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Phenotypes for disease #00525 (Crouzon (Crouzon syndrome), OMIM:123500)
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
How to query this table
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Column type
Example
Matches
Text
Arg
all entries containing 'Arg'
space
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|
Text
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Text
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all entries not containing 'fs'
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Text
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all entries beginning with 'p.(Arg'
$
Text
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all entries ending with 'Ser)'
=""
Text
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Text
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Text
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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
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Date
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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
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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
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
>=
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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29 entries on 1 page. Showing entries 1 - 29.
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Legend
How to query
Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000017618
-
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00017818
0000017619
-
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00017819
0000017620
-
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00019775
0000017621
-
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00019776
0000017622
-
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00019777
0000017623
-
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00019778
0000017626
-
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00019779
0000017630
-
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00019781
0000017631
-
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00019782
0000017632
-
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00019783
0000017633
-
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00019788
0000017635
-
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00019789
0000017636
-
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00019790
0000017637
-
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00019792
0000017638
-
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00019793
0000017639
-
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00019794
0000017640
-
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00019795
0000017641
-
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00019827
0000017642
-
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00019828
0000017643
-
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00019829
0000017644
-
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00019830
0000017645
-
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00019831
0000017663
-
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00019826
0000017670
Crouzon syndrome with acanthosis nigricans
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00019816
0000017671
Crouzon syndrome with acanthosis nigricans
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00019817
0000017672
Crouzon syndrome with acanthosis nigricans
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00019818
0000017673
Crouzon syndrome with acanthosis nigricans
-
-
Unknown
-
-
-
-
-
Karen E. Heath
00019819
0000252754
-
-
Crouzon Syndrome
Familial, autosomal dominant
-
06y
-
-
-
Malak Alghamdi
00335046
0000254046
Crouzon syndrome, craniosynostosis, scoliosis, exophthalmos, limited elbow extension, right eye almost blind, left eye visual acuity approx. 2%, no hearing loss, father, brother and his daughter also affected.
-
-
Familial, autosomal dominant
54y
-
-
-
-
Andreas Laner
00358831
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