Global Variome shared LOVD
IL2RA (interleukin 2 receptor, alpha)
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Phenotypes for disease #02221 (CPDX1 (chondrodysplasia punctata, type 1, X-linked recessive (CPDX-1)), OMIM:302950)
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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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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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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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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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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 'Asian' or 'African', 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
0000090190
CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114708
0000090192
Respiratory insufficiency and feeding problems at birth. Nasal hypoplasia, single palmar crease and small tufted distal phalanges.; CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114710
0000090193
Midface hypoplasia, brachytelephalangy; CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114711
0000090194
CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114712
0000090195
CPDX1
-
-
Unknown
-
-
-
-
-
Gene Dx
00114713
0000090199
CPDX1
-
-
Unknown
-
-
-
-
-
Gene Dx
00114717
0000090201
CPDX1
-
-
Unknown
-
-
-
-
-
Gene Dx
00114719
0000090202
CPDX1
-
-
Unknown
-
-
-
-
-
Gene Dx
00114720
0000090203
Microcephaly, flat nose, short stature, puncta in the feet, hands and sacrum; CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114721
0000090210
CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114728
0000090211
CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114729
0000090212
CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114730
0000090213
CPDX1
-
-
Unknown
-
-
-
-
-
Gene Dx
00114731
0000090214
CPDX1
-
-
Unknown
-
-
-
-
-
Gene Dx
00114732
0000090215
CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114733
0000090216
CPDX1
-
-
Unknown
-
-
-
-
-
Gene Dx
00114734
0000090218
Nasal hypoplasia, brachytelephalang; CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114736
0000090220
CPDX1
-
-
Unknown
-
-
-
-
-
Gene Dx
00114738
0000090221
Nasal hypoplasia, brachytelephalangy; CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114739
0000090222
No detailed patient information was given. However it is mentioned that typical radiological and clinical features for CDPX1 were met
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114740
0000090224
No detailed patient information was given. However it is mentioned that typical radiological and clinical features for CDPX1 were met
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114742
0000090225
CPDX1
-
-
Unknown
-
-
-
-
-
Gene Dx
00114743
0000090226
Flat nose, brachytelephalangic chondrodysplasia, left school at 9 yo due to poor school perfomance. Maternal grandfather is positive for the same mutation but he is asymptomatic); CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114744
0000090227
CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114745
0000090229
CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114747
0000090231
No detailed patient information was given. However it is mentioned that typical radiological and clinical features for CDPX1 were met ; CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114749
0000090233
CPDX1
-
-
Unknown
-
-
-
-
-
Gene Dx
00114751
0000090236
No detailed patient information was given. However it is mentioned that typical radiological and clinical features for CDPX1 were met ; CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114754
0000090238
CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114756
0000090241
CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114759
0000090242
CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114760
0000090244
CPDX1
-
-
Unknown
-
-
-
-
-
Gene Dx
00114762
0000090245
Flat nose, brachytelephalangic chondrodysplasia ; CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114763
0000090247
CPDX1
-
-
Unknown
-
-
-
-
-
Gene Dx
00114765
0000090248
CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114766
0000090249
CPDX1
-
-
Unknown
-
-
-
-
-
Gene Dx
00114767
0000090250
CPDX1
-
-
Unknown
-
-
-
-
-
Gene Dx
00114768
0000090252
CPDX1
-
-
Unknown
-
-
-
-
-
Gene Dx
00114770
0000090254
CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114772
0000090256
Calcification of larynx, joint contractures; CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114774
0000090258
CPDX1
-
-
Unknown
-
-
-
-
-
Gene Dx
00114776
0000090260
CPDX1
-
-
Unknown
-
-
-
-
-
Gene Dx
00114778
0000090261
Midface hypoplasia, brachytelephalangy, punctate calcifications at the X-ray skeletal survery ; CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114779
0000090262
CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114780
0000090263
CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114781
0000090264
CPDX1
-
-
Unknown
-
-
-
-
-
Gene Dx
00114782
0000090266
CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114784
0000090268
Nasal hypoplasia, brachytelephalangy, punctate calcifications at the X-ray skeletal survery and deafness; CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114786
0000090269
Neonatal death, facial dysmorphisms, brachytelephalangy, cararact, disseminated intravascular coagulopathy ; CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114787
0000090270
CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114788
0000090272
CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114790
0000090273
CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114791
0000090277
Aborted fetus of 26 weeks with severe nasal hypoplasia, short hands and fingers. X-ray diffuse calcifications of epiphyses, spine and larynx. Absent fusion of the three primitive nasal stalks ; CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114795
0000090278
Nasal hypoplasia, flat midface, brachytelephalangy, punctate calcifications at the X-ray skeletal survery. Multiple coronal clefts of vertebrae. Laryngeal calcifications ; CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114796
0000090279
Nasal hypoplasia, diffuse calcifications of trachea and bronchi. Recurrent and severe episodes of respiratory insufficiency ; CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114797
0000090280
Midface hypoplasia, brachytelephalangy, punctate calcifications at the X-ray skeletal survery ; CPDX1
-
-
Unknown
-
-
-
-
-
Claudia Matos-Miranda
00114798
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