Global Variome shared LOVD
APC (adenomatous polyposis coli)
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Curators:
Stefan Aretz
,
Isabel Spier
, and
Xiaoyu Sherry Yin
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Phenotypes for disease #05397 (CCM1 (cerebral cavernous malformations, type 1), OMIM:116860)
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.
Diagnosis/Initial
: initial diagnosis, before molecular testing
Diagnosis/Definite
: phenotype individual after molecular testing (OMIM abbreviation)
Phenotype details
: additional information on the phenotype of the individual, preferably use HPO terms only (http://www.human-phenotype-ontology.org/)
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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Date
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Date
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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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25 entries on 1 page. Showing entries 1 - 25.
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How to query
Phenotype ID
Diagnosis/Initial
Diagnosis/Definite
Phenotype details
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000129957
CCM
CCM
-
Familial, autosomal dominant
-
-
-
-
-
Carmela Fusco
00165057
0000130556
cerebral cavernous malformations
CCM-1
-
Familial, autosomal dominant
-
-
-
-
-
Carmela Fusco
00165692
0000130557
cerebral cavernous malformations
CCM1
headache/migraine (HP:0002076); hemiparesis (HP:0001269); sovratentorial hemangiomas; cerebellar hemangiomas; bilateral lesions
Isolated (sporadic)
51y
-
45y
-
-
Carmela Fusco
00165693
0000130558
cerebral cavernous malformations
CCM-1
-
Familial, autosomal dominant
-
-
-
-
-
Carmela Fusco
00165694
0000135714
CCM
CCM-1
Cerebellar hemangiomas, Sovratentorial hemangiomas
Familial
-
-
-
-
-
Carmela Fusco
00170853
0000135715
CCM
CCM-1
Headache (HP:0002076)
Familial
-
-
-
HP:0002076
-
Carmela Fusco
00170854
0000135719
CCM
CCM-1
Headache (HP:0002076), Cerebellar hemangiomas, Sovratentorial hemangiomas
Familial
-
-
-
-
-
Carmela Fusco
00170857
0000138580
CCM
CCM-1
Intracranial haemorrage, fatigable weakness of skeletal (HP:0030197),Cerebellar hemangiomas, bilateral lesion
Familial
-
-
-
-
-
Carmela Fusco
00173726
0000138581
CCM
CCM-1
Headache (HP:0002076)
Familial
-
-
-
-
-
Carmela Fusco
00173727
0000222977
-
-
Cavernous malformation of the optic nerve
Familial, autosomal dominant
30y
30y
30y
-
-
Stefania Battistini
00289359
0000222978
-
Cerebral cavernous malformations
HP:0000951
Familial, autosomal dominant
57y
57y
-
-
-
Stefania Battistini
00289360
0000222979
cerebral cavernous malformations, type 1 (CCM-1)
cerebral cavernous malformations, type 1 (CCM-1)
HP:0001250, HP:0007359
Familial, autosomal dominant
20y
20y
08y
HP:0001250
-
Stefania Battistini
00289361
0000222980
-
-
multiple CCM lesions, but clinically asymptomatic
Familial, autosomal dominant
45y
45y
-
-
-
Stefania Battistini
00289362
0000223051
cerebral cavernous malformations
cerebral cavernous malformations
cutaneous angiomas
Familial, autosomal dominant
47y
47y
46y
-
-
Stefania Battistini
00289443
0000223052
cerebral cavernous malformations
cerebral cavernous malformations
-
Familial, autosomal dominant
55y
39y
39y
-
-
Stefania Battistini
00289444
0000223053
cerebral cavernous malformations
cerebral cavernous malformations
-
Familial, autosomal dominant
55y
52y
-
-
-
Stefania Battistini
00289445
0000223054
cerebral cavernous malformations
cerebral cavernous malformations
-
Familial, autosomal dominant
01y
01y
01y
HP:0002170
-
Stefania Battistini
00289446
0000223055
-
-
-
Familial, autosomal dominant
23y
-
-
-
-
Stefania Battistini
00289447
0000223056
cerebral cavernous malformations
cerebral cavernous malformations
-
Familial, autosomal dominant
29y
22y
-
HP:0001342, HP:0001250
-
Stefania Battistini
00289448
0000223057
cerebral cavernous malformations
cerebral cavernous malformations
-
Unknown
38y
38y
38y
HP:0001342
-
Stefania Battistini
00289449
0000223058
cerebral cavernous malformations
cerebral cavernous malformations
-
Unknown
55y
55y
33y
HP:0001250
-
Stefania Battistini
00289450
0000223078
cerebral cavernous malformations
cerebral cavernous malformations
-
Unknown
33y
09y
09y
HP:0001342, HP:0001250
-
Stefania Battistini
00295507
0000223079
cerebral cavernous malformations
cerebral cavernous malformations
-
Unknown
72y
72y
72y
HP:0001342
-
Stefania Battistini
00295508
0000236354
CCM1
CCM1
-
Unknown
-
-
-
-
-
Carmela Fusco
00311098
0000242111
CCM
CCM1
-
Familial, autosomal dominant
-
-
-
-
-
Carmela Fusco
00320067
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