Global Variome shared LOVD
FGF14 (fibroblast growth factor 14)
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Phenotypes for disease #04204 (ASD (septal defect, atrial (ASD)))
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
How to query this table
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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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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
<=2020-06
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
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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
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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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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.
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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93 entries on 1 page. Showing entries 1 - 93.
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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
0000025880
-
-
-
Isolated (sporadic)
12y
-
-
-
-
Johan den Dunnen
00032403
0000025881
no malformations eyes/teeth/umbilicus
-
-
Isolated (sporadic)
03y
-
-
-
-
Johan den Dunnen
00032404
0000082847
autism spectrum disorder
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00104965
0000204383
JLNS: jervell and lange-nielsen syndrome
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266674
0000204386
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266676
0000204387
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266677
0000204388
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266678
0000204395
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266679
0000204402
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266682
0000204409
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266685
0000204429
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266693
0000204436
pulmonary atresia with ventricular septal defect
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266695
0000204446
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266712
0000204451
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266714
0000204459
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266718
0000204468
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266720
0000204473
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266721
0000204480
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266724
0000204495
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266731
0000204507
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266737
0000204514
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266738
0000204524
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266741
0000204534
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266744
0000204544
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266747
0000204595
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266778
0000204620
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266788
0000204647
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266814
0000204655
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266825
0000204657
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266827
0000204667
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266830
0000204680
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266839
0000204689
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266845
0000204702
JLNS: jervell and lange-nielsen syndrome
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266851
0000204704
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266852
0000204711
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266855
0000204715
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266858
0000204719
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266862
0000204723
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266865
0000204726
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266866
0000204741
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266880
0000204746
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266887
0000204748
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266888
0000204751
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266891
0000204755
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266893
0000204757
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266894
0000204760
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266895
0000204766
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266902
0000204775
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266909
0000204779
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266911
0000204783
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266913
0000204787
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266915
0000204790
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266916
0000204805
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266927
0000204810
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266929
0000204812
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266930
0000204815
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266932
0000204819
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266934
0000204821
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266935
0000204824
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266936
0000204830
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266941
0000204841
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266948
0000204848
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266953
0000204870
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266963
0000204879
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266966
0000204881
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266967
0000204882
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266968
0000204883
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266969
0000204885
JLNS: jervell and lange-nielsen syndrome
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266972
0000204887
JLNS: jervell and lange-nielsen syndrome
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266973
0000204890
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266974
0000204895
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266975
0000204903
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266977
0000204907
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00266981
0000204935
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00001464
0000204936
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00001471
0000204940
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00001480
0000204942
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00001482
0000204943
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00001483
0000204945
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00267012
0000204950
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00267014
0000204951
-
-
-
Unknown
-
-
-
-
-
Liliana Dain
00267015
0000227567
Atrial Septal Aneurysm, Mitral Valve Prolaps
-
-
Familial, autosomal dominant
-
-
-
-
-
Patrice Bouvagnet
00300269
0000227568
Atrial Septal Defect, Mitral Valve Prolaps
-
-
Familial, autosomal dominant
-
-
-
-
-
Patrice Bouvagnet
00300270
0000238717
pulmonary arterial hypertension (HP:0002092)
pulmonary arterial hypertension/PAH
-
Familial, autosomal dominant
-
-
-
-
-
Yi-Qing Yang
00314958
0000279678
syndromic ASD
-
-
Isolated (sporadic)
-
-
-
-
-
Alaaeldin Fayez
00385875
0000281255
see paper; ..., secundum atrial septal defect (HP:0001684)
atrial septal defect
ASD7
Familial, autosomal dominant
30y
30y
-
Atrial septal defect (HP:0001631)
-
Alaaeldin Fayez
00387689
0000281260
Atrioventricular block (HP:0001678), Mildly reduced ejection fraction (HP:0012663), Apical hypertrabeculation of the left ventricle (HP:0031195), Left ventricular noncompaction cardiomyopathy (HP:0011664), Paroxysmal atrial fibrillation (HP:0004757), Ventricular tachycardia (HP:0004756), Perimembranous ventricular septal defect (HP:0011682), Atrial septal defect (HP:0001631), Persistent left superior vena cava (HP:0005301), Absent right superior vena cava (HP:0011666), First degree atrioventricular block (HP:0011705), Third degree atrioventricular block (HP:0001709),
-
-
Familial, autosomal dominant
-
-
-
-
-
Alaaeldin Fayez
00387692
0000288600
Down syndrome, congenital heart defect; unaffected carrier father
congenital heart defect
-
Unknown
-
-
-
-
-
Johan den Dunnen
00204350
0000335932
see paper; ..., atrial septal defect corrected surgically in early childhood, normal left ventricular function
atrial septal defect
ASD4
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00446730
0000335933
see paper; ..., small atrial septal defect, mild coarctation aorta; 6m/6y-mild-to-moderate pulmonary hypertension; 31y-percutaneous device closure ASD; ECG reduced LV function
atrial septal defect
ASD4
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00446731
0000335934
see paper; ..., 7m-atrial septal defect
atrial septal defect
ASD4
Familial, autosomal dominant
00y07m
-
-
-
-
Johan den Dunnen
00446732
0000335935
see paper; ..., congenital atrial septal defects, patent foramen ovale, cardiac valve defects
atrial septal defect
ASD4
Familial, autosomal dominant
16y
-
-
-
-
Johan den Dunnen
00446733
0000335936
see paper; ..., adult‑onset dilated cardiomyopathy; family congenital atrial septal defect
atrial septal defect
ASD4
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00446734
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