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Phenotypes for disease #04187 (POF (ovarian failure, premature (POF)))
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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combination
Text
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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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Date
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Date
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Date
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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
23|24
all entries exactly matching 23 or 24
!
Numeric
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all entries not exactly matching 23
<
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:
Example
Matches
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all entries containing 'Asian', 'asian', including 'Caucasian', 'caucasian', etc.
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all entries containing 'South Asian', but not containing 'South East Asian'
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22 entries on 1 page. Showing entries 1 - 22.
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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
0000053385
secondary amenorrhea (HP:0000869), FSH=124 IU/L
-
-
Unknown
-
-
-
-
-
Lin Li
00073649
0000053394
-
-
-
Unknown
-
-
-
-
-
Lin Li
00073650
0000053395
-
-
-
Unknown
-
-
-
-
-
Lin Li
00073651
0000079483
. The serum FSH level of the patient who carried DelG mutation was 51.07 IU/l; LH = 27.69 IU/l; E2 (estradiol) = 82.64 pmol/l; testosterone (T) = 1.94 nmol/l; prolactin = 15.85 ng/ml.
-
-
Unknown
-
-
-
-
-
Lin Li
00101241
0000199419
see paper; ...
non-syndromic primary ovarian insufficiency
POF-15
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00260885
0000203626
Premature ovarian failure
-
-
Familial, autosomal recessive
-
-
-
-
-
Alice Fiévet
00265841
0000207661
primary amenorrhea, premature ovarian failure
Primary amenorrhea
premature ovarian failure
Unknown
16y
16y
16y
-
-
Yajuan Yang
00269785
0000207662
13y-menarche, since then suffered from oligomenorrhea; 16y-amenorrhea
secondary amenorrhea
premature ovarian failure
Unknown
16y
16y
16y
16y
-
Yajuan Yang
00269783
0000242708
primary amenorrhea and delayed puberty
hypergonadotropic hypogonadism
premature ovarian insufficiency
Familial, autosomal recessive
32y
17y
-
17y
-
Asma Sassi
00324127
0000242711
primary amenorrhea and delayed puberty
hypergonadotropic hypogonadism
premature ovarian insufficiency
Familial, autosomal recessive
32y
17y
-
17y
-
Asma Sassi
00324129
0000250700
see paper; ...
premature ovarian insufficiency
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00332516
0000250701
see paper; ...
premature ovarian insufficiency
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00332517
0000295855
see paper; ...
premature ovarian failure
POF9
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00403108
0000295856
see paper; ...
premature ovarian failure
POF9
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00403109
0000295861
see paper; ..., primary amenorrhea, hypothyroidism, hypergonadotropic hypogonadism
ovarian failure
POF10
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00403114
0000295863
see paper; ..., delayed puberty, primary amenorrhoea, hypergonadotrophic hypogonadism, absence of ovaries, small uterus
premature ovarian failure
POF10
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00403116
0000300319
-
Diminished ovarian reserve (DOR)
POF
Familial, autosomal recessive
29y
31y
-
oligomenorrhea (HP:0000876); Female infertility (HP:0008222)
-
Maeve Soen
00408189
0000302346
see paper; ..., y-amenorrhea (HP:0000141), no pregnancies
-
POF
Familial, autosomal recessive
35y
34y
34y
see paper; ..., oligomenorrhea (HP:0000876); premature ovarian insufficiency; (HP:0008209); aplasia/hypoplasia of the uterus (HP:0008684)
-
Maeve Soen
00409231
0000303161
see paper; ..., 23y-amenorrhea, no pregnancies
-
-
Unknown
29y
-
-
-
-
Johan den Dunnen
00411071
0000321906
see paper; ..., primary amenorrhea, 13y-puberty, normal development secondary sex characteristics
premature ovarian failure
-
Familial, autosomal recessive
19y
-
-
-
-
Johan den Dunnen
00431306
0000321911
see paper; ..., primary amenorrhea, normal female secondary sexual characteristics, heigh 163 cm, weight 51 kg; high serum gonadotropin concentrations
primary amenorrhea
ODG1
Familial, autosomal recessive
17y
-
-
-
-
Johan den Dunnen
00431311
0000346440
see paper; ..., 15y-menarche, irregular menstrual cycles, ovaries atrophic, no visible follicle
premature ovarian failure
POF25
Familial, autosomal recessive
20y
-
-
-
-
Johan den Dunnen
00457990
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