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Phenotypes for disease #05301 (ROP (retinopathy of prematurity (ROP)))
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/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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all entries ending with 'Ser)'
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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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all entries in or before June, 2020
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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
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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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all entries higher than 23
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Numeric
>=23
all entries higher than, or equal to, 23
combination
Numeric
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all entries with values from 20 to 29, but not equal to 23
Some more advanced examples:
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Matches
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all entries containing 'Asian', 'asian', including 'Caucasian', 'caucasian', etc.
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all entries containing 'Asian' but not containing 'Caucasian'
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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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26 entries on 1 page. Showing entries 1 - 26.
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Legend
How to query
Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000084378
retinopathy of prematurity (ROP)
-
-
Familial, autosomal dominant
-
-
-
-
Johan den Dunnen
00106573
0000084386
retinopathy of prematurity (ROP)
-
-
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00106581
0000209398
Stage 2 retinopathy of prematurity (HP:0500051), mild hypermetropia at 01y06m (HP:0031728), born 25 weeks gestation, 950g, 3 months oxygen therapy, spontaneous regression
Retinopathy of prematurity
-
Familial, X-linked
01y06m
-
-
-
Jasmine Chen
00274458
0000210097
-
Retinopathy of Prematurity
Retinopathy of Prematurity
Familial, autosomal dominant
?
?
-
-
Dimitra Ilektra Lerou
00275472
0000308486
no hearing impairment
-
retinopathy of prematurity
Familial, X-linked
-
5m
-
-
LOVD
00416975
0000308781
highest stage of disease: 5; multiple comorbidities and poor health
-
aggressive posterior retinopathy of prematurity
Familial, autosomal dominant
-
-
-
-
LOVD
00417266
0000308782
asymptomatic twin, had an uneventful course with no systemic maladies
-
aggressive posterior retinopathy of prematurity
Familial, autosomal dominant
-
-
-
-
LOVD
00417267
0000308783
-
-
aggressive posterior retinopathy of prematurity
Familial, autosomal dominant
-
-
-
-
LOVD
00417268
0000308784
highest stage of disease: 5; sole surviving triplet
-
aggressive posterior retinopathy of prematurity
Familial, autosomal dominant
-
-
-
-
LOVD
00417269
0000308785
fluorescein angiography: peripheral avascular zone can be appreciated
-
aggressive posterior retinopathy of prematurity
Familial, autosomal dominant
-
-
-
-
LOVD
00417270
0000308786
highest stage of disease: 4b
-
retinopathy of prematurity
Familial, autosomal dominant
-
-
-
-
LOVD
00417271
0000308787
highest stage of disease: 1
-
retinopathy of prematurity
Familial, autosomal dominant
-
-
-
-
LOVD
00417272
0000308788
born at 28 weeks of gestational age, birth weight of 880 grams; required laser treatment for threshold retinopathy of prematurity at 92 days of life; required only one laser treatment to each eye and the retinopathy of prematurity regressed rapidly with no cicatricial sequela
-
retinopathy of prematurity
Familial, autosomal dominant
-
-
-
-
LOVD
00417273
0000308789
born at 26 weeks of gestational age, birth weight of 780 grams; treated for threshold retinopathy of prematurity at 78d of life; required only one laser treatment to each eye and the retinopathy of prematurity regressed with no cicatricial sequela
-
retinopathy of prematurity
Familial, autosomal dominant
-
-
-
-
LOVD
00417274
0000308790
born at 24 weeks of gestational age, birth weight of 650 grams; required initial retinal laser surgery to each eye at 68 days of life and then required a second laser treatment to both eyes for progression of neovascular retinopathy of prematurity; mild cicatricial changes from the retinopathy of prematurity, such as mild straightening of temporal arcade vessels and high myopia (-9.00 diopters in both eyes); twin brother bearing no mutation; required two laser treatments as opposed to her brother who only required one treatment
-
retinopathy of prematurity
Familial, autosomal dominant
-
-
-
-
LOVD
00417275
0000308858
-
-
retinopathy of prematurity
Isolated (sporadic)
-
-
-
-
LOVD
00417371
0000308871
-
-
retinopathy of prematurity
Isolated (sporadic)
-
-
-
-
LOVD
00417384
0000308872
-
-
retinopathy of prematurity
Isolated (sporadic)
-
-
-
-
LOVD
00417385
0000308873
-
-
retinopathy of prematurity
Isolated (sporadic)
-
-
-
-
LOVD
00417386
0000308874
-
-
retinopathy of prematurity
Isolated (sporadic)
-
-
-
-
LOVD
00417387
0000308875
-
-
retinopathy of prematurity
Isolated (sporadic)
-
-
-
-
LOVD
00417388
0000308876
-
-
retinopathy of prematurity
Isolated (sporadic)
-
-
-
-
LOVD
00417389
0000308877
-
-
retinopathy of prematurity
Isolated (sporadic)
-
-
-
-
LOVD
00417390
0000308882
-
-
retinopathy of prematurity
Isolated (sporadic)
-
-
-
-
LOVD
00417395
0000308883
-
-
retinopathy of prematurity
Isolated (sporadic)
-
-
-
-
LOVD
00417396
0000308884
-
-
retinopathy of prematurity
Isolated (sporadic)
-
-
-
-
LOVD
00417397
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