Global Variome shared LOVD
PIGT (phosphatidylinositol glycan anchor biosynthes...)
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Curator:
Philippe Campeau
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Phenotypes for disease #00183 (DEE7 (encephalopathy, developmental and epileptic, type 7), OMIM:613720)
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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Text
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all entries not containing 'fs'
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Text
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all entries beginning with 'p.(Arg'
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Text
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all entries ending with 'Ser)'
=""
Text
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Text
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combination
Text
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Date
2020
all entries matching the year 2020
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Date
2020-03|2020-04
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 after June, 2020
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Date
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all entries on or after June 15th, 2020
combination
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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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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19 entries on 1 page. Showing entries 1 - 19.
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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
0000041475
-
-
-
Unknown
-
-
-
-
-
NeuroMeGen
00054788
0000041476
-
-
-
Unknown
-
-
-
-
-
NeuroMeGen
00054821
0000041477
-
-
-
Unknown
-
-
-
-
-
NeuroMeGen
00054822
0000041478
-
-
-
Unknown
-
-
-
-
-
NeuroMeGen
00054823
0000041479
-
-
-
Unknown
-
-
-
-
-
NeuroMeGen
00054824
0000041480
-
-
-
Unknown
-
-
-
-
-
NeuroMeGen
00054825
0000041481
-
-
-
Unknown
-
-
-
-
-
NeuroMeGen
00054826
0000041482
-
-
-
Unknown
-
-
-
-
-
NeuroMeGen
00054827
0000041483
-
-
-
Unknown
-
-
-
-
-
NeuroMeGen
00054828
0000041484
-
-
-
Unknown
-
-
-
-
-
NeuroMeGen
00054829
0000060406
Epileptic encephalopathy, early infantile, 7 (OMIM:613720)
-
-
Isolated (sporadic)
-
-
-
-
-
Daniel Trujillano
00080837
0000070607
profound IDD, epileptic encephalopathy, hypotonia, dysautonomia, microcephaly; CSF GABA free 0.007 umol/L (reference range: 0.017- 0.067) CSF GABA total 4.300 umol/L (reference range: 4.2-13.4) low CSF GABA, mitochondrial complex I and II deficiency
-
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00092271
0000087491
Developmental delay, hypotonia, seizures during first year of life
-
-
Isolated (sporadic)
-
-
-
-
-
Bernt Popp
00111406
0000257304
Developmental delay, seizures, hypotonia, microcephaly
-
-
Familial, autosomal dominant
-
-
-
-
-
Anju Shukla
00361907
0000257617
Epileptic encephalopathy with neonatal seizures from day 1, suspected Otahara syndrome, severe combined developmental delay, marked muscular hypotonia
0y
-
Unknown
-
-
-
-
-
Andreas Laner
00362203
0000272296
Autism, Autistic behavior, Seizure, Global developmental delay, Abnormal nervous system physiology, Neurodevelopmental delay
-
5y
Unknown
-
-
-
-
-
Andreas Laner
00377115
0000296423
Behavioral abnormality, Stereotypy, Hypotonia, Delayed speech and language development, Global developmental delay, Poor fine motor coordination
-
-
Unknown
07y
-
-
-
-
Andreas Laner
00403727
0000323533
Seizure, Motor delay, Infantile onset
-
-
Unknown
00y04m
-
-
-
-
Andreas Laner
00432970
0000350382
-
-
-
Unknown
-
-
-
-
-
Min Peng
00464343
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