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Phenotypes for disease #05195 (HCINF2 (hypercalcemia, infantile, type 2 (HCINF-2)), OMIM:616963)
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
How to query this table
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Text
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space
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Text
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all entries beginning with 'p.(Arg'
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Text
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Date
2020
all entries matching the year 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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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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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
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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
>=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'
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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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17 entries on 1 page. Showing entries 1 - 17.
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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
0000073558
diagnosis infantile hypercalcemia; ephrocalcinosis (HP:0000121), Hypercalciuria (HP:0002150), Hypercalcemia (HP:0003072), Hypophosphatemia (HP:0002148), Hypoparathyroidism (HP:0000829), Increased serum 1,25-dihydroxyvitamin D3 (HP:0003152)
-
-
Familial, autosomal recessive
00y02m
-
-
-
-
Pieter Klap
00074404
0000073559
diagnosis infantile hypercalcemia; failure to thrive (HP:0001508), Polyuria (HP:0000103), Dehydration (HP:0001944), no muscular hypotonia (-HP:0001252), Nephrocalcinosis (HP:0000121), Hypercalciuria (HP:0002150), Hypercalcemia (HP:0003072), Hypophosphatemia (HP:0002148)
-
-
Familial, autosomal recessive
00y02m
-
-
-
-
Johan den Dunnen
00074405
0000073560
Failure to thrive (HP:0001508), Polyuria (HP:0000103), Dehydration (HP:0001944), Muscular hypotonia (HP:0001252), Nephrocalcinosis (HP:0000121), Hypercalciuria (HP:0002150), Hypercalcemia (HP:0003072), Hypophosphatemia (HP:0002148), Hypoparathyroidism (HP:0000829), Increased serum 1,25-dihydroxyvitamin D3 (HP:0003152),
-
-
Familial, autosomal recessive
<00y01m
-
<00y01m
failure to thrive (HP:0001508)
-
Pieter Klap
00074402
0000073561
failure to thrive (HP:0001508), Polyuria (HP:0000103), Dehydration (HP:0001944), no muscular hypotonia (-HP:0001252), Nephrocalcinosis (HP:0000121), Hypercalciuria (HP:0002150), Hypercalcemia (HP:0003072), Hypophosphatemia (HP:0002148)
-
-
Familial, autosomal recessive
00y01m
-
00y01m
failure to thrive (HP:0001508)
-
Pieter Klap
00074403
0000073562
see paper; …
-
-
Familial, autosomal recessive
14y
-
2m
-
-
Johan den Dunnen
00095161
0000073563
see paper; …
-
-
Unknown
10y
-
4m
-
-
Johan den Dunnen
00095162
0000073564
see paper; …
-
-
Unknown
17y
-
9m
-
-
Johan den Dunnen
00095163
0000073565
see paper; …
-
-
Familial, autosomal recessive
3y
-
10m
-
-
Johan den Dunnen
00095164
0000073566
see paper; …
-
-
Familial, autosomal recessive
3y
-
1m
-
-
Johan den Dunnen
00095165
0000073567
see paper; …
-
-
Familial, autosomal recessive
11m
-
3m
-
-
Johan den Dunnen
00095166
0000073568
see paper; …
-
-
Familial, autosomal recessive
1y
-
3m
-
-
Johan den Dunnen
00095167
0000073569
see paper; …
-
-
Familial, autosomal recessive
11m
-
4m
-
-
Johan den Dunnen
00095168
0000073570
see paper; …
-
-
Familial, autosomal recessive
11y
-
7m
-
-
Johan den Dunnen
00095169
0000073571
see paper; …
-
-
Unknown
6y
-
6m
-
-
Johan den Dunnen
00095170
0000073572
see paper; …
-
-
Familial, autosomal recessive
1y
-
3m
-
-
Johan den Dunnen
00095171
0000073573
see paper; …
-
-
Familial, autosomal recessive
3y6m
-
1y6m
-
-
Johan den Dunnen
00095172
0000187182
Nephrocalcinosis, Muscular hypotonia, Failure to thrive
-
-
Familial, autosomal recessive
-
-
-
-
-
Valeriia Apukhtina
00248174
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