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Phenotypes for disease #01612 (WHS (Wolf-Hirschhorn syndrome (WHS, 14p partial monosomy syndrome)), OMIM:194190)
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'
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23 entries on 1 page. Showing entries 1 - 23.
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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
0000124284
9m-onset seizures; no status epilepticus; no CNS complications; moderate developmental delay (DQ41), 2y3m-walking; height/weight (SD) -2.4/-2.0; oral feeding; no cleft lip/cleft palate; atrial septal defect; no urogenital defect; no skeletal abnormality; Strabismus; no hearing impairment;
Wolf-Hirschhorn syndrome
WHS
Isolated (sporadic)
6y
-
-
-
-
Johan den Dunnen
00151921
0000124285
2y6m-onset seizures; no status epilepticus; severe developmental delay (IQ23), 7y-walking; height/weight (SD) -5.4/-3.5; oral feeding; no cleft lip/cleft palate; atrial septal defect; Scoliosis (mild); no ophthalmologic abnormality; no hearing impairment; Multiple osteochondromatosis
Wolf-Hirschhorn syndrome
WHS
Isolated (sporadic)
13y
-
-
-
-
Johan den Dunnen
00151922
0000124286
1y3m-onset seizures; no status epilepticus; no CNS complications; severe developmental delay/no sitting; height/weight (SD) -5.3/-2.3; tube feeding; no cleft lip/cleft palate; no heart defect; no urogenital defect; no skeletal abnormality; no ophthalmologic abnormality; severe hearing impairment; hypercholesterolemia
Wolf-Hirschhorn syndrome
WHS
Isolated (sporadic)
1y8m
-
-
-
-
Johan den Dunnen
00151923
0000124287
7m-onset seizures; status epilepticus; Periventricular leukomalacia; severe developmental delay/no head control; height/weight (SD) -4.3/-3.0; tube feeding; no cleft lip/cleft palate; atrial septal defect, patent ductus arteriosus, ventricular septal defect; Limited hip flexion; Strabismus; moderate hearing impairment;
Wolf-Hirschhorn syndrome
WHS
Isolated (sporadic)
4y3m
-
-
-
-
Johan den Dunnen
00151924
0000124288
1y1m-onset seizures; no status epilepticus; moderate developmental delay, 4y-walking; height/weight (SD) -3.8/-2.9; oral feeding; no cleft lip/cleft palate; atrial septal defect; no skeletal abnormality; Strabismus; no hearing impairment; Hypercholesterolemia
Wolf-Hirschhorn syndrome
WHS
Isolated (sporadic)
5y10m
-
-
-
-
Johan den Dunnen
00151925
0000124289
2y1m-onset seizures; no status epilepticus; severe developmental delay, 7y-walking; height/weight (SD) -4.9/-3.0; oral feeding; no cleft lip/cleft palate; no heart defect; no urogenital defect; Strabismus (esotropia); no hearing impairment;
Wolf-Hirschhorn syndrome
WHS
Isolated (sporadic)
16y
-
-
-
-
Johan den Dunnen
00151926
0000124290
6m-onset seizures; status epilepticus; no CNS complications; severe developmental delay (IQ10), 7y-walking; height/weight (SD) -5.1/-2.5; oral feeding; no cleft lip/cleft palate; pulmonary stenosis; Renal hypoplasia, renal failure; Pes planus; no ophthalmologic abnormality; moderate hearing impairment; Hypercholesterolemia, hyperuricemia
Wolf-Hirschhorn syndrome
WHS
Isolated (sporadic)
18y
-
-
-
-
Johan den Dunnen
00151927
0000124291
7m-onset seizures; status epilepticus; severe developmental delay, 1y5m-roll over; height/weight (SD) -6.4/-3.7; tube feeding; no cleft lip/cleft palate; no heart defect; no urogenital defect; no skeletal abnormality; nasolacrimal duct obstruction; moderate hearing impairment; Fanconi syndrome due to valproate
Wolf-Hirschhorn syndrome
WHS
Isolated (sporadic)
6y6m
-
-
-
-
Johan den Dunnen
00151928
0000124292
10m-onset seizures; status epilepticus; no CNS complications; severe developmental delay, 12m-head control; height/weight (SD) -5.8/-4.1; oral feeding; no cleft lip/cleft palate; atrial septal defect, pulmonary stenosis; no urogenital defect; no skeletal abnormality; Strabismus; moderate hearing impairment;
Wolf-Hirschhorn syndrome
WHS
Isolated (sporadic)
5y3m
-
-
-
-
Johan den Dunnen
00151929
0000124293
no seizures; no status epilepticus; no CNS complications; severe developmental delay; height/weight (SD) -4.5/-3.9; tube feeding; cleft palate; patent ductus arteriosus; no urogenital defect; no skeletal abnormality; Right cataract; no hearing impairment;
Wolf-Hirschhorn syndrome
WHS
Isolated (sporadic)
7m
-
-
-
-
Johan den Dunnen
00151930
0000124294
6m-onset seizures; status epilepticus; no CNS complications; severe developmental delay (DQ10), 4y-sitting; height/weight (SD) -4.1/-3.3; tube feeding; submucous cleft palate; AR; no urogenital defect; Strabismus, nasolacrimal duct obstruction; no hearing impairment;
Wolf-Hirschhorn syndrome
WHS
Isolated (sporadic)
8y
-
-
-
-
Johan den Dunnen
00151931
0000124295
7m-onset seizures; status epilepticus; Ventricular enlargement; severe developmental delay, 2y-head contro; height/weight (SD) -11.7/-5.3; tube feeding; cleft lip/cleft palate; pulmonary stenosis; Renal hypoplasia, renal failure; Scoliosis (mild); Strabismus (exotropia); severe hearing impairment;
Wolf-Hirschhorn syndrome
WHS
Isolated (sporadic)
16y
-
-
-
-
Johan den Dunnen
00151932
0000124296
no seizures; no status epilepticus; no CNS complications; moderate developmental delay, 2y3m walking; height/weight (SD) -3.0/-2.3; tube feeding; no cleft lip/cleft palate; ventricular septal defect; no urogenital defect; no skeletal abnormality; no ophthalmologic abnormality; ;
Wolf-Hirschhorn syndrome
WHS
Isolated (sporadic)
12y
-
-
-
-
Johan den Dunnen
00151933
0000124297
9m-onset seizures; status epilepticus; no CNS complications; severe developmental delay, walking; height/weight (SD) -5.2/-4.0; oral feeding; ; atrial septal defect; no urogenital defect; no skeletal abnormality; no ophthalmologic abnormality; moderate hearing impairment;
Wolf-Hirschhorn syndrome
WHS
Isolated (sporadic)
5y
-
-
-
-
Johan den Dunnen
00151934
0000124298
8m-onset seizures; status epilepticus; Ventricular enlargement; severe developmental delay; height/weight (SD) -2.0/-2.3; oral feeding; no cleft lip/cleft palate; atrial septal defect, pulmonary stenosis; Criptorchidism; no skeletal abnormality; moderate hearing impairment;
Wolf-Hirschhorn syndrome
WHS
Isolated (sporadic)
9m
-
-
-
-
Johan den Dunnen
00151935
0000124299
9m-onset seizures; status epilepticus; hypoplasia corpus callosum, Cerebellar atrophy; severe developmental delay (DQ30), 9m-head control; height/weight (SD) –3.4/–2.7; tube feeding; submucous cleft palate; atrial septal defect, patent ductus arteriosus; Hydronephrosis; Talipes varus; Strabismus (exotropia), nasolacrimal duct obstruction; no hearing impairment;
Wolf-Hirschhorn syndrome
WHS
Isolated (sporadic)
1y11m
-
-
-
-
Johan den Dunnen
00151936
0000124300
1y-onset seizures; status epilepticus; hypoplasia corpus callosum; severe developmental delay (IQ10), 5y-walking; height/weight (SD) –5.3/–3.8; oral feeding; no cleft lip/cleft palate; atrial septal defect; Renal hypoplasia, renal failure; Acetabular dysplasia; Cataract; no hearing impairment; Hypercholesterolemia
Wolf-Hirschhorn syndrome
WHS
Isolated (sporadic)
18y
-
-
-
-
Johan den Dunnen
00151937
0000124301
1y2m-onset seizures; status epilepticus; no CNS complications; severe developmental delay/, head control; height/weight (SD) –5.6/–4.0; tube feeding; no cleft lip/cleft palate; atrial septal defect, pulmonary stenosis; Renal hypoplasia, renal failure; Sagittal craniosynostosis; Coloboma; no hearing impairment; Hypercholesterolemia
Wolf-Hirschhorn syndrome
WHS
Isolated (sporadic)
3y
-
-
-
-
Johan den Dunnen
00151938
0000124302
2m-onset seizures; status epilepticus; no CNS complications; severe developmental delay, no head control; height/weight (SD) –4.4/–2.4; tube feeding; no cleft lip/cleft palate; atrial septal defect, pulmonary stenosis; no urogenital defect; Scoliosis; Optic nerve atrophy; moderate hearing impairment;
Wolf-Hirschhorn syndrome
WHS
Isolated (sporadic)
2y11m
-
-
-
-
Johan den Dunnen
00151939
0000124303
1m-onset seizures; no status epilepticus; Cerebral atrophy; severe developmental delay, no head control; height/weight (SD) –3.3/–2.6; tube feeding; no cleft lip/cleft palate; patent ductus arteriosus, ventricular septal defect; Renal hypoplasia, vesicoureteric reflux; no skeletal abnormality; no ophthalmologic abnormality; moderate hearing impairment;
Wolf-Hirschhorn syndrome
WHS
Isolated (sporadic)
4y
-
-
-
-
Johan den Dunnen
00151940
0000124304
11m-onset seizures; status epilepticus; Cerebral atrophy; severe developmental delay; height/weight (SD) –2.3/–3.1; feeding gastrostomy; cleft palate; atrial septal defect, patent ductus arteriosus; ureteropelvic junction stenosis, renal failure; Talipes varus Cervical spine abnormalities; no ophthalmologic abnormality; severe hearing impairment;
Wolf-Hirschhorn syndrome
WHS
Isolated (sporadic)
2y10m
-
-
-
-
Johan den Dunnen
00151941
0000124305
2m-onset seizures; status epilepticus; HCC, Grey matter heterotopia, white matter volume loss; severe developmental delay (DQ10), no head control; height/weight (SD) –1.3/–1.4; feeding gastrostomy; no cleft lip/cleft palate; atrial septal defect; renal dysplasia, renal failure, cryptorchidism, hypospadias; no skeletal abnormality; Cataract, coloboma; severe hearing impairment;
Wolf-Hirschhorn syndrome
WHS
Isolated (sporadic)
6y
-
-
-
-
Johan den Dunnen
00151942
0000306884
Global developmental delay, Axial hypotonia, Failure to thrive, Microcephaly, Short stature, Retrognathia, Omphalocele, Elevated circulating creatine kinase concentration, Epicanthus
-
-
Unknown
-
-
-
-
-
Andreas Laner
00415083
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