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
|
0000116533 |
- |
- |
- |
Familial, autosomal recessive |
01y |
- |
- |
- |
- |
Dr. Alexandra Wey-Fabrizius |
00143763 |
0000209190 |
bilateral retinal detachment (HP:0000541), severe osteopenia (HP:0000938) |
- |
osteoporosis-pseudoglioma syndrome |
Familial, autosomal dominant |
08y |
- |
01y |
retinal detachment (HP:0000541) |
- |
Jasmine Chen |
00274228 |
0000209231 |
microphthalmia (HP:0000568), fractures (HP:0002757) |
- |
osteoporosis-pseudoglioma syndrome |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Jasmine Chen |
00274289 |
0000254185 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Johan den Dunnen |
00107585 |
0000254186 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Johan den Dunnen |
00107594 |
0000254187 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Johan den Dunnen |
00107600 |
0000254188 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Johan den Dunnen |
00107606 |
0000254189 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Johan den Dunnen |
00107607 |
0000254190 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Johan den Dunnen |
00107608 |
0000254191 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Johan den Dunnen |
00107609 |
0000254192 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Johan den Dunnen |
00107610 |
0000254193 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Johan den Dunnen |
00107611 |
0000254194 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Johan den Dunnen |
00107612 |
0000254195 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00107614 |
0000254196 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Familial |
- |
- |
- |
- |
- |
Frans Cremers |
00107666 |
0000254197 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Familial |
- |
- |
- |
- |
- |
Frans Cremers |
00107667 |
0000254198 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Familial |
- |
- |
- |
- |
- |
Frans Cremers |
00107668 |
0000254199 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Familial |
- |
- |
- |
- |
- |
Frans Cremers |
00107669 |
0000254200 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Familial |
- |
- |
- |
- |
- |
Frans Cremers |
00107670 |
0000254201 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Familial |
- |
- |
- |
- |
- |
Frans Cremers |
00107671 |
0000254202 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Familial |
- |
- |
- |
- |
- |
Frans Cremers |
00107672 |
0000254203 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Familial |
- |
- |
- |
- |
- |
Frans Cremers |
00107673 |
0000254204 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Familial |
- |
- |
- |
- |
- |
Frans Cremers |
00107674 |
0000254205 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Familial |
- |
- |
- |
- |
- |
Frans Cremers |
00107675 |
0000254206 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Familial |
- |
- |
- |
- |
- |
Frans Cremers |
00107676 |
0000254207 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Familial |
- |
- |
- |
- |
- |
Frans Cremers |
00107677 |
0000254208 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Familial |
- |
- |
- |
- |
- |
Frans Cremers |
00107678 |
0000254209 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Familial |
- |
- |
- |
- |
- |
Frans Cremers |
00107679 |
0000254210 |
osteoporosis-pseudoglioma syndrome, congenital pseudoglioma, fractures (6y), no mental retardation |
- |
osteoporosis-pseudoglioma syndrome |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Frans Cremers |
00107680 |
0000254211 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Familial |
- |
- |
- |
- |
- |
Frans Cremers |
00107682 |
0000254212 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Familial |
- |
- |
- |
- |
- |
Frans Cremers |
00107683 |
0000254213 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Familial |
- |
- |
- |
- |
- |
Frans Cremers |
00107684 |
0000254214 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Isolated (sporadic) |
- |
- |
- |
- |
- |
Frans Cremers |
00107686 |
0000254215 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Familial |
- |
- |
- |
- |
- |
Frans Cremers |
00107687 |
0000254216 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Familial |
- |
- |
- |
- |
- |
Frans Cremers |
00107688 |
0000254217 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Unknown |
- |
- |
- |
- |
- |
Frans Cremers |
00107689 |
0000254218 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Familial |
- |
- |
- |
- |
- |
Frans Cremers |
00107690 |
0000254219 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Familial |
- |
- |
- |
- |
- |
Frans Cremers |
00107691 |
0000254220 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Familial |
- |
- |
- |
- |
- |
Frans Cremers |
00107692 |
0000254221 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Unknown |
- |
- |
- |
- |
- |
Frans Cremers |
00107693 |
0000254222 |
primary osteoporosis;osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Familial |
- |
- |
- |
- |
- |
Frans Cremers |
00107703 |
0000254223 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Familial |
- |
- |
- |
- |
- |
Frans Cremers |
00107708 |
0000254224 |
osteoporosis-pseudoglioma syndrome |
- |
osteoporosis-pseudoglioma syndrome |
Familial |
- |
- |
- |
- |
- |
Frans Cremers |
00107709 |
0000308379 |
familial exudative vitreoretinopathy stage 5 right eye 4B left eye (HP:0030490), osteopenia (HP:0000938); early onset nystagmus with severe retinopathy and rapid development of retinal detachment in the left eye; 1y: pars plana vitrectomy and Argon laser photocoagulation in the right eye for stage 4B familial exudative vitreoretinopathy (retinal detachment involving the macula with falciform fold anchored in the temporal retinal sector and abnormal peripheral exudation); left eye was too advanced due to stage 5 familial exudative vitreoretinopathy (closed funnel retinal detachment); 3y: cataract surgery with intraocular lens implant resulting in stable visual acuity of 0.6 LogMAR in the right eye for the next 3 years; 7y: sudden visual loss (1.0 LogMAR) fluorangiography: retinal exudation next to the falciform fold in the macular area, underwent retinal cryotreatment; subsequent examination showed reabsorption of the exudates and no signs of angiographic leakage; visual acuity restored to 0.6 LogMAR; total X-ray examination of the proband showed thin, elongated diaphyses of the long bones with relatively wider metaphyses, valgus deviation of the femoral neck- diaphysis axis, evident reduction in calcium tone and no other skeletal alterations; dual energy X-ray absorptiometry (DXA): L1 to L4 bone mineral density as 0.4 g/cm2 (Z-score: -1.8); familial exudative vitreoretinopathy stage right/left eye: 4B/5; bone mineral density: osteopenia |
- |
osteoporosis-pseudoglioma syndrome (OPPG) |
Familial |
07y |
01y |
- |
- |
- |
LOVD |
00416869 |
0000308380 |
stage 2 FEVR (HP:0030490), osteopenia (HP:0000938); fundus: very small hard peripheral exudates; fluorescein angiography: evidence of stage 2A familial exudative vitreoretinopathy; dual energy X-ray absorptiometry: L1 to L4 bone mineral density: 1.033 g/ cm2 (Z-score: -1.5 SD) and left total femur and neck bone mineral density were 0.905 g/cm2 (Z-score: -1.3 SD) and 0.822 g/cm2 (Z score: -1.7 SD), respectively; familial exudative vitreoretinopathy stage right/left eye: 2A/2A; bone mineral density: osteopenia |
- |
osteoporosis-pseudoglioma syndrome (OPPG) |
Familial |
46y |
- |
- |
- |
- |
LOVD |
00416870 |
0000308381 |
FEVR (HP:0030490), severe osteoporosis (HP:0000939); familial exudative vitreoretinopathy stage right/left eye: 5A/3B; bone mineral density: osteoporosis; 1m: retinopathy from the first month of life with complete retinal detachment in the right eye; 10m: fundus examination conducted under general anesthesia: familial exudative vitreoretinopathy diagnosis, stage right/left eye: 5A/3B; total retinal detachment right eye with disorganised proliferative tissue; vitreoretinal surgery with lensectomy, vitrectomy and membrane peeling; radial retinal fold associated with a small area of persistent vascularization extending into the vitreal cavity in the left eye; lest eye fluorescein angiography: wide area of the peripheral retina devoid of vascularization and with vascular leakage treated by Argon laser ablation; bone mineral density: severe osteoporosis; current whole body bone mineral density: 0.5 g/cm2 (Z-score: -2.5 SD) |
- |
osteoporosis-pseudoglioma syndrome (OPPG) |
Familial |
04y |
00y10m |
00y01m |
- |
- |
LOVD |
00416871 |
0000308382 |
no familial exudative vitreoretinopathy; bone mineral density: osteopenia - lumbar bone mineral density of 0.966 g/cm2 (Z-score: -1.1 SD) |
- |
osteoporosis-pseudoglioma syndrome (OPPG) |
Familial, autosomal dominant |
31y |
- |
- |
- |
- |
LOVD |
00416872 |
0000308383 |
no familial exudative vitreoretinopathy, no osteopenia; lumbar bone mineral density of 1.199 g/cm2 (Z-score: 1.4 SD) |
- |
osteoporosis-pseudoglioma syndrome (OPPG) |
Familial, autosomal dominant |
31y |
- |
- |
- |
- |
LOVD |
00416873 |
|
Legend |
How to query |