Global Variome shared LOVD
ALG9 (asparagine-linked glycosylation 9, alpha-1,2-...)
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Curator:
Gert Matthijs
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Phenotypes for disease #05374 (MTDPS (mitochondrial DNA depletion syndrome (MTDPS)))
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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all entries containing 'Arg'
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Text
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all entries not containing 'fs'
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Text
^p.(Arg
all entries beginning with 'p.(Arg'
$
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all entries ending with 'Ser)'
=""
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combination
Text
*|Ter !fs
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Date
2020
all entries matching the year 2020
|
Date
2020-03|2020-04
all entries matching March or April, 2020
!
Date
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all entries not matching March, 2020
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Date
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all entries before the year 2020
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Date
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all entries in or before June, 2020
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Date
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all entries after June, 2020
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Date
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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
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Numeric
<=23
all entries lower than, or equal to, 23
>
Numeric
>23
all entries higher than 23
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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'
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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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36 entries on 1 page. Showing entries 1 - 36.
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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
0000119805
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147089
0000119806
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147090
0000119807
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147091
0000119808
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147092
0000119809
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147093
0000119810
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147094
0000119811
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147095
0000119812
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147096
0000119813
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147097
0000119814
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147098
0000119815
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147099
0000119816
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147100
0000119817
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147101
0000119818
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147102
0000119819
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147103
0000119820
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147104
0000119821
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147105
0000119822
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147106
0000119823
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147107
0000119824
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147108
0000119825
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147109
0000119826
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147110
0000119827
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147111
0000119828
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147112
0000119829
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147113
0000119830
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147114
0000119831
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147115
0000119832
-
-
see paper; …
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00147116
0000125979
distal myopathy
-
see paper; …
Familial, autosomal recessive
-
27y
-
-
Johan den Dunnen
00153298
0000125980
distal myopathy
-
see paper; …
Familial, autosomal recessive
-
22y
-
-
Johan den Dunnen
00153299
0000125981
distal myopathy
-
see paper; …
Familial, autosomal recessive
-
26y
-
-
Johan den Dunnen
00153300
0000233161
mitochondrial DNA depletion syndromes
-
characteristic phenotype (Neonatal cholestasis, failure to thrive, metabolic acidosis)
Familial, autosomal recessive
3m
-
-
-
Johan den Dunnen
00307447
0000233170
mitochondrial DNA depletion syndromes
-
intestinal failure ass. liver disease, mild retardation
Unknown
1y
-
-
-
Johan den Dunnen
00307456
0000233171
mitochondrial DNA depletion syndromes
-
liver cirrhosis, celiac disease, mass. increased alpha‐feto protein
Unknown
5y
-
-
-
Johan den Dunnen
00307457
0000233172
mitochondrial DNA depletion syndromes
-
liver fibrosis with portal hypertension
Unknown
17y
-
-
-
Johan den Dunnen
00307458
0000292917
progressive dystonic features
MTDPS17
tip-toe walking, high frequency tremors, severe early-onset generalized dystonia
Familial, autosomal recessive
-
-
-
-
Anum Shafique
00399377
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