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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!="p.0" |
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*|Ter !fs |
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Date |
2020 |
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| |
Date |
2020-03|2020-04 |
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Date |
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< |
Date |
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Date |
<=2020-06 |
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Date |
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>= |
Date |
>=2020-06-15 |
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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 |
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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 |
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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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 Phenotype ID
|

 Phenotype details
|

 Diagnosis/Initial
|

 Diagnosis/Definite
|

 Inheritance
|

 Age/Examination
|

 Age/Diagnosis
|

 Age/Onset
|

 Phenotype/Onset
|

 Protein
|

 Owner
|

 Individual ID
|
0000025153 |
see paper; X-linked infantile cardiomyopathy |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00029119 |
0000025217 |
see paper; X-linked infantile cardiomyopathy |
- |
- |
Familial, X-linked recessive |
- |
- |
- |
- |
- |
Johan den Dunnen |
00029183 |
0000025259 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00029225 |
0000025293 |
- |
- |
- |
Familial |
- |
- |
- |
- |
- |
Johan den Dunnen |
00029259 |
0000039850 |
- |
- |
- |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Andreas Brodehl |
00053148 |
0000044634 |
cardiomyopathy |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00058003 |
0000052676 |
familial neonatal isolated cardiomyopathy; 15 Bedouin patients with familial neonatal isolated cardiomyopathy |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Jean-Pierre Bayley |
00072985 |
0000068416 |
cardiomyopathy, mild |
- |
- |
Familial, X-linked dominant |
- |
- |
- |
- |
- |
Hakan Cetin |
00089012 |
0000079131 |
Cardiomyopathy |
- |
- |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00100912 |
0000079132 |
Cardiomyopathy |
- |
- |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00100913 |
0000079133 |
Cardiomyopathy, late-onset polyneuropathy of lower limbs ? |
- |
- |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Johan den Dunnen |
00100914 |
0000081979 |
severe cardiomyopathy, suspected DMD-carrier, son has DMD (pathogenic variant DMD-gene) |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Andreas Laner |
00035617 |
0000127450 |
- |
cardiomyopathy |
- |
Familial |
- |
- |
- |
- |
- |
Peikuan Cong |
00154714 |
0000127550 |
extensive, diffuse late gadolinium enhancement left ventricle |
cardiomyopathy |
- |
Familial |
- |
- |
- |
- |
- |
Peikuan Cong |
00154814 |
0000128983 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Judith Verhagen |
00163871 |
0000128985 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Judith Verhagen |
00163873 |
0000129009 |
- |
- |
- |
Isolated (sporadic) |
- |
82y |
- |
- |
- |
Judith Verhagen |
00163897 |
0000129011 |
atrial fibrillation (HP:0005110), paroxysmal ventricular tachycardia (HP:0004751), first degree atrioventricular block (HP:0011705) |
- |
- |
Isolated (sporadic) |
- |
53y |
- |
- |
- |
Judith Verhagen |
00163899 |
0000157806 |
left-dominant arrhythmogenic cardiomyopathy |
left-dominant arrhythmogenic cardiomyopathy |
CMD-1BB |
Unknown |
- |
- |
- |
- |
- |
Paul van der Zwaag |
00209200 |
0000157938 |
left-dominant arrhythmogenic cardiomyopathy |
left-dominant arrhythmogenic cardiomyopathy |
- |
Unknown |
- |
- |
- |
- |
- |
Paul van der Zwaag |
00209339 |
0000157940 |
left-dominant arrhythmogenic cardiomyopathy |
left-dominant arrhythmogenic cardiomyopathy |
- |
Unknown |
- |
- |
- |
- |
- |
Paul van der Zwaag |
00209341 |
0000157942 |
left-dominant arrhythmogenic cardiomyopathy |
left-dominant arrhythmogenic cardiomyopathy |
- |
Unknown |
- |
- |
- |
- |
- |
Paul van der Zwaag |
00209343 |
0000157944 |
left-dominant arrhythmogenic cardiomyopathy |
left-dominant arrhythmogenic cardiomyopathy |
- |
Unknown |
- |
- |
- |
- |
- |
Paul van der Zwaag |
00209345 |
0000157948 |
left-dominant arrhythmogenic cardiomyopathy |
left-dominant arrhythmogenic cardiomyopathy |
- |
Unknown |
- |
- |
- |
- |
- |
Paul van der Zwaag |
00209349 |
0000157949 |
left-dominant arrhythmogenic cardiomyopathy |
left-dominant arrhythmogenic cardiomyopathy |
- |
Unknown |
- |
- |
- |
- |
- |
Paul van der Zwaag |
00209350 |
0000158012 |
cardiomyopathy |
cardiomyopathy |
- |
Unknown |
- |
- |
- |
- |
- |
Paul van der Zwaag |
00209413 |
0000158246 |
left-dominant arrhythmogenic cardiomyopathy |
left-dominant arrhythmogenic cardiomyopathy |
ARVD-9 |
Unknown |
- |
- |
- |
- |
- |
Paul van der Zwaag |
00209647 |
0000160513 |
Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. |
cardiomyopathy, dilated/hypertrophic |
- |
Unknown |
- |
- |
- |
- |
- |
Peikuan Cong |
00212031 |
0000160521 |
dilated/hypertrophic |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Peikuan Cong |
00212039 |
0000160536 |
- |
cardiomyopathy, hpertrophic, left ventricular |
- |
Unknown |
- |
- |
- |
- |
- |
Peikuan Cong |
00212054 |
0000160598 |
Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. |
cardiomyopathy, dilated/hypertrophic |
- |
Unknown |
- |
- |
- |
- |
- |
Peikuan Cong |
00212116 |
0000160722 |
Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. |
cardiomyopathy, dilated/hypertrophic |
- |
Unknown |
- |
- |
- |
- |
- |
Peikuan Cong |
00212240 |
0000160774 |
2/3 died as child <3y from cardiomyopathy |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212292 |
0000160775 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212293 |
0000160776 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212294 |
0000160795 |
Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. |
cardiomyopathy, dilated/hypertrophic |
- |
Unknown |
- |
- |
- |
- |
- |
Peikuan Cong |
00212313 |
0000160810 |
Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. |
cardiomyopathy, dilated/hypertrophic |
- |
Unknown |
- |
- |
- |
- |
- |
Peikuan Cong |
00212328 |
0000160811 |
Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. |
cardiomyopathy, dilated/hypertrophic |
- |
Unknown |
- |
- |
- |
- |
- |
Peikuan Cong |
00212329 |
0000160854 |
Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. |
cardiomyopathy, dilated/hypertrophic |
- |
Unknown |
- |
- |
- |
- |
- |
Peikuan Cong |
00212372 |
0000160867 |
Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. |
cardiomyopathy, dilated/hypertrophic |
- |
Unknown |
- |
- |
- |
- |
- |
Peikuan Cong |
00212385 |
0000160878 |
Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. |
cardiomyopathy, dilated/hypertrophic |
- |
Unknown |
- |
- |
- |
- |
- |
Peikuan Cong |
00212396 |
0000160881 |
- |
cardiomyopathy |
CMH-4 |
Familial |
- |
- |
- |
- |
- |
Peikuan Cong |
00212399 |
0000160904 |
Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. |
cardiomyopathy, dilated/hypertrophic |
- |
Unknown |
- |
- |
- |
- |
- |
Peikuan Cong |
00212422 |
0000160905 |
dilated/hypertrophic |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Peikuan Cong |
00212423 |
0000160927 |
Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. |
cardiomyopathy, dilated/hypertrophic |
- |
Unknown |
- |
- |
- |
- |
- |
Peikuan Cong |
00212445 |
0000160938 |
Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. |
cardiomyopathy, dilated/hypertrophic |
- |
Unknown |
- |
- |
- |
- |
- |
Peikuan Cong |
00212456 |
0000160957 |
Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. |
cardiomyopathy, dilated/hypertrophic |
- |
Unknown |
- |
- |
- |
- |
- |
Peikuan Cong |
00212475 |
0000160966 |
Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. |
cardiomyopathy, dilated/hypertrophic |
- |
Unknown |
- |
- |
- |
- |
- |
Peikuan Cong |
00212484 |
0000160972 |
Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. |
cardiomyopathy, dilated/hypertrophic |
- |
Unknown |
- |
- |
- |
- |
- |
Peikuan Cong |
00212490 |
0000160984 |
Mutations in MYBPC3 encoding myosin binding protein C belong to the most frequent causes of hypertrophic cardiomyopathy (HCM) and may also lead to dilated cardiomyopathy (DCM). MYBPC3 mutations initially were considered to cause a benign form of HCM. The aim of this study was to examine the clinical outcome of patients and their relatives with 18 different MYBPC3 mutations. |
cardiomyopathy, dilated/hypertrophic |
- |
Unknown |
- |
- |
- |
- |
- |
Peikuan Cong |
00212502 |
0000160986 |
dilated/hypertrophic |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Peikuan Cong |
00212504 |
0000161003 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212521 |
0000161004 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212522 |
0000161005 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212523 |
0000161006 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212524 |
0000161007 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212525 |
0000161008 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212526 |
0000161009 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212527 |
0000161010 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212528 |
0000161011 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212529 |
0000161012 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212530 |
0000161013 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212531 |
0000161014 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212532 |
0000161015 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212533 |
0000161016 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212534 |
0000161017 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212535 |
0000161018 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212536 |
0000161019 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212537 |
0000161020 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212538 |
0000161021 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212539 |
0000161022 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212540 |
0000161023 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212541 |
0000161024 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212542 |
0000161025 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212543 |
0000161026 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212544 |
0000161027 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212545 |
0000161028 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212546 |
0000161029 |
- |
cardiomyopathy |
CMH-4 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212547 |
0000161175 |
- |
cardiomyopathy; myopathy, distal |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212693 |
0000161203 |
- |
cardiomyopathy |
CMH-1 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212721 |
0000161277 |
- |
cardiomyopathy; myopathy, distal |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212795 |
0000161291 |
- |
cardiomyopathy |
CMH-1 |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00212809 |
0000165373 |
- |
cardiomyopathy |
- |
- |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216922 |
0000165374 |
- |
cardiomyopathy |
- |
- |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216923 |
0000165375 |
- |
cardiomyopathy |
- |
- |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216924 |
0000165376 |
- |
cardiomyopathy |
- |
- |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216925 |
0000165377 |
- |
cardiomyopathy |
- |
- |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216926 |
0000165378 |
- |
cardiomyopathy |
- |
- |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216927 |
0000165379 |
- |
cardiomyopathy |
- |
- |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216928 |
0000165380 |
- |
cardiomyopathy |
- |
- |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216929 |
0000165381 |
- |
cardiomyopathy |
- |
- |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216930 |
0000165382 |
- |
cardiomyopathy |
- |
- |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216931 |
0000165383 |
- |
cardiomyopathy |
- |
- |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216932 |
0000165384 |
- |
cardiomyopathy |
- |
- |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216933 |
0000165385 |
- |
cardiomyopathy |
- |
- |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216934 |
0000165386 |
- |
cardiomyopathy |
- |
- |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216935 |
0000165387 |
- |
cardiomyopathy |
- |
- |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216936 |
0000165388 |
- |
cardiomyopathy |
- |
- |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216937 |
0000165389 |
- |
cardiomyopathy |
- |
- |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216938 |
0000165390 |
- |
cardiomyopathy |
- |
- |
- |
- |
- |
- |
- |
Johan den Dunnen |
00216939 |
|
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