Global Variome shared LOVD
ASPA (aspartoacylase)
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Curators:
Gajja Salomons
and
Eric Wever
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Phenotypes for disease #00353 (DRVT (Dravet syndrome), OMIM:607208)
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
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Date
2020
all entries matching the year 2020
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Date
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all entries matching March or April, 2020
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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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Date
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all entries on or after June 15th, 2020
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Date
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all entries in 2019 or 2020, and before March, 2020
Numeric
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all entries exactly matching 23
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Numeric
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all entries exactly matching 23 or 24
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Numeric
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all entries not exactly matching 23
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Numeric
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all entries lower than 23
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Numeric
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all entries lower than, or equal to, 23
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Numeric
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Numeric
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Numeric
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Matches
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all entries containing 'Asian', 'asian', including 'Caucasian', 'caucasian', etc.
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all entries containing 'Asian' but not containing 'Caucasian'
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all entries containing 'Asian' or 'African', but not containing 'Caucasian'
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all entries containing 'South Asian', but not containing 'South East Asian'
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31 entries on 1 page. Showing entries 1 - 31.
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Legend
How to query
Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000014934
-
-
-
Unknown
-
-
-
-
-
Lab Zuffardi
00016320
0000060431
Dravet syndrome (OMIM:607208)
-
-
Isolated (sporadic)
-
-
-
-
-
Daniel Trujillano
00080862
0000060638
Dravet syndrome (PMID:19710327)
-
-
Familial, autosomal recessive
-
-
-
-
-
Daniel Trujillano
00081069
0000124435
-
seizure susceptibility
EiEE-6
Unknown
-
-
-
-
-
Christoph Lossin
00152089
0000124436
-
Dravet syndrome
EiEE-6
Unknown
-
-
-
-
-
Christoph Lossin
00152090
0000124437
-
Dravet syndrome
EiEE-6
Unknown
-
-
-
-
-
Christoph Lossin
00152091
0000124438
-
Dravet syndrome
EiEE-6
Unknown
-
-
-
-
-
Christoph Lossin
00152092
0000124439
-
Dravet syndrome
EiEE-6
Unknown
-
-
-
-
-
Christoph Lossin
00152093
0000124440
-
SMEB-MA
EiEE-6
Unknown
-
-
-
-
-
Christoph Lossin
00152094
0000124441
-
complex febrile seizures
EiEE-6
Unknown
-
-
-
-
-
Christoph Lossin
00152095
0000124442
-
febrile seizures
EiEE-6
Unknown
-
-
-
-
-
Christoph Lossin
00152096
0000124443
-
febrile seizures, GSW, IGW
EiEE-6
Unknown
-
-
-
-
-
Christoph Lossin
00152097
0000124444
-
Dravet syndrome
EiEE-6
Unknown
-
-
-
-
-
Christoph Lossin
00152098
0000124445
-
febrile seizures
EiEE-6
Unknown
-
-
-
-
-
Christoph Lossin
00152099
0000124446
-
Dravet syndrome
EiEE-6
Unknown
-
-
-
-
-
Christoph Lossin
00152100
0000124447
-
Dravet syndrome
EiEE-6
Unknown
-
-
-
-
-
Christoph Lossin
00152101
0000124448
-
febrile seizures, IGE
EiEE-6
Unknown
-
-
-
-
-
Christoph Lossin
00152102
0000124449
-
SMEB-MA
EiEE-6
Unknown
-
-
-
-
-
Christoph Lossin
00152103
0000159275
see paper; …
Dravet syndrome
EIEE-6
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00210710
0000159276
see paper; …
Dravet syndrome
EIEE-6
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00210711
0000159277
see paper; …
febrile seizures plu
EIEE-6
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00210712
0000159278
see paper; …
Dravet syndrome
EIEE-6
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00210713
0000159279
see paper; …
Dravet syndrome
EIEE-6
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00210714
0000159280
see paper; …
Dravet syndrome
EIEE-6
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00210715
0000159281
see paper; …
Dravet syndrome
EIEE-6
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00210716
0000241754
Febrile seizure (within the age range of 3 months to 6 years); Generalized-onset seizure
-
-
Unknown
05y
-
-
-
-
Andreas Laner
00317970
0000281845
see paper; ...
-
DRVT
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00388292
0000281846
see paper; ...
-
DRVT
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00388293
0000281847
see paper; ...
-
DRVT
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00388294
0000346979
Seizure, Febrile seizure outside the age of 3 months to 6 years, Neurodevelopmental delay, Motor delay, Delayed speech and language development, Hypotonia, Abnormal brain morphology, Poor gross motor coordination, Sleep abnormality
-
-
Isolated (sporadic)
07y
-
-
-
-
Andreas Laner
00458547
0000351362
HPO: Seizure; Seizures since the 7th month of life, a variety of medications tried, no seizure relief achieved
-
-
Isolated (sporadic)
01y
-
-
-
-
Andreas Laner
00465969
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