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Phenotypes for disease #00949 (craniosynost. (craniosynostosis, nonspecific))
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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Date
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14 entries on 1 page. Showing entries 1 - 14.
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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
0000049862
bicoronal suture synostosis myopia divergent growth pattern and crowding of teeth normal development
-
-
Familial, autosomal dominant
-
5M
-
birth
-
Jacqueline Goos
00063258
0000049863
Fusion of all calvarial sutures (except metopic) Increased intracranial pressure
-
-
Familial, autosomal dominant
-
6M
-
birth
-
Jacqueline Goos
00063259
0000049864
Bicoronal suture synostosis Small ears with prominent crura Marked bilateral 5th finger clinodactyly Class II.1 dental malocclusion Normal development
-
-
Familial, autosomal dominant
-
10.5M
-
birth
-
Jacqueline Goos
00063260
0000127075
Craniosynostosis, Low anterior hairline, Long eyelashes, Wide nose, Restlessness, Expressive language delay, Receptive language delay, Global developmental delay, Obesity
-
-
Unknown
05y
-
-
-
-
Andreas Laner
00154400
0000270751
craniosynostosis, metopic suture
-
-
Familial, autosomal recessive
-
-
00y
-
-
Jacqueline Goos
00375537
0000292893
see paper; ..., craniosynostosis; severe branchio-otic syndrome; affected sutures sgittal, lambdoid (left, right); speech/language delay, ear pits/tags, unilateral neck sinus, sensorineural hearing loss
craniosynostosis
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00399853
0000292894
see paper; ..., craniosynostosis; no branchio-otic syndrome; affected sutures sgittal; borderline short stature, mild anteverted nares
craniosynostosis
-
Familial
-
-
-
-
-
Johan den Dunnen
00399854
0000292895
see paper; ..., craniosynostosis; severe branchio-otic syndrome; affected sutures sgittal, lambdoid (left, right); branchial fistula
craniosynostosis
-
Familial
-
-
-
-
-
Johan den Dunnen
00399855
0000292896
see paper; ..., craniosynostosis; severe branchio-otic syndrome; affected sutures coronal (left, right), sagittal; branchial fistula, restricted growth, posterior urethral valves
craniosynostosis
-
Familial
-
-
-
-
-
Johan den Dunnen
00399856
0000292897
see paper; ..., craniosynostosis; severe branchio-otic syndrome; affected sutures sgittal, lambdoid (left, right); mild conductive hearing loss, unilateral branchial cyst/fistula
craniosynostosis
-
Familial
-
-
-
-
-
Johan den Dunnen
00399857
0000292898
see paper; ..., craniosynostosis; no branchio-otic syndrome; affected sutures sgittal, lambdoid (left, right)
craniosynostosis
-
Familial
-
-
-
-
-
Johan den Dunnen
00399858
0000292899
see paper; ..., craniosynostosis; mild branchio-otic syndrome; affected sutures sgittal; preauricular pits
craniosynostosis
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00399859
0000292900
see paper; ..., craniosynostosis; mild branchio-otic syndrome; affected sutures sgittal; occult bilateral branchial cysts
craniosynostosis
-
Familial
-
-
-
-
-
Johan den Dunnen
00399860
0000338889
dystrophic toenail, hypotelorism, intrauterine growth retardation, moderate global developmental delay, postnatal microcephaly and recurrent infections
-
microcephaly, developmental delay and skeletal anomalies (MISA syndrome)
Unknown
-
-
-
-
-
Carmela Fusco
00449719
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