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Phenotypes for disease #01575 (HHT (telangiectasia hemorrhagic, hereditary (HHT)))
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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^p.(Arg
all entries beginning with 'p.(Arg'
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Date
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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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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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 'South Asian', but not containing 'South East Asian'
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71 entries on 1 page. Showing entries 1 - 71.
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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
0000053401
hereditary hemorrhagic telangiectasia with frequent epistaxis at 12y
-
-
Unknown
-
-
-
-
-
Sophie Nambot
00038520
0000053403
hereditary hemorrhagic telangiectasia with recurrent but sporadic epistaxis
-
-
Unknown
-
-
-
-
-
Sophie Nambot
00038516
0000078715
-
-
-
Unknown
-
-
-
-
-
Gemeinschaftspraxis für Humangenetik Dresden
00100507
0000078717
suspected Morbus Osler
-
-
Familial, autosomal dominant
-
-
-
-
-
Andreas Laner
00035680
0000078718
suspected Morbus Osler with epistaxis (also familiar), intracranial haemorrhage with 4 arteriovenous malformations
-
-
Familial, autosomal dominant
-
-
-
-
-
Andreas Laner
00035681
0000078719
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Andreas Laner
00035682
0000078720
suspected Morbus Osler
-
-
Familial, autosomal dominant
-
-
-
-
-
Andreas Laner
00035683
0000078721
clinical Morbus Osler
-
-
Familial, autosomal dominant
-
-
-
-
-
Andreas Laner
00035687
0000078722
suspected Morbus Osler
-
-
Familial, autosomal dominant
-
-
-
-
-
Andreas Laner
00035685
0000078723
suspected Morbus Osler with epistaxis (also familiar), intracranial haemorrhage with 4 arteriovenous malformations
-
-
Familial, autosomal dominant
-
-
-
-
-
Andreas Laner
00035684
0000078724
suspected Morbus Osler
-
-
Familial, autosomal dominant
-
-
-
-
-
Andreas Laner
00035689
0000155273
epistaxis, pulmonary arteriovenous malformation, hepatic arteriovenous malformation
hereditary haemorrhagict elangiectasia
HHT-2
Familial, autosomal dominant
63y
-
-
-
-
Johan den Dunnen
00207450
0000155280
epistaxis, telangiectasia, pulmonary arteriovenous malformation
hereditary haemorrhagict elangiectasia
HHT-2
Familial, autosomal dominant
27y
-
-
-
-
Johan den Dunnen
00207502
0000155281
epistaxis, telangiectasia, pulmonary arteriovenous malformation
hereditary haemorrhagict elangiectasia
HHT-2
Unknown
41y
-
-
-
-
Johan den Dunnen
00207503
0000155282
epistaxis, telangiectasia, colon arteriovenous malformation
hereditary haemorrhagict elangiectasia
HHT-2
Familial, autosomal dominant
64y
-
-
-
-
Johan den Dunnen
00207504
0000155283
epistaxis, telangiectasia, pulmonary arteriovenous malformation, hepatic arteriovenous malformation
hereditary haemorrhagict elangiectasia
HHT-2
Familial, autosomal dominant
47y
-
-
-
-
Johan den Dunnen
00207505
0000155284
telangiectasia, pulmonary arteriovenous malformation, hepatic arteriovenous malformation
hereditary haemorrhagict elangiectasia
HHT-2
Familial, autosomal dominant
70y
-
-
-
-
Johan den Dunnen
00207506
0000155285
epistaxis, diffuse arteriovenous malformation
hereditary haemorrhagict elangiectasia
HHT-2
Familial, autosomal dominant
49y
-
-
-
-
Johan den Dunnen
00207507
0000155286
epistaxis, telangiectasia, pulmonary arteriovenous malformation
hereditary haemorrhagict elangiectasia
HHT-2
Familial, autosomal dominant
80y
-
-
-
-
Johan den Dunnen
00207508
0000167202
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218666
0000167203
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218667
0000167206
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218670
0000167207
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218671
0000167208
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218672
0000167218
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218682
0000167219
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218683
0000167238
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218702
0000167239
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218703
0000167240
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218704
0000167241
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218705
0000167242
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218706
0000167258
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218722
0000167266
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218730
0000167267
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218731
0000167270
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218734
0000167311
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218775
0000167312
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218776
0000167314
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218778
0000167318
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218782
0000167346
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218810
0000167347
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218811
0000167349
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218813
0000167350
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218814
0000167357
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218821
0000167358
HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218822
0000167359
HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218823
0000167360
HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218824
0000167379
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218843
0000167380
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218844
0000167381
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218845
0000167382
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218846
0000167383
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218847
0000167385
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218849
0000167386
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218850
0000167387
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218851
0000167440
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218904
0000167441
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218905
0000167442
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218906
0000167443
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218907
0000167444
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218908
0000167445
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218909
0000167446
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218910
0000167447
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218911
0000207614
57y-deceased; recurrent epistaxis, telangiectasia; family history
telangiectasia
HHT-1
Familial, autosomal dominant
57y
-
-
-
-
Johan den Dunnen
00269823
0000207615
recurrent epistaxis, telangiectasia, visceral arteriovenous malformation, liver arteriovenous malformation, chronic HHT-related GI bleeding; family history
telangiectasia
HHT-2
Familial, autosomal dominant
70y
-
-
-
-
Johan den Dunnen
00269824
0000207616
recurrent epistaxis, telangiectasia, visceral arteriovenous malformation, liver arteriovenous malformation, chronic HHT-related GI bleeding; family history
telangiectasia
HHT-2
Familial, autosomal dominant
66y
-
-
-
-
Johan den Dunnen
00269825
0000207617
recurrent epistaxis, telangiectasia; family history
telangiectasia
HHT-2
Familial, autosomal dominant
71y
-
-
-
-
Johan den Dunnen
00269826
0000207618
recurrent epistaxis, telangiectasia, visceral arteriovenous malformation, liver arteriovenous malformation, chronic HHT-related GI bleeding; family history
telangiectasia
HHT-2
Familial, autosomal dominant
68y
-
-
-
-
Johan den Dunnen
00269827
0000330504
see paper; ..., classical hereditary hemorrhagic telangiectasia, severe nosebleeds needing blood transfusion and intravenous iron
hereditary hemorrhagic telangiectasia
-
Unknown
-
-
-
-
-
Johan den Dunnen
00440592
0000330505
see paper; ..., classical hereditary hemorrhagic telangiectasia, daily nosebleeds; one had pulmonary arteriovenous malformations requiring treatment, hemihypertrophy (left-right axis defect)
hereditary hemorrhagic telangiectasia
-
Unknown
-
-
-
-
-
Johan den Dunnen
00440593
0000330506
see paper; ..., colonic and gastric polyposis, nosebleeds, mucocutaneous telangiectasia, pulmonary AVMs treated by embolization; JPHT family history
hereditary hemorrhagic telangiectasia
JPHT
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00440594
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