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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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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|
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
|
0000126069 |
Arthrogryposis multiplex congenita |
prenatal |
- |
Unknown |
- |
- |
- |
prenatal |
- |
Andreas Laner |
00153391 |
0000164891 |
- |
cardiac conduction defect |
- |
Unknown |
- |
- |
- |
- |
- |
Soma Das |
00216439 |
0000164991 |
LV hypertrophy, arrhythmia, distal weakness ; CPK elevated (HP:0003236) |
cardiac conduction defect |
- |
Unknown |
- |
- |
- |
- |
- |
Tom Winder |
00216539 |
0000165009 |
deceased; CPK 12 |
cardiac conduction defect |
- |
Familial |
- |
- |
40y |
- |
- |
Johan den Dunnen |
00216557 |
0000165013 |
no peripheral neuropathy; 45y-lipodystrophy, lack ofsubcutaneous fat tissue; no diabetes; deceased; CPK 83-111 |
cardiac conduction defect |
- |
Familial |
- |
- |
23y |
- |
- |
Johan den Dunnen |
00216561 |
0000165014 |
no peripheral neuropathy; adolescence lipodystrophy, generalized reduction subcutaneous fat tissue; no diabetes |
cardiac conduction defect |
- |
Familial |
- |
- |
22y |
- |
- |
Johan den Dunnen |
00216562 |
0000165017 |
no muscle weakness; biatrial enlargement; no contractures; MRI muscle abnormalities mild to severe |
cardiac conduction defect |
- |
Familial |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216565 |
0000165019 |
no muscle weakness; biatrial enlargement; no contractures; MRI muscle abnormalities mild to severe |
cardiac conduction defect |
- |
Familial |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216567 |
0000165020 |
no muscle weakness; left atrium dilation; no contractures; MRI muscle abnormalities mild to modeate |
cardiac conduction defect |
- |
Familial |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216568 |
0000165021 |
no muscle weakness; no contractures; MRI muscle abnormalities absent to mild |
cardiac conduction defect |
- |
Familial |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216569 |
0000165022 |
no muscle weakness; no contractures; MRI muscle abnormalities mild to modeate |
cardiac conduction defect |
- |
Familial |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216570 |
0000165026 |
no muscle weakness; no contractures; MRI muscle abnormalities moderate to absent |
cardiac conduction defect |
- |
Familial |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216574 |
0000165029 |
no muscle weakness; no contractures; MRI muscle abnormalities absent to mild |
cardiac conduction defect |
- |
Familial |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216577 |
0000165030 |
no muscle weakness; no contractures; MRI muscle abnormalities absent to modeate |
cardiac conduction defect |
- |
Familial |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216578 |
0000165031 |
no muscle weakness; no contractures; MRI muscle abnormalities absent to mild |
cardiac conduction defect |
- |
Familial |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216579 |
0000165033 |
no muscle weakness; no contractures |
cardiac conduction defect |
- |
Familial |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216581 |
0000165146 |
- |
cardiac conduction disease (CCD) |
- |
Familial |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216694 |
0000204428 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Liliana Dain |
00266692 |
0000204505 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Liliana Dain |
00266735 |
0000204506 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Liliana Dain |
00266736 |
0000204545 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Liliana Dain |
00266748 |
0000204594 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Liliana Dain |
00266777 |
0000204925 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Liliana Dain |
00267001 |
0000351393 |
see paper; ..., palpitations; no cardiac arrest; sinus pauses (3 s); AV conduction disease second atrioventricular block (type 1); atrial fibrillation, flutter; monomorphic non-sustained ventricular tachycardia, premature ventricular contractions; hypertrophic cardiomyopathy; cardiac MRI septal hypertrophy (23 mm); no myocarditis |
cardiac conduction defect |
- |
Familial, autosomal recessive |
- |
- |
11y-15y |
palpitations |
- |
Johan den Dunnen |
00466008 |
0000351394 |
see paper; ..., palpitations; sinus bradycardia; AV conduction disease PQ time of 200 ms second atrioventricular block; no atrial arrhythmia; no ventricular arrhythmia; hypertrophic cardiomyopathy; cardiac MRI septal hypertrophy (16mm); no myocarditis |
cardiac conduction defect |
- |
Familial, autosomal recessive |
- |
- |
21y-25y |
palpitations |
- |
Johan den Dunnen |
00466009 |
0000351395 |
see paper; ..., no cardiac arrest; no sinus node disease; first and second atrioventricular block (type 1 and 2:1); atrial fibrillation, flutter; monomorphic non-sustained ventricular tachycardia; no hypertrophic cardiomyopathy; no myocarditis |
cardiac conduction defect |
- |
Familial, autosomal recessive |
- |
- |
21y-25y |
- |
- |
Johan den Dunnen |
00466010 |
0000351396 |
see paper; ..., no cardiac arrest; SA-block sinus pauses (5s); AV conduction disease first atrioventricular block; no atrial arrhythmia; no ventricular arrhythmia; no hypertrophic cardiomyopathy; no myocarditis |
cardiac conduction defect |
- |
Familial, autosomal recessive |
- |
- |
21y-25y |
- |
- |
Johan den Dunnen |
00466011 |
0000351397 |
see paper; ..., cardiac arrest; cardiac arrest following bradycardia; SA block sinus arrest; AV conduction disease first and second atrioventricular block (type 1); episodes of high atrial rate; monomorphic non-sustained ventricular tachycardia; no hypertrophic cardiomyopathy; cardiac MRI possible myocarditis; possible myocarditis |
cardiac conduction defect |
- |
Familial, autosomal recessive |
- |
- |
16y-20y |
cardiac arrest |
- |
Johan den Dunnen |
00466012 |
0000351398 |
see paper; ..., chest pain; cardiac arrest following bradycardia; no sinus node disease; AV conduction disease first atrioventricular block; no atrial arrhythmia; ventricular tachycardia; no hypertrophic cardiomyopathy; cardiac MRI significant LV fibrosis, inflammation; clinical myocarditis (not on cardiac histology) |
cardiac conduction defect |
- |
Familial, autosomal recessive |
- |
- |
11y-15y |
chest pain |
- |
Johan den Dunnen |
00466013 |
|
Legend |
How to query |