pads (hands and/or feet) (HP:0007514) (1); retardation of motor development (HP:0001263) (1); intellectual disability (HP:0001249) (1); spasticity (HP:0001257) (1); seizures (HP:0001250) (1); MRI delayed myelination (HP:0002188) (1); MRI diffuse cerebral atrophy (HP:0002283) (1)
arthrogryposis multiplex congenita, intellectual disability
WRWF
Isolated (sporadic)
03y10m
-
-
-
-
Johan den Dunnen
00234048
0000174471
urine incontinence (HP:0000020) (1); distal muscle weakness (HP:0002460) (1); intellectual disability (HP:0001249) (1); dysarthria and/or deficit in expressive language (HP:0001260) (1); equinovarus feet or contracture of Achilles tendon (HP:0008110, HP:0001771) (1); camptodactyly (HP:0001215) (1)
arthrogryposis multiplex congenita, intellectual disability
WRWF
Isolated (sporadic)
9y
-
-
-
-
Johan den Dunnen
00234049
0000174472
urine incontinence (HP:0000020) (1); distal muscle weakness (HP:0002460) (1); intellectual disability (HP:0001249) (1); dysarthria and/or deficit in expressive language (HP:0001260) (1); equinovarus feet or contracture of Achilles tendon (HP:0008110, HP:0001771) (1); camptodactyly (HP:0001215) (1)
arthrogryposis multiplex congenita, intellectual disability
WRWF
Isolated (sporadic)
13y
-
-
-
-
Johan den Dunnen
00234050
0000231987
-
-
-
Unknown
-
-
-
-
-
Sha Hong
00306143
0000308162
Global developmental delay, Expressive language delay, Hypotonia, Mild microcephaly
-
-
Unknown
-
-
-
-
-
Andreas Laner
00416442
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