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Phenotypes for disease #04203 (ATFB (fibrillation, atrial (ATFB)))
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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!fs
all entries not containing 'fs'
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Text
^p.(Arg
all entries beginning with 'p.(Arg'
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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
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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
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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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Numeric
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all entries higher than, or equal to, 23
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Numeric
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all entries with values from 20 to 29, but not equal to 23
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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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59 entries on 1 page. Showing entries 1 - 59.
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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
0000025879
lone atrial fibrillation, no malformations eyes/teeth/umbilicus/heart; onset 32y
-
-
Isolated (sporadic)
46y
-
-
-
-
Johan den Dunnen
00032402
0000025884
see paper; ..
-
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00032407
0000129559
The proband had a sudden death subsequently resuscitated; frequent arrythmias were reported
Epilepsy? Brugada Syndrome?
SUDEP
Familial
38y
35y
-
Epilepsy? Brugada?
-
Nicola Marziliano
00164519
0000129911
-
-
-
Isolated (sporadic)
-
-
-
-
-
Florence van Tienen
00165023
0000171680
-
atrial fibrillation
ATFB-11
Familial, autosomal dominant
-
-
-
-
-
Yi-Qing Yang
00226567
0000171681
-
atrial fibrillation
ATFB-11
Familial, autosomal dominant
-
-
-
-
-
Yi-Qing Yang
00226568
0000171682
-
atrial fibrillation
ATFB-11
Familial
-
-
-
-
-
Johan den Dunnen
00226569
0000171683
-
atrial fibrillation
ATFB-11
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00226570
0000171684
-
atrial fibrillation
ATFB-11
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00226571
0000171685
-
atrial fibrillation
ATFB-11
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00226572
0000171686
-
atrial fibrillation
ATFB-11
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00226573
0000171687
-
atrial fibrillation, idiopathic
ATFB-11
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00226574
0000171688
-
atrial fibrillation, idiopathic
ATFB-11
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00226575
0000171689
-
atrial fibrillation, idiopathic
ATFB-11
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00226576
0000171698
-
atrial fibrilation, associted with
-
Familial
-
-
-
-
-
Johan den Dunnen
00226585
0000174738
-
-
-
Unknown
-
-
56y
-
-
Sandra Hoffmann
00234319
0000174749
-
-
-
Unknown
-
-
51y
-
-
Sandra Hoffmann
00234318
0000174751
-
-
-
Unknown
-
-
-
-
-
Sandra Hoffmann
00234331
0000174752
-
-
-
Unknown
-
-
52y
-
-
Sandra Hoffmann
00234332
0000174756
-
-
-
Unknown
-
-
60y
-
-
Sandra Hoffmann
00234336
0000174757
-
-
-
Unknown
-
-
72y
-
-
Sandra Hoffmann
00234337
0000174763
atrial fibrillation (permanent 2x, persistent 1x, paroxysmal 1x); ECG heart rate 62-87 beats/min, QRS interval 96-116 ms, corrected QT interval 435-528; ECG left atrial diameter 30-38mm, left ventricular ejection fraction 60-65%
atrial fibrillation
-
Familial, autosomal dominant
20y-53y
20y-43y
-
-
-
Johan den Dunnen
00234344
0000204422
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266689
0000204503
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266734
0000204521
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266739
0000204541
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266745
0000204556
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266756
0000204569
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266764
0000204583
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266772
0000204607
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266781
0000204665
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266829
0000204699
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266846
0000204847
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266951
0000204911
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266984
0000204914
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266986
0000204915
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266988
0000204921
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266997
0000204922
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266999
0000204924
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00267001
0000218010
-
Atrial fibrillation, susceptibility to
-
Unknown
-
-
-
-
-
Julia Lopez
00284269
0000218011
-
Atrial fibrillation
-
Unknown
-
-
-
-
-
Julia Lopez
00284319
0000218012
-
Atrial fibrillation
-
Unknown
-
-
-
-
-
Julia Lopez
00284320
0000218013
-
Atrial fibrillation
-
Unknown
-
-
-
-
-
Julia Lopez
00284325
0000218014
-
Atrial fibrillation
-
Unknown
-
-
-
-
-
Julia Lopez
00284415
0000218015
-
Atrial fibrillation and bradycardia
-
Unknown
-
-
-
-
-
Julia Lopez
00284439
0000218016
-
Atrial fibrillation, lone, early-onset
-
Unknown
-
-
-
-
-
Julia Lopez
00284872
0000218017
-
Atrial fibrillation, early-onset
-
Unknown
-
-
-
-
-
Julia Lopez
00285407
0000218018
-
Atrial fibrillation, early-onset
-
Unknown
-
-
-
-
-
Julia Lopez
00285425
0000233127
see paper; ..., atrial fibrillation
atrial fibrillation
-
Unknown
-
-
-
-
-
Johan den Dunnen
00307333
0000324257
see paper; ..., early onset atrial fibrillation
atrial fibrillation
ATFB
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00433879
0000340342
-
-
-
Unknown
-
<60y
-
-
-
Sandra Hoffmann
00451683
0000340344
-
-
-
Unknown
-
<60y
-
-
-
Sandra Hoffmann
00451685
0000340348
-
-
-
Unknown
-
-
<60y
-
-
Sandra Hoffmann
00451688
0000340349
-
-
-
Unknown
-
-
<60y
-
-
Sandra Hoffmann
00451689
0000340350
-
-
-
Unknown
-
<60y
-
-
-
Sandra Hoffmann
00451690
0000340351
-
-
-
Unknown
-
<60y
-
-
-
Sandra Hoffmann
00451691
0000340352
-
-
-
Unknown
-
<60y
-
-
-
Sandra Hoffmann
00451692
0000340353
-
-
-
Unknown
-
<60y
-
-
-
Sandra Hoffmann
00451693
0000341637
Dental developmental abnormalities and hypoplastic fifth distal phalanges/nails as well as mild facial dysmorphisms characterized by a bulbous nasal tip and micrognathia.
-
-
Familial, autosomal dominant
-
-
-
-
-
Yi-Qing Yang
00452991
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