Global Variome shared LOVD
QDPR (quinoid dihydropteridine reductase)
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Phenotypes for disease #01834 (F12D (deficiency, factor XII), OMIM:234000)
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 beginning with 'p.(Arg'
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Date
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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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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 'South Asian', but not containing 'South East Asian'
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56 entries on 1 page. Showing entries 1 - 56.
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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
0000130188
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165323
0000130189
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165324
0000130190
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165325
0000130191
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165326
0000130192
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165327
0000130196
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165331
0000130197
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165332
0000130198
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165333
0000130199
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165334
0000130200
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165335
0000130201
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165336
0000130202
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165337
0000130203
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165338
0000130204
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165339
0000130205
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165340
0000130206
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165341
0000130207
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165342
0000130208
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165343
0000130209
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165344
0000130212
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165347
0000130213
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165348
0000130214
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165349
0000130215
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165350
0000130218
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165353
0000130219
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165354
0000130220
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165355
0000130221
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165356
0000130222
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165357
0000130223
-
factor XII deficiency
-
Unknown
-
-
-
-
-
Johan den Dunnen
00165358
0000280342
Thrombotic complications and heart infarction
-
-
Familial
-
-
-
-
-
Christian Drouet
00386542
0000281502
-
-
-
Unknown
-
-
-
-
-
Christian Drouet
00387933
0000318701
Prolonged aPTT, persistently undetectable FXII function and normal PT: detected for tooth extractions, laparoscopic cholecystectomy, breast tumor excision, extracorporeal shockwave lithotomy
-
F12D
Familial, autosomal recessive
-
-
-
-
-
Christian Drouet
00427687
0000318702
Proband without any bleeding disorder; prolonged aPTT detected in a patient with a prostatectomy
-
F12D
Familial, autosomal recessive
-
71y
-
-
-
Christian Drouet
00427688
0000318703
Proband presenting with thrombus in the inferior vena cava and common iliac as shown by lower limb venography.
-
-
Familial
27y
-
-
-
-
Christian Drouet
00427689
0000318704
Proband without any bleeding disorder; prolonged aPTT discovered in a patient for a liver biopsy
-
F12D
Familial, autosomal recessive
-
55y
-
-
-
Christian Drouet
00427690
0000318755
Prolonged aPTT, persistently undetectable FXII function, normal PT: detected for tooth extractions, laparoscopic cholecystectomy, breast tumor excision, extracorporeal shockwave lithotomy
-
F12D
Familial, autosomal recessive
-
-
-
-
-
Christian Drouet
00427779
0000318756
Prolonged aPTT, persistently undetectable FXII function and normal PT: tooth extractions, laparoscopic cholecystectomy, breast tumor excision, extracorporeal shockwave lithotomy
-
F12D
Familial, autosomal recessive
-
48y
-
-
-
Christian Drouet
00427780
0000321100
Proband presenting with mild haemorrhagic manifestations
-
-
Familial
-
-
-
-
-
Christian Drouet
00430292
0000321101
Proband presenting with mild haemorrhagic manifestations
-
-
Familial
-
-
-
-
-
Christian Drouet
00430293
0000321102
Proband presenting with haemorrhagic manifestations
-
-
Familial
-
-
-
-
-
Christian Drouet
00430294
0000321113
Homozygous proband presenting with haemorrhage complications
-
21y
Familial
-
-
-
-
-
Christian Drouet
00430299
0000321115
Homozygous proband presenting with haemorrhage complications
-
60y
Familial
-
-
-
-
-
Christian Drouet
00430302
0000321894
Homozygous proband presenting with a prolonged aPTT
-
-
Familial
-
58y
-
-
-
Christian Drouet
00431294
0000326603
Homozygous proband presenting with significantly prolonged activated partial thromboplastin time (APTT), an extremely reduced FXII activity (FXII:C) and antigenic FXII (FXII:Ag).
-
-
Familial, autosomal recessive
-
51y
-
-
-
Christian Drouet
00436424
0000326668
A compound heterozygote proband presenting with a prolonged aPPT; congenital heart anomaly
-
-
Familial
-
04y
-
-
-
Christian Drouet
00436490
0000326669
A homozygous proband presenting with a prolonged aPTT; anal fistula
-
-
Familial
-
50y
-
-
-
Christian Drouet
00436491
0000326670
A compound heterozygous proband presenting with a prolonged aPTT; pituitary macroadenoma
-
-
Familial
-
53y
-
-
-
Christian Drouet
00436492
0000332876
Proband presenting with a prolonged aPTT
-
-
Familial
-
-
-
-
-
Christian Drouet
00443560
0000333635
Proband presenting with a prolonged aPTT
-
-
Familial
-
68y
-
-
-
Christian Drouet
00444382
0000333636
Proband presenting with a prolonged aPTT
-
-
Familial
-
52y
-
-
-
Christian Drouet
00444383
0000333637
Proband presenting with a prolonged aPTT
-
-
Familial
-
43y
-
-
-
Christian Drouet
00444384
0000333639
Proband presenting with a prolonged aPTT
-
-
Familial
-
-
-
-
-
Christian Drouet
00444386
0000340668
Proband presenting with a significantly prolonged aPTT; no history of bleeding episodes during the previous deliveries nor any tooth extractions
-
-
Familial, autosomal recessive
36y
-
-
-
-
Christian Drouet
00452064
0000349735
Proband presenting with Hageman trait and prolonged aPTT
-
-
Familial
-
-
-
-
-
Christian Drouet
00462235
0000352759
Proband presenting with a significantly prolonged APTT (180.0 s) and a decreased FⅫ:C and FⅫ:Ag levels (<1%)
-
-
Familial
-
47y
-
-
-
Christian Drouet
00467549
0000352762
Proband presenting with a prolonged aPTT
-
-
Familial
-
-
-
-
-
Christian Drouet
00467555
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