Global Variome shared LOVD
THOC2 (THO complex 2)
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Phenotypes for disease #00225 (PPHP (pseudopseudohypoparathyroidism (PPHP)), OMIM:612463)
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)
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
Phenotype details
: additional information on the phenotype of the individual, preferably use HPO terms only (http://www.human-phenotype-ontology.org/)
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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Text
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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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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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Date
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all entries after June, 2020
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Date
>=2020-06-15
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
!23
all entries not exactly matching 23
<
Numeric
<23
all entries lower than 23
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Numeric
<=23
all entries lower than, or equal to, 23
>
Numeric
>23
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'
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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21 entries on 1 page. Showing entries 1 - 21.
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Legend
How to query
Phenotype ID
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Phenotype details
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000025575
-
-
Isolated (sporadic)
short stature (HP:0004322); ectopic ossification (HP:0011986);
-
-
-
-
-
Francesca Marta Elli
00029543
0000025578
-
-
Isolated (sporadic)
no short stature (-HP:0004322); brachydactyly (HP:0001156); normal face; normal hormone levels; no intellectual disability (-HP:0001249); no obesity (-HP:0001513); ectopic ossification (HP:0011986); n/a;
18y
18y
-
-
-
Francesca Marta Elli
00029546
0000025606
-
-
Unknown
-
-
-
-
-
-
Guiomar Perez de Nanclares
00029574
0000025642
-
-
Isolated (sporadic)
-
-
-
-
-
-
Susanne Thiele-Schmitz
00029610
0000025655
-
-
Unknown
-
-
-
-
-
-
Susanne Thiele-Schmitz
00029623
0000061342
-
-
Unknown
Height SDS: -0.60; Weight SDS: 1.33; BMI: 14.8; BMI %: 7.3; no short stature (-HP:0004322); no obesity (-HP:0001513);
11y
11y
-
-
-
Arrate Pereda
00081317
0000061352
-
-
Familial, autosomal dominant
Height SDS: -1.61; Weight SDS: -1.13; BMI: 18.8; BMI %: 13.6; no short stature (-HP:0004322); no obesity (-HP:0001513);
14y
14y
-
-
-
Arrate Pereda
00081713
0000061353
-
-
Familial, autosomal dominant
Height SDS: -2.43; Weight SDS: -0.63; BMI: 24.3; BMI %: 73.9; short stature (HP:0004322); no obesity (-HP:0001513);
33y
-
-
-
-
Arrate Pereda
00081713
0000061354
-
-
Familial, autosomal dominant
Height SDS: -2.33; Weight SDS: -0.31; BMI: 26.3; BMI %: 80.8; short stature (HP:0004322); no obesity (-HP:0001513);
42y
-
-
-
-
Arrate Pereda
00081713
0000061355
-
-
Familial, autosomal dominant
Height SDS: -1.98; Weight SDS: 0.84; BMI: 31.0; BMI %: 95.5; short stature (HP:0004322); obesity (HP:0001513);
82y
-
-
-
-
Arrate Pereda
00081713
0000061366
-
-
Unknown
Height SDS: -2.22; Weight SDS: 0.66; BMI: 28.6; BMI %: 90.8; short stature (HP:0004322); no obesity (-HP:0001513);
16y06m
16y06m
-
-
-
Arrate Pereda
00081724
0000078483
-
-
Familial, autosomal dominant
short stature (HP:0004322) (<3rd centile);
-
-
-
-
-
Arrate Pereda
00100255
0000082781
-
-
Unknown
short stature (HP:0004322); brain calcification; round face (HP:0000311); normal hormone levels; no hpercalciuria (-HP:0002150); no intellectual disability (-HP:0001249); hyperphosphatemia; no obesity (-HP:0001513); no ectopic ossification (-HP:0011986);
13y03m
13y03m
-
-
-
Arrate Pereda
00104889
0000083825
-
-
Unknown
mild macrocephaly (PC= 51cm); Broad forehead; Almond shaped eyes; Depressed nasal bridge; midfacial hypoplasia with mandibular prognathia; acromelic limb shortening; Cafe-au-lait spots (left forearm and left scapula); fetal alcohol syndrome history; short stature (HP:0004322); delayed growth (HP:00001510); flat nasal bridge (HP:0005280); normal teeth; brachydactyly-E (HP:0005863); metacapal short; normal hormone levels; no hpercalciuria (-HP:0002150); intellectual disability (HP:0001249); no obesity (-HP:0001513);
16y
18y
06y
6y
-
Arrate Pereda
00105919
0000093339
-
-
Unknown
IUGR; Low birth weight (1600g); supernumerary ribs (13 pairs); hyperactivity; hypoacusia; delayed language acquisition; malar hypoplasia; high-arched palate; thorax asymmetry; pectum excavatum; short stature (HP:0004322); delayed growth (HP:00001510); brachydactyly-E (HP:0005863); broad face; finger short thumb;metacapal short 4rd, metacapal short 5th; thyroid-stimulating hormone excess (HP:0002925); no hpercalciuria (-HP:0002150); mild intellectual disability; no obesity (-HP:0001513);
30y
30y
10y
-
-
Arrate Pereda
00117961
0000104132
-
-
Unknown
Calcinosis (HP:0003761), subcutaneous calcification (HP:0007618), periarticular calcification (HP:0025477), no hypothyroidism (-HP:0000821), no elevated circulating parathyroid hormone level (-HP:0003165); short stature (HP:0004322); round face (HP:0000311); hypercalcemia; hypophosphatemia; normal onset puberty;
-
59y
-
-
-
Nicolas Richard
00131913
0000104136
-
-
Isolated (sporadic)
Subcutaneous calcification (HP:0007618); brachydactyly-E (HP:0005863); no hpercalciuria (-HP:0002150); vitamin D deficiency (HP:0100512)
-
-
-
-
-
Nicolas Richard
00131917
0000116451
-
-
Isolated (sporadic)
short stature (HP:0004322) (<3rd centile); brachydactyly-E (HP:0005863); no calcification; metacapal short 3rd;metacapal short 4rd, metacapal short 5th; normal hormone levels; no hpercalciuria (-HP:0002150); borderline intellectual disability; no obesity (-HP:0001513); no ectopic ossification (-HP:0011986); normal vitamins
17y
17y
-
-
-
Arrate Pereda
00143690
0000117207
-
-
Familial, autosomal dominant
growth delay (HP:0001510); short stature (HP:0004322) (<3rd centile); delayed growth (HP:00001510); no nasal bridge; normal teeth; brachydactyly-E (HP:0005863); normal skin; no calcification; normal face; metacapal short 3rd;metacapal short 4rd, metacapal short 5th; normal hormone levels; no hpercalciuria (-HP:0002150); no intellectual disability (-HP:0001249); decreased body weight (HP:0004325);
11y04m
11y04m
-
growth delay (HP:0001510)
-
Arrate Pereda
00144440
0000117208
-
-
Familial, autosomal dominant
short stature (HP:0004322) (<3rd centile);
-
20y
-
-
-
Arrate Pereda
00144441
0000117209
-
-
Familial, autosomal dominant
short stature (HP:0004322) (<3rd centile);
52y
52y
-
-
-
Arrate Pereda
00144442
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