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Phenotypes for disease #00171 (IBDD (isobutyryl-CoA dehydrogenase deficiency (IBDD)), OMIM:611283)
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
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
Diagnosis/Definite
: phenotype individual after molecular testing (OMIM abbreviation)
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
Phenotype details
: additional information on the phenotype of the individual, preferably use HPO terms only (http://www.human-phenotype-ontology.org/)
Protein
: result from protein staining
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
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'
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.
25 entries on 1 page. Showing entries 1 - 25.
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Legend
How to query
Phenotype ID
Diagnosis/Initial
Inheritance
Age/Examination
Diagnosis/Definite
Age/Onset
Phenotype/Onset
Phenotype details
Protein
Age/Diagnosis
Owner
Individual ID
0000000873
-
Familial
-
-
-
-
no clinical phenotype at age of diagnosis
-
00y03m
Division of Human Genetics, Innsbruck
00001719
0000000874
-
Unknown
-
-
-
-
ascertainment unknown
-
-
Division of Human Genetics, Innsbruck
00001720
0000000875
-
Familial
-
-
-
-
ascertainment clinical presentation
-
-
Division of Human Genetics, Innsbruck
00001721
0000000876
-
Familial
-
-
-
-
ascertainment clinical presentation
-
-
Division of Human Genetics, Innsbruck
00001722
0000000877
-
Unknown
-
-
-
-
ascertainment clinical presentation
-
-
Division of Human Genetics, Innsbruck
00001723
0000000878
-
Unknown
-
-
-
-
ascertainment newborn screening
-
-
Division of Human Genetics, Innsbruck
00001724
0000000879
-
Unknown
-
-
-
-
ascertainment newborn screening
-
-
Division of Human Genetics, Innsbruck
00001725
0000000880
-
Unknown
-
-
-
-
ascertainment newborn screening
-
-
Division of Human Genetics, Innsbruck
00001726
0000000881
-
Unknown
-
-
-
-
ascertainment newborn screening
-
-
Division of Human Genetics, Innsbruck
00001727
0000000882
-
Unknown
-
-
-
-
ascertainment clinical presentation
-
2y
Division of Human Genetics, Innsbruck
00001728
0000000883
-
Unknown
-
-
-
-
ascertainment newborn screening
-
00y00m18d
Division of Human Genetics, Innsbruck
00001729
0000000884
-
Unknown
-
-
-
-
ascertainment unknown
-
-
Division of Human Genetics, Innsbruck
00001730
0000000885
-
Unknown
-
-
-
-
ascertainment unknown
-
-
Division of Human Genetics, Innsbruck
00001731
0000000886
-
Unknown
-
-
-
-
ascertainment newborn screening
-
00y00m09d
Division of Human Genetics, Innsbruck
00001732
0000000887
-
Unknown
-
-
-
-
-
-
00y03m
Division of Human Genetics, Innsbruck
00001733
0000000888
-
Unknown
-
-
-
-
ascertainment newborn screening
-
00y00m05d
Division of Human Genetics, Innsbruck
00001734
0000000889
-
Unknown
-
-
-
-
ascertainment newborn screening
-
00y00m14d
Division of Human Genetics, Innsbruck
00001735
0000000890
-
Unknown
-
-
-
-
ascertainment newborn screening
-
00y00m16d
Division of Human Genetics, Innsbruck
00001736
0000000891
-
Unknown
-
-
-
-
ascertainment newborn screening
-
00y00m07d
Division of Human Genetics, Innsbruck
00001737
0000000892
-
Unknown
-
-
-
-
ascertainment newborn screening
-
00y00m42d
Division of Human Genetics, Innsbruck
00001738
0000000893
-
Unknown
-
-
-
-
ascertainment newborn screening
-
00y02m
Division of Human Genetics, Innsbruck
00001739
0000000894
-
Unknown
-
-
-
-
ascertainment newborn screening
-
00y00m21d
Division of Human Genetics, Innsbruck
00001740
0000000895
-
Familial
-
-
-
-
ascertainment newborn screening; additionally affected with glutaric aciduria type 1
-
00y00m01d
Division of Human Genetics, Innsbruck
00001741
0000000896
-
Unknown
-
-
-
-
ascertainment newborn screening
-
00y00m09d
Division of Human Genetics, Innsbruck
00001742
0000143265
-
Familial, autosomal recessive
-
-
-
-
-
-
-
Belen Perez
00181001
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