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Phenotypes for disease #05412 (maculopathy (maculopathy))
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
How to query this table
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space
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all entries beginning with 'p.(Arg'
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combination
Text
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Date
2020
all entries matching the year 2020
|
Date
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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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Date
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Date
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Date
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all entries on or after June 15th, 2020
combination
Date
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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
>
Numeric
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Numeric
>=23
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combination
Numeric
>=20 <30 !23
all entries with values from 20 to 29, but not equal to 23
Some more advanced examples:
Example
Matches
Asian
all entries containing 'Asian', 'asian', including 'Caucasian', 'caucasian', etc.
Asian !Caucasian
all entries containing 'Asian' but not containing 'Caucasian'
Asian|African !Caucasian
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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16 entries on 1 page. Showing entries 1 - 16.
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Legend
How to query
Phenotype ID
Diagnosis/Initial
Diagnosis/Definite
Phenotype details
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000127818
Maculopathy
-
-
Familial, autosomal recessive
-
-
-
-
-
Dror Sharon
00155318
0000127831
Maculopathy
-
-
Familial, autosomal recessive
-
-
-
-
-
Dror Sharon
00155331
0000127833
Maculopathy
-
-
Familial, autosomal recessive
-
-
-
-
-
Dror Sharon
00155333
0000127837
Maculopathy
-
-
Familial, autosomal recessive
-
-
-
-
-
Dror Sharon
00155337
0000127839
Maculopathy
-
-
Familial, autosomal recessive
-
-
-
-
-
Dror Sharon
00155339
0000127845
Maculopathy
-
-
Familial, autosomal recessive
-
-
-
-
-
Dror Sharon
00155345
0000127856
Maculopathy
-
-
Familial, autosomal recessive
-
-
-
-
-
Dror Sharon
00155356
0000127864
Maculopathy
-
-
Familial, autosomal recessive
-
-
-
-
-
Dror Sharon
00155364
0000201911
-
-
Large population study of Age-related Macular Degeneration (AMD) in UK.
Unknown
-
-
-
-
-
Christian Drouet
00264064
0000203540
-
-
Patients presenting with age-related macular degeneration
Unknown
-
-
-
-
-
Christian Drouet
00265753
0000245500
Bilateral, Symmetrical, Cuticular Drusen
-
Fundus: Multiple large, confluent drusen in the central macula and nasal retina Ocular Coherence Tomography (OCT): Numerous confluent drusen in the macula Vision at time of examination was unaffected.
Familial, autosomal recessive
42y
-
-
-
-
Lance P Doucette
00327053
0000245691
-
-
Fundus/History: Bilateral macular schisis, vitreous veils, mild pigmentary retinopathy. Right eye developed shallow rhegmatogenous inferior retinal detachment, and was treated by scleral buckle procedure, cryotherapy with gas injection. Ocular Coherence Tomography: Bilateral parafoveal thinning of the outer retina layers. Central splitting between the inner nuclear and the outer plexiform layer. Electroretinogram (ERG): Small residual cone flicker (6.2 microV in OD, and 7.1 microV in OS) with no measurable responses to ISCE standard seriesd ERG in ffERG
Familial, autosomal recessive
11y
-
-
-
-
Lance P Doucette
00327400
0000245750
-
-
Fundus: No specific findings OCT: Normal ERG:Central loss on multi-focal electroretinogram (abnormal ERG HP:0000512) - Reduced Visual Acuity 20/40 OU (HP:0007663)
Familial, autosomal recessive
15y
-
-
-
-
Lance P Doucette
00327461
0000245752
Retinopathy
-
Fundus findings: Circumscribed central retinal atrophy (Retinal atrophy HP:0001105) Ocular coherence tomography (OCT): Atrophy of outer retina. Bruch's membrane is absent in the central fovea. Electroretinogram: Normal ffERG in the right eye; reduced cone flash and flicker in the left eye (Abnormal ERG HP:0000512)
Familial, autosomal recessive
29y
-
-
-
-
Lance P Doucette
00327463
0000300515
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Oscar F Chacon-Camacho
00408394
0000308985
maculopathy
-
see paper
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00417503
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