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Phenotypes for disease #03686 (ACRDYS2 (acrodysostosis, with/without hormone resistance, type 2), OMIM:614613)
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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Operator
Column type
Example
Matches
Text
Arg
all entries containing 'Arg'
space
Text
Arg Ser
all entries containing 'Arg' and 'Ser'
|
Text
Arg|Ser
all entries containing 'Arg' or 'Ser'
!
Text
!fs
all entries not containing 'fs'
^
Text
^p.(Arg
all entries beginning with 'p.(Arg'
$
Text
Ser)$
all entries ending with 'Ser)'
=""
Text
=""
all entries with this field empty
=""
Text
="p.0"
all entries exactly matching 'p.0'
!=""
Text
!=""
all entries with this field not empty
!=""
Text
!="p.0"
all entries not exactly matching 'p.0?'
combination
Text
*|Ter !fs
all entries containing '*' or 'Ter' but not containing 'fs'
Date
2020
all entries matching the year 2020
|
Date
2020-03|2020-04
all entries matching March or April, 2020
!
Date
!2020-03
all entries not matching March, 2020
<
Date
<2020
all entries before the year 2020
<=
Date
<=2020-06
all entries in or before June, 2020
>
Date
>2020-06
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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31 entries on 1 page. Showing entries 1 - 31.
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Legend
How to query
Phenotype ID
Phenotype details
Diagnosis/Initial
Diagnosis/Definite
Inheritance
Age/Examination
Age/Diagnosis
Age/Onset
Phenotype/Onset
Protein
Owner
Individual ID
0000050888
advanced bone age; nasal hypoplasia; depressed nasal bridge; prominent mandible; severe brachydactyly; short metatarsals, metacarpals, and phalanges; cone-shaped epiphyses; speech delay, psychomotoer delay (walked at 17m of age); intracranial hypertension with thrombophlebitis of the transverse sinus and jugular
-
-
Familial, autosomal dominant
4y
-
-
-
-
Johan den Dunnen
00064690
0000050889
intrauterine growth retardation; advanced bone age; nasal hypoplasia; depressed nasal bridge; severe brachydactyly; short metatarsals, metacarpals, and phalanges; cone-shaped epiphyses; speech delay requiring orthophony, fine-motor-skill impairment; intracranial hypertension with jugular stenosis requiring derivation
-
-
Familial, autosomal dominant
7y
-
-
-
-
Johan den Dunnen
00064691
0000050890
-
-
-
Isolated (sporadic)
-
-
-
-
-
Danielle Lynch
00064692
0000050891
advanced bone age; nasal hypoplasia; depressed nasal bridge; severe brachydactyly; short metatarsals, metacarpals, and phalanges; cone-shaped epiphyses; speech delay requiring orthophony, fine-motor-skill impairment
-
-
Familial, autosomal dominant
4y
-
-
-
-
Johan den Dunnen
00064693
0000050892
small hands, midface hypoplasia
-
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00064694
0000050893
-
-
-
Isolated (sporadic)
-
-
-
-
-
Danielle Lynch
00064695
0000050895
-
-
-
Isolated (sporadic)
-
-
-
-
-
Danielle Lynch
00064697
0000050896
advanced bone age; nasal hypoplasia; depressed nasal bridge; severe brachydactyly; short metatarsals, metacarpals, and phalanges; cone-shaped epiphyses; speech delay, psychomotor delay requiring physiotherapy
-
-
Familial, autosomal dominant
3y
-
-
-
-
Johan den Dunnen
00064698
0000050897
mild short stature, small hands, midface hypoplasia, lumbar stenosis; significant developmental disability; cryptorchidism
-
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00064699
0000050898
mild short stature, small hands, midface hypoplasia, lumbar stenosis; mild developmental disability; congenital hypothyroidism
-
-
Familial, autosomal dominant
-
-
-
-
-
Johan den Dunnen
00064700
0000060303
PTH resistance, TSH resistance, obesity, mental retardation, craniosynostosis
-
-
Familial, autosomal dominant
-
07y
-
-
-
Francesca Marta Elli
00080728
0000060305
TSH resistance, short stature, obesity, brachydactily, mental rtardation cholelithiasis
-
-
Unknown
-
47y
-
-
-
Francesca Marta Elli
00080729
0000060306
short stature, obesity, dysmorphic facies, brachydactily, mental retardation
-
-
Familial, autosomal dominant
-
04y
-
-
-
Francesca Marta Elli
00080730
0000060307
short stature, obesity, dysmorphic facies, brachydactily, mental retardation, cryptorchidism, vesicoureteral reflux
-
-
-
-
29y
-
-
-
Francesca Marta Elli
00080732
0000060317
PTH resistance, dysmorphic facies, btachydactily, shypo-deformity of knees
-
-
Unknown
-
03y
-
-
-
Francesca Marta Elli
00080740
0000060318
short stature, dysmorphic facies, brachydactily, mental retardation, shypo-deformity of knees and shoulders
-
-
Unknown
-
15y
-
-
-
Francesca Marta Elli
00080741
0000060338
dysmorphic facies, brachydactily, mental retardation, failure to thrive, shypo-deformity of knees and shoulders
-
-
Unknown
-
0,9y
-
-
-
Francesca Marta Elli
00080759
0000060339
transient PTH resistance, short stature, dysmorphic facies, brachydactily, mental retardation, recurrent otitis media, cryptorchidism
-
-
Unknown
-
3.5y
-
-
-
Francesca Marta Elli
00080760
0000060340
PTH resistance, short stature, obesity, dysmorphic facies, brachydactily, mental retardation, DMT1, recurrent otitis media, lack of puberal growth spurt
-
-
-
-
14.7y
-
-
-
Francesca Marta Elli
00080761
0000060341
PTH resistance, short stature, dysmorphic facies, brachydactily, mental retardation, recurrent otitis media, hypertension, aortic valve insufficiency
-
-
-
-
12.5y
-
-
-
Francesca Marta Elli
00080762
0000060342
PTH resistance, short stature, obesity, dysmorphic facies, btachydactily, mental retardation, recurrent otitis media
-
-
-
-
07y
-
-
-
Francesca Marta Elli
00080764
0000060343
short stature, obesity, dysmorphic facies, brachydactily, mental retardation, recurrent otitis media, unilateral hydronephrosis
-
-
-
-
3.5y
-
-
-
Francesca Marta Elli
00080765
0000060344
short stature, obesity, dysmorphic facies, brachydactily, mental retardation, cone-shaped epiphyses, advanced bone age
-
-
-
-
14y
-
-
-
Francesca Marta Elli
00080766
0000060345
obesity, dysmorphic facies, brachydatily, mental retardation, cone-shaped epiphyses, advanced bone age
-
-
-
-
07y
-
-
-
Francesca Marta Elli
00080767
0000060346
borderline PTH resistance, short stature, dysmorphic facies, brachydactily, mental retardation, advanced bone age
-
-
Familial, autosomal dominant
-
39y&37y
-
-
-
Francesca Marta Elli
00080769
0000060347
short stature, dysmorphic facies, brachydactily, mental retardation, advancd bone age
-
-
-
-
10.5y
-
-
-
Francesca Marta Elli
00080770
0000060348
dysmorphic facies, brachydactily, mental retardation, advanced bone age
-
-
-
-
8.5y
-
-
-
Francesca Marta Elli
00080771
0000060349
short stature, dysmorphic facies, brachydactily, mental retardation, advanced bone age
-
-
-
-
17y
-
-
-
Francesca Marta Elli
00080772
0000060350
short stature, dysmorphic facies, brachydactily, mental retardation, advanced bone age
-
-
Familial, autosomal dominant
-
17y&4.11y
-
-
-
Francesca Marta Elli
00080773
0000104163
severe brachydactyly; thick hair; hypertrichosis arms; hip bone replacement–osteoarthrosis; abnormal stature, normal teeth; mil/moderate intellectual disability; dysmorphic face; no clacifications; normal calcium homeastasis; high circulating parathyroid hormone (HP:0003165); vitamin D deficiency (HP:0100512)
-
-
Unknown
35y
35y
-
-
-
Arrate Pereda
00131945
0000239605
neurodevelopmental abnormality, global developmental delay, short stature, facial abnormality; delayed growth; progressive intellectual disability (HP:0006887); dysmorphic face (HP:0001999); decreased body weight (HP:0004325)
1
-
Unknown
-
-
-
-
-
Andreas Laner
00315859
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