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Phenotypes for disease #06887 (dysplasia, bone (dysplasia, bone))
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
How to query this table
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Column type
Example
Matches
Text
Arg
all entries containing 'Arg'
space
Text
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Text
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Text
!fs
all entries not containing 'fs'
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Text
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all entries beginning with 'p.(Arg'
$
Text
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all entries ending with 'Ser)'
=""
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Text
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all entries exactly matching 'p.0'
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Text
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combination
Text
*|Ter !fs
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Date
2020
all entries matching the year 2020
|
Date
2020-03|2020-04
all entries matching March or April, 2020
!
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
<=2020-06
all entries in or before June, 2020
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Date
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all entries after June, 2020
>=
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
<=
Numeric
<=23
all entries lower than, or equal to, 23
>
Numeric
>23
all entries higher than 23
>=
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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36 entries on 1 page. Showing entries 1 - 36.
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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
Owner
Individual ID
0000290718
hypophosphatemic rickets
XLHR
see paper; ...
Isolated (sporadic)
1y4m
-
-
-
Johan den Dunnen
00397594
0000290719
hypophosphatemic rickets
XLHR
see paper; ...
Isolated (sporadic)
6y
-
-
-
Johan den Dunnen
00397595
0000290720
hypophosphatemic rickets
XLHR
see paper; ...
Isolated (sporadic)
2y6m
-
-
-
Johan den Dunnen
00397596
0000290721
hypophosphatemic rickets
XLHR
see paper; ...
Familial, X-linked
1y
-
-
-
Johan den Dunnen
00397597
0000290722
hypophosphatemic rickets
XLHR
see paper; ...
Isolated (sporadic)
10m
-
-
-
Johan den Dunnen
00397598
0000290723
hypophosphatemic rickets
XLHR
see paper; ...
Familial, X-linked
1y
-
-
-
Johan den Dunnen
00397599
0000290724
hypophosphatemic rickets
XLHR
see paper; ...
Familial, X-linked
5y7m
-
-
-
Johan den Dunnen
00397600
0000290725
hypophosphatemic rickets
XLHR
see paper; ...
Isolated (sporadic)
1y
-
-
-
Johan den Dunnen
00397601
0000290726
hypophosphatemic rickets
XLHR
see paper; ...
Isolated (sporadic)
2y
-
-
-
Johan den Dunnen
00397602
0000290727
multiple epiphyseal dysplasia
EDM1
see paper; ...
Isolated (sporadic)
7y
-
-
-
Johan den Dunnen
00397603
0000290728
pseudoachondroplasia
PSACH
see paper; ...
Isolated (sporadic)
5y7m
-
-
-
Johan den Dunnen
00397604
0000290729
pseudoachondroplasia
PSACH
see paper; ...
Isolated (sporadic)
5y7m
-
-
-
Johan den Dunnen
00397605
0000290730
pseudoachondroplasia
PSACH
see paper; ...
Isolated (sporadic)
4y10m
-
-
-
Johan den Dunnen
00397606
0000290731
pseudoachondroplasia
PSACH
see paper; ...
Isolated (sporadic)
2y3m
-
-
-
Johan den Dunnen
00397607
0000290732
pseudoachondroplasia
PSACH
see paper; ...
Isolated (sporadic)
2y6m
-
-
-
Johan den Dunnen
00397608
0000290733
pseudoachondroplasia
PSACH
see paper; ...
Isolated (sporadic)
2y
-
-
-
Johan den Dunnen
00397609
0000290734
pseudoachondroplasia
PSACH
see paper; ...
Isolated (sporadic)
3y
-
-
-
Johan den Dunnen
00397610
0000290735
spondylometaphyseal dysplasia, Kozlowski type
SMDK
see paper; ...
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00397611
0000290736
metatropic dysplasia
MTD
see paper; ...
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00397612
0000290737
spondylometaphyseal dysplasia, Kozlowski type
SMDK
see paper; ...
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00397613
0000290738
spondylometaphyseal dysplasia, Kozlowski type
SMDK
see paper; ...
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00397614
0000290739
multiple epiphyseal dysplasia
EDM5
see paper; ...
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00397615
0000290740
Stickler syndrome
STL2
see paper; ...
Familial, autosomal dominant
-
-
-
-
Johan den Dunnen
00397616
0000290741
spondyloepiphyseal dysplasia tarda
SEDT
see paper; ...
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00397617
0000290742
chondrodysplasia punctata
CDPX1
see paper; ...
Familial, X-linked recessive
-
-
-
-
Johan den Dunnen
00397618
0000290743
trichorhinophalangeal syndrome
TRPS
see paper; ...
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00397619
0000290744
Schimke immunoosseous dysplasia
SIOD
see paper; ...
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00397620
0000290745
hypophosphataemic rickets
ARHR2
see paper; ...
Familial, autosomal recessive
-
-
-
-
Johan den Dunnen
00397621
0000290746
geleophysic dysplasia
GPHYSD2
see paper; ...
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00397622
0000290747
geleophysic dysplasia
GPHYSD2
see paper; ...
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00397623
0000290748
acromicric dysplasia
ACMICD
see paper; ...
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00397624
0000290749
Weill-Marchesani syndrome
WMS2
see paper; ...
Isolated (sporadic)
-
-
-
-
Johan den Dunnen
00397625
0000299775
kyphomelic dysplasia
-
see paper; ..., no intellectual disability; no developmental delay; no neurological symptoms; conductive hearing impairment, hyperopia; respiratory disorders in neonatal period; joint contracture knee/hip; talipes equinovarus; respiratory disorders in neonatal period; bitemporal constriction; arched eyebrows; hypertelorism; proptosis; ptosis; low-set, large ears; midface hypoplasia; depressed nasal bridge, upturned nares, thick nasal alae; tented upper lip; micrognathia; small mouth with thin upper lip; cleft palate; intermittent esotopia; no brachycephaly; narrow thorax; hooked clavicles; short, wavy ribs; anteriorly cupped ribs; no platyspondyly; no kyphoscoliosis; no large pedicles; iliac flaring; horizontal acetabular roof; limbs humeral bowing, radial bowing, no ulnar bowing, femoral bowing, tibial bowing, no fibular bowing, no bone spur, metaphyseal broadening, no pterygia, no stippled epiphysis, fracture; relatively long hands and feet; no short metacarpals; postnatal osteoporosis
Isolated (sporadic)
-
-
-
-
Toshiyuki Itai
00398645
0000299776
kyphomelic dysplasia
-
see paper; ..., no intellectual disability; no developmental delay; febrile seizures, epilepsy; velopharyngeal insufficiency, astigmatism; respiratory disorders in neonatal period; no joint contracture; talipes equinovarus; respiratory disorders in neonatal period; no bitemporal constriction; arched eyebrows; hypertelorism; proptosis; ptosis; low-set, large ears; midface hypoplasia; depressed nasal bridge, upturned nares, thick nasal alae; tented upper lip; no micrognathia; no small mouth with thin upper lip; no cleft palate; no intermittent esotopia; narrow thorax; no hooked clavicles; no short, wavy ribs; no anteriorly cupped ribs; no platyspondyly; kyphoscoliosis; no large pedicles; iliac flaring; no horizontal acetabular roof; limbs humeral bowing, no radial bowing, no ulnar bowing, femoral bowing, tibial bowing, no fibular bowing, no bone spur, metaphyseal broadening, no pterygia, no stippled epiphysis, no fracture; relatively long hands and feet; no short metacarpals; no postnatal osteoporosis
Isolated (sporadic)
-
-
-
-
Toshiyuki Itai
00398646
0000299777
kyphomelic dysplasia
-
see paper; ..., intellectual disability; developmental delay; optic nerve hypoplasia; glossoptosis; respiratory disorders in neonatal period; no joint contracture; no talipes equinovarus; respiratory disorders in neonatal period; bitemporal constriction; arched eyebrows; hypertelorism; proptosis; ptosis; low-set, large ears; midface hypoplasia; depressed nasal bridge, upturned nares, thick nasal alae; tented upper lip; micrognathia; small mouth with thin upper lip; no cleft palate; intermittent esotopia; brachycephaly; narrow thorax; hooked clavicles; short, wavy ribs; anteriorly cupped ribs; platyspondyly; no kyphoscoliosis; large pedicles; iliac flaring; horizontal acetabular roof; limbs humeral bowing, radial bowing, no ulnar bowing, femoral bowing, tibial bowing, no fibular bowing, bone spur, metaphyseal broadening, no pterygia, stippled epiphysis, fracture; relatively long hands and feet; no short metacarpals; postnatal osteoporosis
Isolated (sporadic)
-
-
-
-
Toshiyuki Itai
00398647
0000299778
Kyphomelic dysplasia
-
see paper; ..., intellectual disability; developmental delay; optic nerve hypoplasia; tracheomalacia; respiratory disorders in neonatal period; no joint contracture; talipes equinovarus; respiratory disorders in neonatal period; bitemporal constriction; arched eyebrows; hypertelorism; proptosis; ptosis; low-set, large ears; midface hypoplasia; depressed nasal bridge, upturned nares, thick nasal alae; tented upper lip; micrognathia; small mouth with thin upper lip; no cleft palate; intermittent esotopia; brachycephaly; narrow thorax; hooked clavicles; short, wavy ribs; no anteriorly cupped ribs; platyspondyly; no kyphoscoliosis; no large pedicles; iliac flaring; horizontal acetabular roof; limbs humeral bowing, radial bowing, no ulnar bowing, femoral bowing, tibial bowing, fibular bowing, no bone spur, metaphyseal broadening, no pterygia, no stippled epiphysis, no fracture; relatively long hands and feet; no short metacarpals; postnatal osteoporosis
Isolated (sporadic)
-
-
-
-
Toshiyuki Itai
00398648
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