Global Variome shared LOVD
LRRFIP1 (leucine rich repeat (in FLII) interacting ...)
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Phenotypes for disease #00264 (DEE1 (encephalopathy, developmental and epileptic, type 1), OMIM:308350)
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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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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Date
2020
all entries matching the year 2020
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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
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all entries exactly matching 23
|
Numeric
23|24
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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all entries higher than 23
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Numeric
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all entries higher than, or equal to, 23
combination
Numeric
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all entries with values from 20 to 29, but not equal to 23
Some more advanced examples:
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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'
"South Asian"
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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How to query
Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000002014
mental retardation, epilepsy
-
-
Familial, X-linked recessive
-
-
-
-
-
Johan den Dunnen
00003174
0000014896
infantile spasms, ECG-hypsarrhythmia, mental retardation, epilepsy
-
-
Familial, X-linked recessive
-
-
-
-
-
Johan den Dunnen
00003175
0000171800
initial diagnosis atypical West syndrome
early-onset epileptic encephalopathy
-
-
-
-
-
-
-
LOVD
00227778
0000171801
slight psychomotor development with eye contact, no head control
early-onset epileptic encephalopathy
-
Unknown
-
-
-
-
-
LOVD
00227779
0000171802
severe MR, nail dysplasia, sterotypes, No walking, tremor
Infantile epileptic encephalopathy
-
-
-
-
5m
-
-
LOVD
00227780
0000171803
-
early-onset epileptic encephalopathy
-
-
-
-
-
-
-
LOVD
00227781
0000171804
-
early-onset epileptic encephalopathy
-
-
-
-
-
-
-
LOVD
00227782
0000171806
-
early-onset epileptic encephalopathy
-
-
-
-
-
-
-
LOVD
00227784
0000171807
-
early-onset epileptic encephalopathy
-
-
-
-
-
-
-
LOVD
00227785
0000171808
-
early-onset epileptic encephalopathy
-
Isolated (sporadic)
-
-
-
-
-
LOVD
00227786
0000171809
evolution to West syndrome
early-onset epileptic encephalopathy
-
-
-
-
-
-
-
LOVD
00227787
0000171811
evolution to West syndrome
early-onset epileptic encephalopathy
-
-
-
-
-
-
-
LOVD
00227789
0000171812
evolution to West syndrome
early-onset epileptic encephalopathy
-
-
-
-
-
-
-
LOVD
00227790
0000171813
-
West syndrome
-
-
-
-
-
-
-
LOVD
00227791
0000171815
suppression-burst; evolution to West syndrome; no head control, no social contact, severe MR, spastic quadriplegia
Early infantile epileptic encephalopathy with suppression-burst
-
-
-
-
0d
-
-
LOVD
00227793
0000171816
suppression-burst; evolution to West syndrome; no head control, no social contact, severe MR, spastic quadriplegia
Early infantile epileptic encephalopathy with suppression-burst
-
-
-
-
43d
-
-
LOVD
00227794
0000171817
suppression-burst; no head control, no social contact, severe MR, spastic quadriplegia
Early infantile epileptic encephalopathy with suppression-burst
-
-
-
-
15d
-
-
LOVD
00227795
0000171818
suppression-burst; evolution to West syndrome; no head control, no social contact, severe MR, spastic quadriplegia
Early infantile epileptic encephalopathy with suppression-burst
-
-
-
-
2d
-
-
LOVD
00227796
0000171819
suppression-burst; evolution to West syndrome; no head control, no social contact, severe MR, spastic quadriplegia
Early infantile epileptic encephalopathy with suppression-burst
-
-
-
-
2m
-
-
LOVD
00227797
0000171820
suppression-burst; moderate MR, Quadriplegia; eye pursuit and smiling from 4m, head control and rolling over from 6m
Early infantile epileptic encephalopathy with suppression-burst
-
-
-
-
5d
-
-
LOVD
00227798
0000171821
suppression-burst; no head control, no social contact, severe MR, spastic quadriplegia
Early infantile epileptic encephalopathy with suppression-burst
-
-
-
-
1m
-
-
LOVD
00227799
0000171822
suppression-burst; evolution to West syndrome; no head control, smiling from 5m, severe MR, spastic quadriplegia
Early infantile epileptic encephalopathy with suppression-burst
-
-
-
-
3d
-
-
LOVD
00227800
0000171823
suppression-burst; evolution to West syndrome; no head control, no social contact, Severe MR, spastic quadriplegia
Early infantile epileptic encephalopathy with suppression-burst
-
-
-
-
14d
-
-
LOVD
00227801
0000171824
suppression-burst; hypertonic, no head control, no smile; mild rigospastic quadriplegia, profound developmental delay
Early infantile epileptic encephalopathy with suppression-burst
-
Isolated (sporadic)
-
-
37d
-
-
LOVD
00227802
0000171826
No head control, No visual attention, Hypotonia
West syndrome
-
-
-
-
6m
-
-
LOVD
00227804
0000171827
suppression-burst; Poor head control, poor visual attention, poor eye pursuit, severe hypotonia
Early infantile epileptic encephalopathy with suppression-burst
-
-
-
-
1m
-
-
LOVD
00227805
0000171830
Dyskinesia, hand stereotypes, Ataxic walking, No speech, Autistic features
Ohtahara syndrome
-
-
-
-
<1d
-
-
LOVD
00227808
0000171831
Dyskinesia, Axial hypertonia
Ohtahara syndrome
-
-
-
-
1m7d
-
-
LOVD
00227809
0000171832
Dyskinesia, No speech, Ataxic walking, sterotypic movements, Autistic features
Ohtahara syndrome
-
-
-
-
1d
-
-
LOVD
00227810
0000171833
No walk, No speech
Ohtahara syndrome
-
-
-
-
3d
-
-
LOVD
00227811
0000171834
Axial hypertonia, autistic features
Ohtahara syndrome
-
-
-
-
1d
-
-
LOVD
00227812
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