Global Variome shared LOVD
SLC35A1 (solute carrier family 35 (CMP-sialic acid...))
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Phenotypes for disease #01516 (JPHT (polyposis, juvenile/hereditary hemorrhagic telangiectasia syndrome (JPHT)), OMIM:175050)
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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37 entries on 1 page. Showing entries 1 - 37.
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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
0000167155
JPS
-
-
Unknown
-
-
-
-
-
Julia Lopez
00049944
0000167174
JPS
-
-
Unknown
-
-
-
-
-
Julia Lopez
00049970
0000167181
JPS
-
-
Unknown
-
-
-
-
-
Julia Lopez
00049983
0000167182
JP-HHT
-
-
Unknown
-
-
-
-
-
Julia Lopez
00049984
0000167183
JPS
-
-
Unknown
-
-
-
-
-
Julia Lopez
00049985
0000167184
JP-HHT
-
-
Unknown
-
-
-
-
-
Julia Lopez
00049986
0000167185
JP-HHT
-
-
Unknown
-
-
-
-
-
Julia Lopez
00049987
0000167186
JPS
-
-
Unknown
-
-
-
-
-
Julia Lopez
00049988
0000167187
JP-HHT
-
-
Unknown
-
-
-
-
-
Julia Lopez
00049989
0000167188
JP-HHT
-
-
Unknown
-
-
-
-
-
Julia Lopez
00049990
0000167189
JP-HHT
-
-
Unknown
-
-
-
-
-
Julia Lopez
00049991
0000167192
FJP
-
-
Unknown
-
-
-
-
-
Julia Lopez
00049996
0000167193
JPHT
-
-
Unknown
-
-
-
-
-
Julia Lopez
00049998
0000167309
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218773
0000167343
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218807
0000167344
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218808
0000167348
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218812
0000167352
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218816
0000167361
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218825
0000167396
JP-HHT
-
-
Unknown
-
-
-
-
-
Karl Heinimann
00218860
0000167484
see paper; ...
-
JPHT
Unknown
24y
-
-
-
-
Johan den Dunnen
00049992
0000167485
see paper; ...
-
JPHT
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00049945
0000167486
see paper; ...
-
JPHT
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00049946
0000167487
see paper; ...
-
-
Unknown
-
-
-
-
-
Johan den Dunnen
00049947
0000167488
see paper; ...
-
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00049948
0000167489
see paper; ...
-
JPHT
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00049949
0000167490
see paper; ...
-
JPHT
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00049997
0000167491
see paper; ...
-
JPHT
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00049999
0000167492
see paper; telangiectases, epistaxis, AVMs lung and gastrointestinal tract, colonic polyps discoverd during endoscopy, ...
hemorrhagic telangiectasia
JPHT
Unknown
37y
-
-
-
-
Johan den Dunnen
00049971
0000202099
-
JP-HHT
-
Unknown
6y
-
-
-
-
Benjamin Tschupp
00264253
0000202100
-
JP-HHT
-
Familial
-
-
-
-
-
Benjamin Tschupp
00264254
0000202101
-
JP-HHT
-
Familial
-
-
-
-
-
Benjamin Tschupp
00264255
0000202111
-
JP-HHT
-
Familial
7y
-
-
-
-
Benjamin Tschupp
00264265
0000202112
-
JP-HHT
-
Unknown
12y
-
-
-
-
Benjamin Tschupp
00264266
0000202113
-
JP-HHT
-
Isolated (sporadic)
6y
-
-
-
-
Benjamin Tschupp
00264267
0000202114
-
JP-HHT
-
Familial
28y
-
-
-
-
Benjamin Tschupp
00264268
0000301955
Telangiectasia (HP:0001009), Epistaxis (HP:0000421), Cavernous hemangioma (HP:0001048)
JPS and JPHT
JPS and JPHT
Unknown
08y
08y
08y
-
-
Litika Vermani
00409839
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