Global Variome shared LOVD
IL15RA (interleukin 15 receptor, alpha)
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Phenotypes for disease #00161 (IP (incontinentia pigmenti (IP)), OMIM:308300)
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.
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
Phenotype details
: additional information on the phenotype of the individual, preferably use HPO terms only (http://www.human-phenotype-ontology.org/)
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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Date
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Date
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61 entries on 1 page. Showing entries 1 - 61.
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Legend
How to query
Phenotype ID
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Phenotype details
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000232039
-
-
Familial, autosomal dominant
-
-
-
-
-
-
Sha Hong
00306192
0000232040
-
-
Familial, X-linked dominant
-
-
-
-
-
-
Sha Hong
00306192
0000247314
incontinentia pigmenti
-
Isolated (sporadic)
see paper; ...
-
-
-
-
-
Johan den Dunnen
00329116
0000247315
incontinentia pigmenti
IP
Isolated (sporadic)
see paper; ...
-
-
-
-
-
Johan den Dunnen
00329117
0000247341
incontinentia pigmenti
IP
Familial, autosomal dominant
-
-
-
-
-
-
Johan den Dunnen
00001436
0000247342
incontinentia pigmenti
IP
Familial, autosomal dominant
skin pigmentation, conical teeth, retinal detachment, alopecia, CNS problems
-
-
-
-
-
Johan den Dunnen
00329152
0000247343
incontinentia pigmenti
IP
Familial, autosomal dominant
skin pigmentation, conical teeth, retinal detachment, alopecia, CNS problems
-
-
-
-
-
Johan den Dunnen
00329153
0000247344
incontinentia pigmenti
IP
Familial, autosomal dominant
skin pigmentation, conical teeth, retinal detachment, alopecia, CNS problems
-
-
-
-
-
Johan den Dunnen
00001433
0000247345
incontinentia pigmenti
IP
Familial, autosomal dominant
-
-
-
-
-
-
Johan den Dunnen
00329154
0000247346
incontinentia pigmenti
IP
Familial, autosomal dominant
skin pigmentation, conical teeth, retinal detachment, alopecia, CNS problems
-
-
-
-
-
Johan den Dunnen
00329155
0000247347
incontinentia pigmenti
IP
Familial, autosomal dominant
-
-
-
-
-
-
Johan den Dunnen
00001435
0000247349
incontinetia pigmenti
IP
Familial, autosomal dominant
-
-
-
-
-
-
Johan den Dunnen
00329165
0000247350
incontinetia pigmenti
IP
Isolated (sporadic)
-
-
-
-
-
-
Johan den Dunnen
00329166
0000247351
incontinetia pigmenti
IP
Familial, autosomal dominant
-
-
-
-
-
-
Johan den Dunnen
00329167
0000247352
incontinetia pigmenti
IP
Familial, autosomal dominant
-
-
-
-
-
-
Johan den Dunnen
00329168
0000247361
incontinentia pigmenti
IP
Familial, X-linked recessive
see paper; ..., recurrent infections, immune deficiency; 12y10m-died from herpes simplex virus 1 meningo-encephalitis
-
-
00y15m
-
-
Johan den Dunnen
00329164
0000247362
incontinentia pigmenti
IP
Familial, autosomal dominant
see paper; ..., severe incontinentia pigmenti
-
-
-
-
-
Johan den Dunnen
00001461
0000247363
incontinentia pigmenti
IP
Familial, X-linked recessive
see paper; ..., incontinentia pigmenti, osteopetrosis, lymphedema, ectodermal dysplasia, immune deficiency
-
-
-
-
-
Johan den Dunnen
00001467
0000247364
incontinentia pigmenti
IP
Familial, autosomal dominant
incontinentia pigmenti, ectodermal dysplasia, immune deficiency
-
-
-
-
-
Johan den Dunnen
00001463
0000247365
incontinentia pigmenti
IP
Familial, autosomal dominant
incontinentia pigmenti
-
-
-
-
-
Johan den Dunnen
00001414
0000247366
incontinentia pigmenti
IP
Familial, autosomal dominant
ectodermal dysplasia, immune deficiency
-
-
-
-
-
Johan den Dunnen
00329170
0000247368
incontinentia pigmenti
-
Familial, X-linked recessive
hypohidrotic ectodermal dysplasia, immunodeficiency
-
-
-
-
-
Johan den Dunnen
00329173
0000247369
-
-
Familial, X-linked recessive
hypohidrotic ectodermal dysplasia, immunodeficiency
-
-
-
-
-
Johan den Dunnen
00329174
0000247370
-
-
Familial, X-linked recessive
hypohidrotic ectodermal dysplasia, immunodeficiency
-
-
-
-
-
Johan den Dunnen
00329175
0000247372
incontinentia pigmenti
-
Familial, X-linked dominant
see papr; ..., incontinentia pigmenti, osteopetrosis, lymphedema, ectodermal dysplasia, immune deficiency
-
-
-
-
-
Johan den Dunnen
00329177
0000247373
incontinentia pigmenti
-
Familial, X-linked dominant
see paper; ..., incontinentia pigmenti, ectodermal dysplasia, immune deficiency
-
-
-
-
-
Johan den Dunnen
00329178
0000247374
incontinentia pigmenti
-
Familial, X-linked
see paper; ..., incontinentia pigmenti, ectodermal dysplasia, immune deficiency
-
-
-
-
-
Johan den Dunnen
00329179
0000247375
incontinentia pigmenti
-
Familial, X-linked
see paper; ..., incontinentia pigmenti, ectodermal dysplasia, immune deficiency
-
-
-
-
-
Johan den Dunnen
00329180
0000247376
incontinentia pigmenti
-
Familial, X-linked
see paper; ..., incontinentia pigmenti, ectodermal dysplasia, immune deficiency
-
-
-
-
-
Johan den Dunnen
00329181
0000247377
incontinentia pigmenti
-
Familial, X-linked
see paper; ..., incontinentia pigmenti, ectodermal dysplasia, immune deficiency
-
-
-
-
-
Johan den Dunnen
00329182
0000247378
incontinentia pigmenti
-
Familial, X-linked
see paper; ..., incontinentia pigmenti, ectodermal dysplasia, immune deficiency
-
-
-
-
-
Johan den Dunnen
00329183
0000247379
incontinentia pigmenti
-
Familial, X-linked
see paper; ..., incontinentia pigmenti, ectodermal dysplasia, immune deficiency
-
-
-
-
-
Johan den Dunnen
00329184
0000247380
incontinentia pigmenti
-
Familial, X-linked
see paper; ..., incontinentia pigmenti, ectodermal dysplasia, immune deficiency
-
-
-
-
-
Johan den Dunnen
00329185
0000247385
incontinentia pigmenti
IP
Familial, X-linked dominant
see paper; ...
-
-
-
-
-
Johan den Dunnen
00329190
0000247386
incontinentia pigmenti
IP
Familial, X-linked dominant
see paper; ...
-
-
-
-
-
Johan den Dunnen
00329191
0000247387
incontinentia pigmenti
IP
Familial, X-linked dominant
see paper; ...
-
-
-
-
-
Johan den Dunnen
00329192
0000247388
incontinentia pigmenti
IP
Familial, X-linked dominant
see paper; ...
-
-
-
-
-
Johan den Dunnen
00329193
0000247389
incontinentia pigmenti
IP
Familial, X-linked dominant
see paper; ...
-
-
-
-
-
Johan den Dunnen
00329194
0000247390
incontinentia pigmenti
IP
Familial, X-linked dominant
see paper; ...
-
-
-
-
-
Johan den Dunnen
00329195
0000247391
incontinentia pigmenti
IP
Familial, X-linked dominant
see paper; ...
-
-
-
-
-
Johan den Dunnen
00329196
0000247392
incontinentia pigmenti
IP
Familial, X-linked dominant
see paper; ...
-
-
-
-
-
Johan den Dunnen
00329197
0000249034
incontinetia pigmenti
IP
Familial, autosomal dominant
-
-
-
-
-
-
Johan den Dunnen
00330841
0000249035
incontinetia pigmenti
IP
Familial, autosomal dominant
-
-
-
-
-
-
Johan den Dunnen
00330842
0000249036
incontinetia pigmenti
IP
Familial, autosomal dominant
-
-
-
-
-
-
Johan den Dunnen
00330843
0000249037
incontinetia pigmenti
IP
Familial, autosomal dominant
-
-
-
-
-
-
Johan den Dunnen
00330844
0000249038
incontinetia pigmenti
IP
Familial, autosomal dominant
-
-
-
-
-
-
Johan den Dunnen
00330845
0000249039
incontinetia pigmenti
IP
Familial, autosomal dominant
-
-
-
-
-
-
Johan den Dunnen
00330846
0000249040
incontinetia pigmenti
IP
Familial, autosomal dominant
-
-
-
-
-
-
Johan den Dunnen
00330847
0000249041
incontinetia pigmenti
IP
Familial, autosomal dominant
-
-
-
-
-
-
Johan den Dunnen
00330848
0000249042
incontinetia pigmenti
IP
Familial, autosomal dominant
-
-
-
-
-
-
Johan den Dunnen
00330849
0000249043
incontinetia pigmenti
IP
Familial, autosomal dominant
-
-
-
-
-
-
Johan den Dunnen
00330850
0000249044
incontinetia pigmenti
IP
Familial, autosomal dominant
-
-
-
-
-
-
Johan den Dunnen
00330851
0000249045
incontinetia pigmenti
IP
Familial, autosomal dominant
-
-
-
-
-
-
Johan den Dunnen
00330852
0000249046
incontinetia pigmenti
IP
Familial, autosomal dominant
-
-
-
-
-
-
Johan den Dunnen
00330853
0000249048
incontinetia pigmenti
IP
Familial, autosomal dominant
-
-
-
-
-
-
Johan den Dunnen
00330855
0000249049
incontinetia pigmenti
IP
Familial, autosomal dominant
-
-
-
-
-
-
Johan den Dunnen
00330856
0000249050
incontinetia pigmenti
IP
Familial, autosomal dominant
-
-
-
-
-
-
Johan den Dunnen
00330857
0000249051
incontinetia pigmenti
IP
Familial, autosomal dominant
-
-
-
-
-
-
Johan den Dunnen
00330858
0000314455
incontinentia pigmenti
IP
Isolated (sporadic)
see paper; ..., birth few blisters and erythema in upper arms
-
-
-
-
-
Johan den Dunnen
00409989
0000314456
incontinentia pigmenti
IP
Unknown
see paper
-
-
-
-
-
Miki Kawai, Hiroki Kurahashi
00275680
0000325281
incontinentia pigmenti
IP
Familial, X-linked dominant
see paper
27y
-
-
-
-
Johan den Dunnen
00435042
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