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
|
0000046591 |
age presentation late 50s ; fundus myopic degeneration, peripapillary atrophy ; fundus autofluorescence imaging normal foveal; foveal appearance on spectral‐domain optical coherence tomography myopic changes ; full‐field electroretinograms normal; pattern electroretinogram P50 components severely subnormal |
- |
- |
Unknown |
78y |
- |
- |
- |
- |
Alice Davidson |
00060101 |
0000046592 |
age presentation 20s ; fundus normal ; fundus autofluorescence imaging normal; foveal appearance on spectral‐domain optical coherence tomography irregular ISe line ; full‐field electroretinograms normal; pattern electroretinogram P50 components severely subnormal |
- |
- |
Unknown |
47y |
- |
- |
- |
- |
Alice Davidson |
00060102 |
0000046593 |
age presentation 40s ; fundus normal ; fundus autofluorescence imaging irregular foveal; foveal appearance on spectral‐domain optical coherence tomography focal disruption of the ISe line in the foveola; irregular ISe line ; Scotopic full‐field electroretinograms normal; photopic 30 Hz ERG mildly delayed. pattern electroretinogram P50 components subnormal |
- |
- |
Unknown |
52y |
- |
- |
- |
- |
Alice Davidson |
00060103 |
0000046594 |
age presentation early 50s ; fundus normal ; fundus autofluorescence imaging normal; foveal appearance on spectral‐domain optical coherence tomography not available ; Scotopic full‐field electroretinograms normal; photopic 30 Hz ERG mildly delayed; pattern electroretinogram P50 components severely subnormal; central multifocal electroretinograms subnormal |
- |
- |
Unknown |
67y |
- |
- |
- |
- |
Alice Davidson |
00060104 |
0000046595 |
age presentation late 20s ; fundus normal ; fundus autofluorescence imaging irregular foveal; foveal appearance on spectral‐domain optical coherence tomography focal disruption of the ISe line in the foveola; irregular ISe line; significant thinning ; full‐field electroretinograms normal; pattern electroretinogram P50 components severely subnormal; widespread multifocal electroretinograms reduction |
- |
- |
Unknown |
31y |
- |
- |
- |
- |
Alice Davidson |
00060105 |
0000046596 |
age presentation first decade of life ; fundus normal right eye, small area of atrophy left eye (coloboma) ; fundus autofluorescence imaging irregular foveal, consistent with coloboma left eye; foveal appearance on spectral‐domain optical coherence tomography focal disruption of the ISe line in the foveola of re; consistent with coloboma in the le ; full‐field electroretinograms normal; pattern electroretinogram P50 components subnormal; central multifocal electroretinograms subnormal. |
- |
- |
Unknown |
31y |
- |
- |
- |
- |
Alice Davidson |
00060106 |
0000046597 |
age presentation 15y; fundus normal ; fundus autofluorescence imaging irregular foveal; foveal appearance on spectral‐domain optical coherence tomography disruption of the ISe line ; full‐field electroretinograms normal; pattern electroretinogram P50 components normal; central multifocal electroretinograms markedly subnormal |
- |
- |
Unknown |
31y |
- |
- |
- |
- |
Alice Davidson |
00060107 |
0000046598 |
age presentation late 30s ; fundus normal ; fundus autofluorescence imaging normal; foveal appearance on spectral‐domain optical coherence tomography focal disruption of the ISe line in the foveola; irregular ISe line ; full‐field electroretinograms normal; pattern electroretinogram P50 components subnormal; central multifocal electroretinograms abnormal |
- |
- |
Unknown |
42y |
- |
- |
- |
- |
Alice Davidson |
00060108 |
0000046599 |
age presentation late 60s ; fundus normal ; fundus autofluorescence imaging irregular foveal; foveal appearance on spectral‐domain optical coherence tomography focal disruption of the ISe line in the foveola; irregular ISe line ; full‐field electroretinograms normal; pattern electroretinogram P50 components subnormal |
- |
- |
Unknown |
74y |
- |
- |
- |
- |
Alice Davidson |
00060109 |
0000046600 |
age presentation mid 20s ; fundus normal ; fundus autofluorescence imaging irregular foveal; foveal appearance on spectral‐domain optical coherence tomography focal disruption of the ISe line in the foveola; irregular ISe line ; Normal full‐field electroretinogramss; pattern electroretinogram P50 components severely subnormal |
- |
- |
Unknown |
35y |
- |
- |
- |
- |
Alice Davidson |
00060110 |
0000253967 |
asymptomatic; fundus normal ; fundus autofluorescence imaging normal; foveal appearance on spectral‐domain optical coherence tomography normal ; full‐field electroretinograms normal; pattern electroretinogram P50 components normal; multifocal electroretinograms normal |
occult macular dystrophy |
- |
Unknown |
57y |
- |
- |
- |
- |
LOVD |
00358752 |
0000253968 |
age presentation asymptomatic; fundus normal ; fundus autofluorescence imaging normal; foveal appearance on spectral‐domain optical coherence tomography normal ; Not availabl |
occult macular dystrophy |
- |
Unknown |
29y |
- |
- |
- |
- |
LOVD |
00358753 |
0000253969 |
asymptomatic; fundus normal right eye macular drusen, left eye epiretinal membrane ; fundus autofluorescence imaging normal; foveal appearance on spectral‐domain optical coherence tomography consistent with re macular drusen and le epiretinal membrane ; full‐field electroretinograms normal; pattern electroretinogram P50 components normal on left and mildly subnormal on right normal central multifocal electroretinogramss but mildly subnormal paracentral multifocal electroretinograms right eye |
occult macular dystrophy |
- |
Unknown |
73y |
- |
- |
- |
- |
LOVD |
00358754 |
0000253970 |
asymptomatic; fundus normal ; fundus autofluorescence imaging normal; foveal appearance on spectral‐domain optical coherence tomography normal ; full‐field electroretinograms normal; pattern electroretinogram P50 components normal central; multifocal electroretinograms normal |
occult macular dystrophy |
- |
Unknown |
67y |
- |
- |
- |
- |
LOVD |
00358755 |
0000253971 |
ERG-full field normal, central dysfunction; funduscopy normal; spectral‐domain optical coherence tomography blurring ellipsoid zone, absence interdigitation zone |
occult macular dystrophy |
- |
Familial, autosomal dominant |
14y |
- |
7y |
- |
- |
LOVD |
00358756 |
0000253972 |
ERG-full field normal, central dysfunction; funduscopy normal; spectral‐domain optical coherence tomography blurring ellipsoid zone, absence interdigitation zone |
occult macular dystrophy |
- |
Familial, autosomal dominant |
45y |
- |
40y |
- |
- |
LOVD |
00358757 |
0000253973 |
ERG-full field normal, central dysfunction; funduscopy normal; spectral‐domain optical coherence tomography blurring ellipsoid zone, absence interdigitation zone |
occult macular dystrophy |
- |
Isolated (sporadic) |
31y |
- |
25y |
- |
- |
LOVD |
00358758 |
0000253974 |
ERG-full field normal, central dysfunction; funduscopy normal; spectral‐domain optical coherence tomography blurring ellipsoid zone, absence interdigitation zone |
occult macular dystrophy |
- |
Isolated (sporadic) |
36y |
- |
20y |
- |
- |
LOVD |
00358759 |
0000253975 |
ERG-full field normal, central dysfunction; funduscopy pale disc; spectral‐domain optical coherence tomography blurring ellipsoid zone, absence interdigitation zone |
occult macular dystrophy |
- |
Familial, autosomal dominant |
46y |
- |
33y |
- |
- |
LOVD |
00358760 |
0000253976 |
ERG-full field normal, central dysfunction; funduscopy normal; spectral‐domain optical coherence tomography blurring ellipsoid zone, absence interdigitation zone |
occult macular dystrophy |
- |
Isolated (sporadic) |
42y |
- |
34y |
- |
- |
LOVD |
00358761 |
0000253977 |
ERG-full field normal, central dysfunction; funduscopy normal; spectral‐domain optical coherence tomography blurring ellipsoid zone, absence interdigitation zone |
occult macular dystrophy |
- |
Isolated (sporadic) |
42y |
- |
38y |
- |
- |
LOVD |
00358762 |
0000253978 |
ERG-full field normal, central dysfunction; funduscopy pale disc; spectral‐domain optical coherence tomography blurring ellipsoid zone, absence interdigitation zone |
occult macular dystrophy |
- |
Familial, autosomal dominant |
49y |
- |
48y |
- |
- |
LOVD |
00358763 |
0000253979 |
ERG-full field normal, central dysfunction; funduscopy pale disc; spectral‐domain optical coherence tomography blurring ellipsoid zone, absence interdigitation zone |
occult macular dystrophy |
- |
Familial, autosomal dominant |
79y |
- |
79y |
- |
- |
LOVD |
00358764 |
0000253980 |
ERG-full field normal, central dysfunction; funduscopy normal; spectral‐domain optical coherence tomography no blurring ellipsoid zone, absence interdigitation zone |
occult macular dystrophy |
- |
Familial, autosomal dominant |
48y |
- |
30y |
- |
- |
LOVD |
00358765 |
0000253981 |
ERG-full field normal, central dysfunction; funduscopy normal; spectral‐domain optical coherence tomography blurring ellipsoid zone, absence interdigitation zone |
occult macular dystrophy |
- |
Familial, autosomal dominant |
51y |
- |
25y |
- |
- |
LOVD |
00358766 |
0000253982 |
ERG-full field normal, central dysfunction; funduscopy normal; spectral‐domain optical coherence tomography blurring ellipsoid zone, absence interdigitation zone |
occult macular dystrophy |
- |
Isolated (sporadic) |
52y |
- |
48y |
- |
- |
LOVD |
00358767 |
0000253983 |
ERG-full field normal, central dysfunction; funduscopy normal; spectral‐domain optical coherence tomography blurring ellipsoid zone, absence interdigitation zone |
occult macular dystrophy |
- |
Isolated (sporadic) |
52y |
- |
45y |
- |
- |
LOVD |
00358768 |
0000253984 |
ERG-full field normal, central dysfunction; funduscopy normal; spectral‐domain optical coherence tomography no blurring ellipsoid zone, no absence interdigitation zone |
occult macular dystrophy |
- |
Isolated (sporadic) |
52y |
- |
44y |
- |
- |
LOVD |
00358769 |
0000253985 |
ERG-full field normal, central dysfunction; funduscopy normal; spectral‐domain optical coherence tomography no blurring ellipsoid zone, no absence interdigitation zone |
occult macular dystrophy |
- |
Isolated (sporadic) |
58y |
- |
53y |
- |
- |
LOVD |
00358770 |
0000253986 |
ERG-full field normal, central dysfunction; funduscopy normal; spectral‐domain optical coherence tomography blurring ellipsoid zone, absence interdigitation zone |
occult macular dystrophy |
- |
Familial, autosomal dominant |
54y |
- |
40y |
- |
- |
LOVD |
00358771 |
0000253987 |
ERG-full field normal, central dysfunction; funduscopy normal; spectral‐domain optical coherence tomography no blurring ellipsoid zone, absence interdigitation zone |
occult macular dystrophy |
- |
Isolated (sporadic) |
64y |
- |
62y |
- |
- |
LOVD |
00358772 |
0000253988 |
ERG-full field normal, central dysfunction; funduscopy normal; spectral‐domain optical coherence tomography no blurring ellipsoid zone, no absence interdigitation zone |
occult macular dystrophy |
- |
Isolated (sporadic) |
57y |
- |
47y |
- |
- |
LOVD |
00358773 |
0000253989 |
ERG-full field normal, central dysfunction; funduscopy normal; spectral‐domain optical coherence tomography no blurring ellipsoid zone, no absence interdigitation zone |
occult macular dystrophy |
- |
Familial, autosomal dominant |
58y |
- |
48y |
- |
- |
LOVD |
00358774 |
0000253990 |
ERG-full field normal, central dysfunction; funduscopy normal; spectral‐domain optical coherence tomography blurring ellipsoid zone, absence interdigitation zone |
occult macular dystrophy |
- |
Familial, autosomal dominant |
65y |
- |
61y |
- |
- |
LOVD |
00358775 |
0000253991 |
ERG-full field normal, central dysfunction; funduscopy hard drusen; spectral‐domain optical coherence tomography no blurring ellipsoid zone, no absence interdigitation zone |
occult macular dystrophy |
- |
Isolated (sporadic) |
69y |
- |
64y |
- |
- |
LOVD |
00358776 |
0000253992 |
ERG-full field normal, central dysfunction; funduscopy normal; spectral‐domain optical coherence tomography no blurring ellipsoid zone, absence interdigitation zone |
occult macular dystrophy |
- |
Isolated (sporadic) |
72y |
- |
40y |
- |
- |
LOVD |
00358777 |
0000253993 |
ERG-full field normal, central dysfunction; funduscopy normal; spectral‐domain optical coherence tomography no blurring ellipsoid zone, absence interdigitation zone |
occult macular dystrophy |
- |
Isolated (sporadic) |
66y |
- |
60y |
- |
- |
LOVD |
00358778 |
0000273649 |
HP:0030515, HP:0001123, HP:0030636, HP:0011003 |
dystrophy, macular, occult (OCMD) |
- |
Familial, autosomal dominant |
- |
- |
- |
- |
- |
Jinu Han |
00379794 |
0000296585 |
Retinal dystrophy, Abnormality of metabolism/homeostasis, Somatic sensory dysfunction, Deep white matter hypodensities, Periventricular white matter hyperintensities, Optic neuritis |
- |
- |
Unknown |
09y |
- |
- |
- |
- |
Andreas Laner |
00403992 |
|
Legend |
How to query |