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Phenotypes for disease #04327 (CRS (craniosynostosis (CRS)))
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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Text
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all entries beginning with 'p.(Arg'
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Date
2020
all entries matching the year 2020
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Date
2020-03|2020-04
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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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
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all entries exactly matching 23
|
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 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' 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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46 entries on 1 page. Showing entries 1 - 46.
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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
0000036723
nicoronal synostosis also present in mother
-
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00050112
0000049861
Right coronal suture synostosis bilateral camptodactyly of the fifth fingers divergent strabismus recurrent airway infections mild learning problems
-
-
Familial, autosomal dominant
-
4.5m
00y00m00d
birth
-
Jacqueline Goos
00063257
0000058844
-
-
-
Unknown
-
-
-
-
-
Kerry Miller
00079117
0000058845
Flat mid-face, down-slanting palpebral fissures, low set ears, facial asymmetry, retracted pre-maxilla, right choanal stenosis, micrognathia, peg-like teeth with conical incisors, absent lateral incisors, pectus excavatum, scoliosis, long palms, slight digital shortening, mild 4/5 syndactyly of toes, Chiari malformation, moderate - severe learning difficulties.
-
-
Isolated (sporadic)
-
-
-
-
-
Kerry Miller
00079118
0000058846
Learning difficulties
-
-
Isolated (sporadic)
-
-
-
-
-
Kerry Miller
00079119
0000125628
bicoronal synostosis (HP:0011318), sagittal craniosynostosis (HP:0004442)
craniosynostosis affecting bilateral coronal and sagittal sutures
-
Unknown
-
-
-
-
-
Anshuman Sewda
00152044
0000125629
bicoronal synostosis (HP:0011318)
craniosynostosis affecting bilateral coronal sutures
-
Unknown
-
-
-
-
-
Anshuman Sewda
00152526
0000125630
unicoronal synostosis, left (HP:0011315)
craniosynostosis affecting left coronal sutures
-
Unknown
-
-
-
-
-
Anshuman Sewda
00152529
0000125631
unicoronal synostosis, left (HP:0011315)
craniosynostosis affecting left coronal sutures
-
Unknown
-
-
-
-
-
Anshuman Sewda
00152003
0000125632
unicoronal synostosis, right (HP:0011315)
craniosynostosis affecting right coronal sutures
-
Unknown
-
-
-
-
-
Anshuman Sewda
00152528
0000125633
sagittal craniosynostosis (HP:0004442)
sagittal craniosynostosis
-
Unknown
-
-
-
-
-
Anshuman Sewda
00152530
0000125634
sagittal craniosynostosis (HP:0004442)
sagittal craniosynostosis
-
Unknown
-
-
-
-
-
Anshuman Sewda
00152527
0000125635
sagittal craniosynostosis (HP:0004442)
sagittal craniosynostosis
-
Unknown
-
-
-
-
-
Anshuman Sewda
00152011
0000219686
see paper; ..., neonatal microcephaly, agenesis corpus callosum, brachycephaly with reduced volume posterior fossa, cerebellar and pons hypoplasia, scoliosis, tethered cord (closed neural tube defect)
craniosynostosis
BAIDCS
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00285854
0000219687
see paper; ..., neonatal microcephaly, agenesis corpus callosum, brachycephaly with reduced volume posterior fossa, cerebellar and pons hypoplasia, scoliosis, tethered cord (closed neural tube defect)
craniosynostosis
BAIDCS
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00285855
0000219729
mother cranial dysmorphism; two children sagittal craniosynostosis
craniosynostosis
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00285887
0000219730
sagittal craniosynostosis
craniosynostosis
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00285888
0000219731
sporadic metopic craniosynostosis
craniosynostosis
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00285889
0000219764
sagittal craniosynostosis, metopic craniosynostosis
craniosynostosis
-
Di-genic
-
-
-
-
-
Johan den Dunnen
00285891
0000219765
sagittal craniosynostosis
craniosynostosis
-
Di-genic
-
-
-
-
-
Johan den Dunnen
00285892
0000219766
sagittal craniosynostosis, metopic craniosynostosis
craniosynostosis
-
Di-genic
-
-
-
-
-
Johan den Dunnen
00285893
0000219767
sagittal craniosynostosis
craniosynostosis
-
Di-genic
-
-
-
-
-
Johan den Dunnen
00285894
0000219768
sagittal craniosynostosis
craniosynostosis
-
Di-genic
-
-
-
-
-
Johan den Dunnen
00285895
0000219769
sagittal craniosynostosis
craniosynostosis
-
Di-genic
-
-
-
-
-
Johan den Dunnen
00285896
0000219770
metopic craniosynostosis
craniosynostosis
-
Di-genic
-
-
-
-
-
Johan den Dunnen
00285897
0000219771
metopic craniosynostosis
craniosynostosis
-
Di-genic
-
-
-
-
-
Johan den Dunnen
00285898
0000219772
metopic craniosynostosis
craniosynostosis
-
Di-genic
-
-
-
-
-
Johan den Dunnen
00285899
0000219773
metopic craniosynostosis
craniosynostosis
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00285900
0000219774
metopic craniosynostosis
craniosynostosis
-
Di-genic
-
-
-
-
-
Johan den Dunnen
00285901
0000219775
metopic craniosynostosis
craniosynostosis
-
Di-genic
-
-
-
-
-
Johan den Dunnen
00285902
0000219776
metopic craniosynostosis
craniosynostosis
-
Di-genic
-
-
-
-
-
Johan den Dunnen
00285903
0000219777
-
-
-
Di-genic
-
-
-
-
-
Johan den Dunnen
00285904
0000219778
-
-
-
Di-genic
-
-
-
-
-
Johan den Dunnen
00285905
0000219781
sagittal craniosynostosis
craniosynostosis
-
Di-genic
-
-
-
-
-
Johan den Dunnen
00285908
0000219783
metopic craniosynostosis
craniosynostosis
-
Di-genic
-
-
-
-
-
Johan den Dunnen
00285910
0000219794
see paper; ..., sagittal craniosynostosis, coronal craniosynostosis, recurrence of CS within two months initial surgery requiring second operatio
craniosynostosis
-
Di-genic
-
-
-
-
-
Johan den Dunnen
00285921
0000219795
metopic craniosynostosis
craniosynostosis
-
Di-genic
-
-
-
-
-
Johan den Dunnen
00285923
0000219796
metopic craniosynostosis
craniosynostosis
-
Di-genic
-
-
-
-
-
Johan den Dunnen
00285927
0000219797
metopic craniosynostosis
craniosynostosis
-
Di-genic
-
-
-
-
-
Johan den Dunnen
00285929
0000219798
metopic craniosynostosis
craniosynostosis
-
Di-genic
-
-
-
-
-
Johan den Dunnen
00285932
0000268614
-
-
-
Isolated (sporadic)
-
-
-
-
-
Stuart Scott
00373335
0000326766
see paper; ..., hypoplasia or abscent corpus callosum, ventriculomegaly, lambdoid craniosynostosis, macrocephaly, develomental delay, dysmorphic features, no urinary tract defects
craniosynostosis
BRMUTD
Familial, autosomal dominant
13y
-
-
-
-
Johan den Dunnen
00436630
0000326767
see paper; ..., hypoplasia or abscent corpus callosum, ventriculomegaly, no craniosynostosis, macrocephaly, develomental delay, dysmorphic features, urinary tract defects
craniosynostosis
BRMUTD
Familial, autosomal dominant
10y
-
-
-
-
Johan den Dunnen
00436631
0000326768
see paper; ..., hypoplasia or abscent corpus callosum, ventriculomegaly, lambdoid craniosynostosis, macrocephaly, develomental delay, dysmorphic features, no urinary tract defects
craniosynostosis
BRMUTD
Familial, autosomal dominant
6y
-
-
-
-
Johan den Dunnen
00436632
0000326769
see paper; ..., hypoplasia or abscent corpus callosum, no ventriculomegaly, sagittal craniosynostosis, macrocephaly, no develomental delay, no dysmorphic features, urinary tract defects
craniosynostosis
BRMUTD
Familial, autosomal dominant
42y
-
-
-
-
Johan den Dunnen
00436633
0000338888
true hypotelorism, severe microcephaly, residual retrognathia, high arched palate with bifid uvula, dental crowding, mild scoliosis and generalized joint hypermobility with Beighton score 6/9, cleft palate
-
microcephaly, developmental delay and skeletal anomalies (MISA syndrome)
Familial, autosomal dominant
-
-
-
-
-
Carmela Fusco
00449718
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