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Phenotypes for disease #05098 (RCM (cardiomyopathy, restrictive (RCM)))
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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30 entries on 1 page. Showing entries 1 - 30.
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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
0000039844
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Andreas Brodehl
00053142
0000039845
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Andreas Brodehl
00053143
0000045047
-
-
-
Familial, autosomal dominant
-
-
-
-
-
Claire Chauveau
00058416
0000081308
-
-
-
Unknown
-
-
-
-
-
Andreas Brodehl
00103211
0000127278
-
cardiomyopathy, restrictive
-
Familial, autosomal dominant
-
-
-
-
-
Peikuan Cong
00154542
0000127279
died of heart failure; marked bi-atrial dilatation, dilatation of pulmonary veins, normal-sized ventricles, normal wall thickness; ECG sinus rhythm with prominent P-waves, T-wave inversions, incomplete right bundle branch block; heart myocyte hypertrophy, abundant interstitial fibrosis, myofibril disarray
cardiomyopathy, restrictive
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00154543
0000127280
-
cardiomyopathy, restrictive
-
Isolated (sporadic)
-
-
-
-
-
Peikuan Cong
00154544
0000127281
-
cardiomyopathy, restrictive
-
Isolated (sporadic)
-
-
-
-
-
Peikuan Cong
00154545
0000127282
-
cardiomyopathy, restrictive
-
Isolated (sporadic)
-
-
-
-
-
Peikuan Cong
00154546
0000127283
-
cardiomyopathy, restrictive
-
Isolated (sporadic)
-
-
-
-
-
Peikuan Cong
00154547
0000127284
sudden death father
cardiomyopathy, restrictive
-
Isolated (sporadic)
-
-
-
-
-
Peikuan Cong
00154548
0000127341
-
cardiomyopathy, restrictive
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00154605
0000127344
-
cardiomyopathy, restrictive
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00154608
0000127345
-
cardiomyopathy, restrictive
-
Isolated (sporadic)
-
-
-
-
-
Johan den Dunnen
00154609
0000127361
ventricular septal defect
cardiomyopathy, restrictive
-
Isolated (sporadic)
-
-
4y
-
-
Peikuan Cong
00154625
0000127376
-
cardiomyopathy, restrictive
-
Familial
-
-
-
-
-
Johan den Dunnen
00154640
0000127377
severe
cardiomyopathy, restrictive
-
Isolated (sporadic)
-
-
6m
-
-
Johan den Dunnen
00154641
0000127387
-
cardiomyopathy, restrictive
-
Unknown
-
-
-
-
-
Johan den Dunnen
00154651
0000127397
-
cardiomyopathy, restrictive
-
Familial
-
-
-
-
-
Johan den Dunnen
00154661
0000127410
sudden caridac death
cardiomyopathy, restrictive
-
Unknown
-
-
-
-
-
Johan den Dunnen
00154674
0000127548
-
cardiomyopathy, restrictive
-
Unknown
-
-
-
-
-
Peikuan Cong
00154812
0000152791
Paroxysmal atrial fibrillation (HP:0004757), Mitral regurgitation (HP:0001653), Ischemic stroke (HP:0002140)
-
-
Familial, autosomal recessive
41y
41y
-
Exertional dyspnea (HP:0002875)
-
Malena Pantou
00204288
0000155798
-
resctrictive cardiomyopathy
-
Unknown
-
-
-
-
-
Johan den Dunnen
00208029
0000158783
carrier mother MYL2:G57E and MYL3:E143K
restrictive cardiomyopathy
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00210217
0000158835
carrier mother MYL2:G57E and MYL3:E143K
restrictive cardiomyopathy
-
Familial, autosomal recessive
-
-
-
-
-
Johan den Dunnen
00210269
0000161247
-
restrictive cardiomyopathy
-
Unknown
-
-
-
-
-
Johan den Dunnen
00212765
0000165347
mitral regurgitation (MR), tricuspid regurgitation (TR), atrial fibrillation (AF), 11 years, heart transplant
restrictive cardiomyopathy
CMD-1KK
Familial
-
-
7y
-
-
Julia Lopez
00216896
0000165348
mitral regurgitation (MR), 9 years, heart transplant
restrictive cardiomyopathy
CMD-1KK
Familial
-
-
8y
-
-
Julia Lopez
00216897
0000170740
right sided-dominant heart failure; right ventricular dilatation, mild (HP:0005133); increased adipose tissue (HP:0009126); cardiomyocyte hypertrophy, mild (HP:0031319); myocardial fibrosis, mild (HP:0001685); restrictive cardiomyopathy (HP:0001723); pulmonary arterial hypertension (HP:0002092); tricuspid regurgitation, moderate (HP:0005180); left atrial enlargement (HP:0031295); right atrial enlargement (HP:0030718); right bundle branch block, incomplete (HP:0011712); paroxysmal atrial fibrillation (HP:0004757); peripheral edema (HP:0012398); elevated jugular venous pressure (HP:0030848); hepatojugular reflux (HP:0030849)
-
-
Familial, autosomal dominant
30y
24y
-
-
-
Jilani Jawaid
00225627
0000170743
atrial fibrillation (HP:0005110); atrioventricular block (HP:0001678); exertional dyspnea (HP:0002875); left atrial enlargement (HP:0031295); right atrial enlargement (HP:0030718); increased NT-proBNP level (HP:0031185); Cardiomyocyte hypertrophy (HP:0031319); interstitial cardiac fibrosis (HP:0031329); muscle weakness (HP:0001324); exercise-induced muscle fatigue (HP:0009020); myalgia (HP:0003326); areflexia (HP:0001284); nonocclusive coronary artery atherosclerosis (HP:0012436); increased endomysial connective tissue, esp. biceps brachii (HP:0100297); abnormality of skeletal muscle fiber size, esp. biceps brachii (HP:0012084); muscle fiber necrosis, esp. biceps brachii (HP:0003713); regenerating fibres, esp. biceps brachii
-
-
Unknown
63y
53y
45y
-
-
Jilani Jawaid
00225633
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