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Phenotypes for disease #00002 (JBTS1 (Joubert syndrome, type 1 (JBTS1)), OMIM:213300)
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
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
Diagnosis/Definite
: phenotype individual after molecular testing (OMIM abbreviation)
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
How to query this table
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Column type
Example
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Arg
all entries containing 'Arg'
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!
Text
!fs
all entries not containing 'fs'
^
Text
^p.(Arg
all entries beginning with 'p.(Arg'
$
Text
Ser)$
all entries ending with 'Ser)'
=""
Text
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="p.0"
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combination
Text
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Date
2020
all entries matching the year 2020
|
Date
2020-03|2020-04
all entries matching March or April, 2020
!
Date
!2020-03
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
<=2020-06
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>
Date
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all entries after June, 2020
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Date
>=2020-06-15
all entries on or after June 15th, 2020
combination
Date
2019|2020 <2020-03
all entries in 2019 or 2020, and before March, 2020
Numeric
23
all entries exactly matching 23
|
Numeric
23|24
all entries exactly matching 23 or 24
!
Numeric
!23
all entries not exactly matching 23
<
Numeric
<23
all entries lower than 23
<=
Numeric
<=23
all entries lower than, or equal to, 23
>
Numeric
>23
all entries higher than 23
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Numeric
>=23
all entries higher than, or equal to, 23
combination
Numeric
>=20 <30 !23
all entries with values from 20 to 29, but not equal to 23
Some more advanced examples:
Example
Matches
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all entries containing 'Asian', 'asian', including 'Caucasian', 'caucasian', etc.
Asian !Caucasian
all entries containing 'Asian' but not containing 'Caucasian'
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all entries containing 'Asian' or 'African', but not containing 'Caucasian'
"South Asian"
all entries containing 'South Asian', but not containing 'South East Asian'
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53 entries on 1 page. Showing entries 1 - 53.
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Legend
How to query
Phenotype ID
Phenotype details
Diagnosis/Initial
Inheritance
Age/Examination
Diagnosis/Definite
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000002016
infantile spasms, ECG-hypsarrhythmia, mental retardation, epilepsy
-
Familial, X-linked recessive
-
-
-
-
-
-
Johan den Dunnen
00003176
0000002088
-
-
Isolated (sporadic)
-
-
-
-
-
-
Johan den Dunnen
00003249
0000015971
-
-
Familial, autosomal recessive
02y06m
-
-
-
-
-
Tania Attie-Bitach
00017612
0000016041
Polydactyly, postaxial (left foot); Delayed psychomotor development; hypotonia; enlargement of the fourth ventricle, ´molar tooth sign´
-
Familial, autosomal recessive
00y00m
-
-
-
-
-
Valeska Frank
00017648
0000016134
cerebellar vermis aplasia, hypotonia, no evidence renal disease
-
Isolated (sporadic)
06y
-
-
-
-
-
Johan den Dunnen
00017798
0000016135
gross motor/communication delays, increased tone/reflexes, bilateral talipes equinovarus deformity (clubfeet); 15m no evidence cardiovascular/renal/liver disease (ultrasound, laboratory testing, brain MRI revealed molar tooth sign
-
Isolated (sporadic)
-
-
-
-
-
-
Johan den Dunnen
00017799
0000016136
all 4 childhood-onset Joubert Syndrome, extremely poor learning abilities; brain MRI molar tooth sign
-
Familial, autosomal recessive
-
-
-
-
-
-
Johan den Dunnen
00017800
0000016160
Polydactyly, postaxial; Delayed psychomotor development; hypotonia; frontally pronounced polymicrogyria, cerebellar hypoplasia and myelinisation defects; nystagmus and hyperopia; ´molar tooth sign´; ataxia
-
Familial, autosomal recessive
00y00m
-
-
-
-
-
Valeska Frank
00017626
0000021242
-
-
Unknown
-
-
-
-
-
-
Hanno Bolz
00016591
0000023263
see paper; cerebellar dysplasia, cerebellar cysts, global vermis hypoplasia, ...
-
Familial, autosomal recessive
>23y
-
-
-
-
-
Johan den Dunnen
00027191
0000023264
see paper; mild Joubert syndrome, cerebellar dysplasia (superior only), no cerebellar cysts, global vermis hypoplasia (inferior only), ...
-
Familial, autosomal recessive
>00y05m
-
-
-
-
-
Johan den Dunnen
00027192
0000025006
-
-
Unknown
-
-
-
-
-
-
Sanne Savelberg
00028926
0000025008
-
-
Unknown
-
-
-
-
-
-
Sanne Savelberg
00028912
0000025009
-
-
Unknown
-
-
-
-
-
-
Sanne Savelberg
00028913
0000025010
-
-
Unknown
-
-
-
-
-
-
Sanne Savelberg
00028914
0000025011
-
-
Unknown
-
-
-
-
-
-
Sanne Savelberg
00028915
0000025012
-
-
Unknown
-
-
-
-
-
-
Sanne Savelberg
00028916
0000025013
-
-
Unknown
-
-
-
-
-
-
Sanne Savelberg
00028917
0000025014
-
-
Unknown
-
-
-
-
-
-
Sanne Savelberg
00028918
0000025015
-
-
Unknown
-
-
-
-
-
-
Sanne Savelberg
00028919
0000025016
-
-
Unknown
-
-
-
-
-
-
Sanne Savelberg
00028920
0000025017
-
-
Unknown
-
-
-
-
-
-
Sanne Savelberg
00028921
0000025018
-
-
Unknown
-
-
-
-
-
-
Sanne Savelberg
00028922
0000025019
-
-
Unknown
-
-
-
-
-
-
Sanne Savelberg
00028923
0000025020
-
-
Unknown
-
-
-
-
-
-
Sanne Savelberg
00028924
0000025021
-
-
Unknown
-
-
-
-
-
-
Sanne Savelberg
00028925
0000025022
-
-
Unknown
-
-
-
-
-
-
Sanne Savelberg
00028947
0000025023
-
-
Unknown
-
-
-
-
-
-
Sanne Savelberg
00028948
0000025024
-
-
Unknown
-
-
-
-
-
-
Sanne Savelberg
00028949
0000025025
-
-
Isolated (sporadic)
-
-
-
-
-
-
Sanne Savelberg
00028950
0000025026
-
-
Isolated (sporadic)
-
-
-
-
-
-
Sanne Savelberg
00028951
0000025027
-
-
Isolated (sporadic)
-
-
-
-
-
-
Sanne Savelberg
00028952
0000026510
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00033081
0000026515
-
-
Unknown
-
-
-
-
-
-
Johan den Dunnen
00033086
0000026764
-
-
Isolated (sporadic)
-
-
-
-
-
-
Anas M Alazami
00033335
0000026765
-
-
Isolated (sporadic)
-
-
-
-
-
-
Anas M Alazami
00033336
0000026766
-
-
Isolated (sporadic)
-
-
-
-
-
-
Anas M Alazami
00033337
0000026767
-
-
Isolated (sporadic)
-
-
-
-
-
-
Anas M Alazami
00033338
0000043044
-
-
Unknown
-
-
-
-
-
-
Hester Y. Kroes
00019401
0000043045
-
-
Unknown
-
-
-
-
-
-
Hester Y. Kroes
00019402
0000043046
-
-
Unknown
-
-
-
-
-
-
Hester Y. Kroes
00019403
0000043047
-
-
Unknown
-
-
-
-
-
-
Hester Y. Kroes
00019404
0000043048
-
-
Unknown
-
-
-
-
-
-
Hester Y. Kroes
00019405
0000043049
-
-
Unknown
-
-
-
-
-
-
Hester Y. Kroes
00019406
0000043050
-
-
Unknown
-
-
-
-
-
-
Hester Y. Kroes
00019400
0000043051
-
-
Unknown
-
-
-
-
-
-
Hester Y. Kroes
00019407
0000043052
-
-
Unknown
-
-
-
-
-
-
Hester Y. Kroes
00019408
0000085351
autosomal dominant osteosclerosis
-
Familial, autosomal dominant
-
-
-
-
-
-
Johan den Dunnen
00107586
0000085352
autosomal dominant osteosclerosis
-
Familial, autosomal dominant
-
-
-
-
-
-
Johan den Dunnen
00107587
0000186548
FTLD
-
Familial
-
-
-
-
-
-
Serena Lattante
00246721
0000186551
FTLD
-
Familial
-
-
-
54y
-
-
Serena Lattante
00246724
0000199363
IMD28; IFNGR2 deficiency; MSMD
-
Familial, autosomal recessive
-
-
-
-
-
-
LOVD
00260831
0000203419
HP:0001263 HP:0001251 HP:0001249 HP:0002553 HP:0000508 HP:0000657 HP:0002793 HP:0001252 HP:0001320 HP:0100951 HP:0002419 HP:0000007
Cerebral palsy
Familial, autosomal recessive
10y
Joubert syndrome
10y
02y
-
-
Minh Tuan Huynh
00265632
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