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Phenotypes for disease #05262 (SGBS (Simpson-Golabi-Behmel syndrome (SGBS)))
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/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
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Text
Arg
all entries containing 'Arg'
space
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Arg Ser
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|
Text
Arg|Ser
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!
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"
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!=""
Text
!=""
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!=""
Text
!="p.0"
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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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59 entries on 1 page. Showing entries 1 - 59.
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How to query
Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000081794
Simpson–Golabi–Behmel syndrome; birth 36w, weight 3350g, length 50cm, OFC 35.5cm; Macrosomia (HP:0001520), Coarse face (HP:0000280), Macrocephaly (HP:0000256), Broad nasal bridge (HP:0000431), Macrostomia (HP:0000154), Macrognathia (HP:0000303), Thoracolumbar kyphosis (HP:0005619), ...
-
-
Unknown
06y
00y00m00d
-
-
Lynn Boekhoudt
00103754
0000081795
see paper; ...
-
-
Familial, X-linked recessive
<00y00m00d
-
-
-
Johan den Dunnen
00103756
0000081798
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Johan den Dunnen
00103877
0000081799
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Lynn Boekhoudt
00103758
0000081800
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Johan den Dunnen
00103757
0000081801
Simpson–Golabi–Behmel syndrome; birth 38w, weight 4410g, length 51cm, OFC 36.5cm; 27m (02y03m) weight 11.1kg, length 75cm, OFC 47cm; Congenital overgrowth (HP:0001548), Postnatal overgrowth (HP:0001548), Coarse face (HP:0000280), Macroglossia (HP:0000158), macrostomia (HP:0000154), Congenital heart defect (HP:0001627), Speech delay (HP:0000750), Intellectual disability (HP:0001249), ...
-
-
Unknown
02y03m
00y00m00d
-
-
Lynn Boekhoudt
00103232
0000081802
Pre- and postnatal overgrowth syndrome with intellectual disability and congenital malformations; ultrasonograph macrosomia (HP:0001520), polyhydramnios (HP:0001561); birth 27w weight 1400g, length 40cm, OFC 29cm; 02y10m weight 17,7kg, length 99cm, OFC 49.2cm; brachycephaly (HP:0000248), coarse face (HP:0000280), hypertelorism (HP:0000316), epicanthal folds (HP:0000286), short nose (HP:0003196), broad nasal bridge (HP:0000431), arched eyebrows (HP:0002553), macrostomia (HP:0000154), macroglossia (HP:0000158), midline furrow of the tongue (HP:0000221), prognathism (HP:0000303), sparse hair (HP:0008070), low-set posteriorly rotated ears (HP:0000368), pectus carinatum (HP:0000768), broad fingers (HP:0001500), toes with short nails (HP:0001799); X-ray broad shortened phalanges (HP:0009803, HP:0006009), delayed bone age (HP:0002750), ...
-
-
Familial, X-linked recessive
02y10m
00y00m00d
-
-
Lynn Boekhoudt
00103218
0000081803
pre- and postnatal overgrowth syndrome with intellectual disability and congenital malformations; birth 36w weight 3940g, length 54cm, OFC 35.5cm; 07y04m weight 34.3kg, length 138cm, OFC 55.3cm; Neurodevelopmental delay, delayed speech, coarse face (HP:0000280),hypertelorism (HP:0000316), short nose (HP:0003196), broad nasal bridge (HP:0000431), long philtrum (HP:0000343), macrostomia (HP:0000154), macroglossia (HP:0000158), midline furrow of the tongue (HP:0000221), prognathism (HP:0000303), arched bushy eyebrows (HP:0000574, HP:0002553), synophrys (HP:0000664), ...
-
-
Familial, X-linked recessive
07y04m
00y00m00d
-
-
Lynn Boekhoudt
00103225
0000081804
pre- and postnatal overgrowth syndrome with intellectual disability and congenital malformations; birth 37w weight 4010g, length 56cm, OFC 36 cm; 01y09m weight 15kg, length 89.3cm, OFC 50.5cm; coarse face (HP:0000280), hypertelorism (HP:0000316), epicanthal folds (HP:0000286), short nose (HP:0003196), broad nasal bridge (HP:0000431), prognatism (HP:0000303), macrostomia (HP:0000154), macroglossia (HP:0000158), downturned lower lip (HP:0000232), bifid uvula (HP:0000193), low-set posteriorly rotated ears (HP:0000368), arched eyebrows (HP:0002553)
-
-
Familial, X-linked recessive
01y09m
00y00m00d
-
-
Lynn Boekhoudt
00103223
0000086064
see paper; ...
-
-
Unknown
-
-
-
-
Marie-Laure Vuillaume
00108468
0000092386
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117142
0000092387
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117143
0000092388
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117144
0000092389
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117145
0000092390
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117146
0000092391
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117147
0000092392
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117148
0000092393
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117149
0000092394
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117150
0000092395
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117151
0000092396
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117152
0000092397
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117153
0000092398
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117154
0000092399
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117155
0000092400
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117156
0000092401
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117157
0000092402
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117158
0000092403
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117159
0000092404
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117160
0000092405
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117161
0000092406
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117162
0000092407
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117163
0000092408
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117164
0000092409
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117165
0000092410
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117166
0000092411
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117167
0000092412
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117168
0000092413
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117169
0000092414
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117170
0000092415
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117171
0000092416
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117172
0000092417
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117173
0000092418
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117174
0000092419
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117175
0000092420
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117176
0000092421
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117177
0000092422
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117178
0000092423
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117179
0000092424
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117180
0000092425
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117181
0000092426
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117182
0000092427
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117183
0000092428
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117184
0000092429
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117185
0000092430
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117186
0000092431
see paper; ...
-
-
Familial, X-linked recessive
-
-
-
-
Marie-Laure Vuillaume
00117187
0000092432
see paper; ...
-
-
Familial, X-linked
-
-
-
-
Marie-Laure Vuillaume
00111171
0000279733
-
-
Simpson-Golabi-Behmel (SGBS) syndrome
Familial, X-linked
-
-
-
-
Sander Pajusalu
00385932
0000339541
see paper; ...
Simpson-Golabi-Behmel syndrome
SGBS1
Familial, X-linked recessive
-
-
-
-
Johan den Dunnen
00109422
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