
 Phenotype ID
|

 Phenotype details
|

 Diagnosis/Initial
|

 Diagnosis/Definite
|

 Inheritance
|

 Age/Examination
|

 Age/Diagnosis
|

 Age/Onset
|

 Phenotype/Onset
|

 Protein
|

 Owner
|

 Individual ID
|
0000026468 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033039 |
0000026472 |
autosomal recessive retinitis pigmentosa (ARRP) |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033043 |
0000026473 |
autosomal recessive retinitis pigmentosa (ARRP) |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033044 |
0000026482 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033053 |
0000026483 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033054 |
0000026485 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033056 |
0000026487 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033058 |
0000026488 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033059 |
0000026489 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033060 |
0000026490 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033061 |
0000026491 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033062 |
0000026493 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033064 |
0000026494 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033065 |
0000026495 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033066 |
0000026497 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033068 |
0000026505 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033076 |
0000026508 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033079 |
0000026509 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033080 |
0000026511 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033082 |
0000026512 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033083 |
0000026513 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033084 |
0000026514 |
- |
- |
- |
Unknown |
- |
- |
- |
- |
- |
Johan den Dunnen |
00033085 |
0000026781 |
- |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Leen Abu Safieh |
00033352 |
0000026785 |
- |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Leen Abu Safieh |
00033356 |
0000026786 |
- |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Leen Abu Safieh |
00033357 |
0000026791 |
gliosis |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Leen Abu Safieh |
00033362 |
0000026792 |
- |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Leen Abu Safieh |
00033363 |
0000026793 |
- |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Leen Abu Safieh |
00033364 |
0000026810 |
Bilateral contaract; keratoconus; Oculodigital Phenomena; Onset Visual loss, Nyctalopia |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033381 |
0000026811 |
Bilateral plasties; Oculodigital Phenomena; Onset Visual loss |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033382 |
0000026812 |
foveal depression; Onset Visual disturbance, nystagmus |
- |
- |
Familial, autosomal recessive |
1y |
- |
- |
- |
- |
Raheel Qamar |
00033383 |
0000026813 |
foveal depression; Onset Visual disturbance, nystagmus |
- |
- |
Familial, autosomal recessive |
5y |
- |
- |
- |
- |
Raheel Qamar |
00033384 |
0000026815 |
Pseudophakic; keratoconus; patches of periphral chorio retinal atrophy; Oculodigital Phenomena; Onset Visual loss, Nyctalopia;Photosensitivity |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033386 |
0000026817 |
Bilateral pigmentary degeneration; significant hyperopia with astigmatism.; Onset Roving nystagmus;sluggish pupils, andphotophobi |
- |
- |
Familial, autosomal recessive |
2y |
- |
- |
- |
- |
Raheel Qamar |
00033388 |
0000026818 |
Bluntedfoveal reflex; minimally attenuatedretinal vessels; andmildpigment dispersion with traces of finemottling; Onset Nystagmus, sluggish pupillary responses andmildhyperopiawith astigmatism |
- |
- |
Familial, autosomal recessive |
8m |
- |
- |
- |
- |
Raheel Qamar |
00033389 |
0000026825 |
Nystagmus; Onset Severe visual loss |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033396 |
0000026826 |
Nystagmus; Onset Severe visual loss |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033397 |
0000026834 |
Nystagmus; mildmottling of maculopathy; high myopia ; Onset Nystagmus |
- |
- |
Familial, autosomal recessive |
2y |
- |
- |
- |
- |
Raheel Qamar |
00033405 |
0000026835 |
- |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033406 |
0000026836 |
foveal depression; Onset Visual disturbance, nystagmus |
- |
- |
Familial, autosomal recessive |
3y |
- |
- |
- |
- |
Raheel Qamar |
00033407 |
0000026837 |
- |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033408 |
0000026838 |
Keratoconus; cataract; foveal depression; Onset Visual disturbance, nystagmus |
- |
- |
Familial, autosomal recessive |
23y |
- |
- |
- |
- |
Raheel Qamar |
00033409 |
0000026839 |
foveal depression; Onset Visual disturbance, nystagmus |
- |
- |
Familial, autosomal recessive |
27y |
- |
- |
- |
- |
Raheel Qamar |
00033410 |
0000026841 |
Retinal drunes like depositions; Oculodigital Phenomena; Onset Visual loss, Nyctalopia |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033412 |
0000026842 |
MildMaculopathy ; Onset Severe pigmentary retinopathy |
- |
- |
Familial, autosomal recessive |
24y |
- |
- |
- |
- |
Raheel Qamar |
00033413 |
0000026843 |
- |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033414 |
0000026844 |
- |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033415 |
0000026845 |
- |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033416 |
0000026846 |
dilatedretinal vessels; mainly venules; primarily localisedin the posterior pole;photoreceptors are absent; retinal gliosis was present; Headache andpain in eyes; Bilateral Nysgtagmus |
- |
- |
Familial, autosomal recessive |
22y |
- |
- |
- |
- |
Raheel Qamar |
00033417 |
0000026847 |
dilatedretinal vessels; mainly venules; primarily localisedin the posterior pole;photoreceptors are absent; retinal gliosis was present; Headache andpain in eyes; Bilateral Nysgtagmus |
- |
- |
Familial, autosomal recessive |
4y |
- |
- |
- |
- |
Raheel Qamar |
00033418 |
0000026848 |
Nystagmus; moderate pigmentry retionopathy;maculopathy atrophy;disc pallor drusen; posterior subcapsular cataract; keratoconus; Onset Poor vision;nystagmus |
- |
- |
Familial, autosomal recessive |
30y |
- |
- |
- |
- |
Raheel Qamar |
00033419 |
0000026849 |
Nystagmus; moderate pigmentry retionopathy;maculopathy atrophy;disc pallor drusen; posterior subcapsular cataract; keratoconus; Onset Poor vision;nystagmus |
- |
- |
Familial, autosomal recessive |
36y |
- |
- |
- |
- |
Raheel Qamar |
00033420 |
0000026850 |
? |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033421 |
0000026857 |
Nystagmus;moderate pigmentry retionpathy;maculopathy atrophy; drusen; presence of white retinal dots; posterior subcapsular cataract; moderate myopia; Onset Poor vision, nystagmus |
- |
- |
Familial, autosomal recessive |
17y |
- |
- |
- |
- |
Raheel Qamar |
00033428 |
0000026858 |
- |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033429 |
0000026859 |
- |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033430 |
0000026862 |
dilatedretinal vessels; mainly venules; primarily localisedin the posterior pole; Headache andpain in eyes; Bilateral Nysgtagmus |
- |
- |
Familial, autosomal recessive |
22y |
- |
- |
- |
- |
Raheel Qamar |
00033433 |
0000026863 |
dilatedretinal vessels; mainly venules; primarily localisedin the posterior pole; Headache andpain in eyes; Bilateral Nysgtagmus |
- |
- |
Familial, autosomal recessive |
4y |
- |
- |
- |
- |
Raheel Qamar |
00033434 |
0000026864 |
Visual fieldchanges; ERG reduction; Onset Nystagmus, |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033435 |
0000026865 |
mild maculopathy; absence of pigmentary retinopathy |
- |
- |
Familial, autosomal recessive |
4m |
- |
- |
- |
- |
Raheel Qamar |
00033436 |
0000026866 |
? |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033437 |
0000026869 |
Pseudophakic; keratoconus; patches of periphral chorio retinal atrophy; Oculodigital Phenomena; Onset Visual loss, Nyctalopia, Photosensitivity, Atrophy of retinal pigment andchoroid, pigmentary clumping |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033440 |
0000026870 |
Keratoconus; Bilateral Contaracts; Oculodigital Phenomena; Onset Visual loss, Nyctalopia;Photosensitivity |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033441 |
0000026875 |
- |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033446 |
0000026876 |
Severe Maculopathy; Moderate pigmentary retinopathy |
- |
- |
Familial, autosomal recessive |
8y |
- |
- |
- |
- |
Raheel Qamar |
00033447 |
0000026877 |
Onset Severe pigmentary Retinopathy |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033448 |
0000026880 |
Onset Severe pigmentary Retinopathy |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033451 |
0000026889 |
Nystagmus; moderate hyperopia; Onset Poor vision;nystagmus |
- |
- |
Familial, autosomal recessive |
2y |
- |
- |
- |
- |
Raheel Qamar |
00033460 |
0000026890 |
MildMaculopathy; Onset Severe pigmentary retinopathy |
- |
- |
Familial, autosomal recessive |
10y |
- |
- |
- |
- |
Raheel Qamar |
00033461 |
0000026891 |
keratoconu; cataracts; pale optic discs;arteriolar attenuation andintraretinal pigment migration; Onset Night blindness |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033462 |
0000026892 |
keratoconu; cataracts; pale optic discs;arteriolar attenuation andintraretinal pigment migration; Onset Night blindness |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033463 |
0000026893 |
? |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033464 |
0000026894 |
? |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033465 |
0000026895 |
? |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033466 |
0000026896 |
? |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033467 |
0000026900 |
Onset Severe pigmentary retinopathy |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033471 |
0000026901 |
- |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033472 |
0000026902 |
- |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033473 |
0000026903 |
? |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033474 |
0000026904 |
? |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033475 |
0000026905 |
? |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033476 |
0000026906 |
? |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033477 |
0000026915 |
MildMaculopathy; Onset Severe pigmentary retinopathy |
- |
- |
Familial, autosomal recessive |
16y |
- |
- |
- |
- |
Raheel Qamar |
00033486 |
0000026921 |
? |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033492 |
0000026922 |
MildMaculopathy; Onset Severe pigmentary retinopathy |
- |
- |
Familial, autosomal recessive |
17y |
- |
- |
- |
- |
Raheel Qamar |
00033493 |
0000026923 |
MildMaculopathy |
- |
- |
Familial, autosomal recessive |
19y |
- |
- |
- |
- |
Raheel Qamar |
00033494 |
0000026924 |
Cataract; foveal depression; Onset Visual disturbance, nystagmus |
- |
- |
Familial, autosomal recessive |
33y |
- |
- |
- |
- |
Raheel Qamar |
00033495 |
0000026925 |
Foveal depression; RPE pigmentation abnormalities; Onset Visual disturbance, nystagmus |
- |
- |
Familial, autosomal recessive |
40y |
- |
- |
- |
- |
Raheel Qamar |
00033496 |
0000026927 |
Bone specule like changes; Bull's eye appearence; Atrophic macular lesions; drusion like deposits; Oculodigital Phenomena; Onset Visual Loss, Severe pigmentary retinopathy, Atrophy of retinal pigment, mottling of hypopigmentation. |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033498 |
0000026928 |
Cataract; Melanin abnormalities; foveal depression; Onset Visual disturbance, nystagmus |
- |
- |
Familial, autosomal recessive |
40y |
- |
- |
- |
- |
Raheel Qamar |
00033499 |
0000026929 |
RPE pigmentation abnormalities; foveal depression; Onset Visual disturbance, nystagmus |
- |
- |
Familial, autosomal recessive |
7y |
- |
- |
- |
- |
Raheel Qamar |
00033500 |
0000026930 |
Melanin abnormalities; foveal depression; Onset Visual disturbance, nystagmus |
- |
- |
Familial, autosomal recessive |
39y |
- |
- |
- |
- |
Raheel Qamar |
00033501 |
0000026931 |
Cataract; retinal degeneration; foveal depression; Onset Visual disturbance, nystagmus, visual acuity, nyctalopia |
- |
- |
Familial, autosomal recessive |
45y |
- |
- |
- |
- |
Raheel Qamar |
00033502 |
0000026946 |
Severe keratoconus; poor acuity; macular atrophy |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033517 |
0000026947 |
Severe keratoconus; poor acuity; macular atrophy |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033518 |
0000026948 |
Severe keratoconus; poor acuity; macular atrophy |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033519 |
0000026949 |
Grossly intact extraocular movement; sluggishpupillary responses; normal intraocular pressure to palpation;andsevere hyperopia with astigmatism.; Onset Nystagmus |
- |
- |
Familial, autosomal recessive |
4m |
- |
- |
- |
- |
Raheel Qamar |
00033520 |
0000026950 |
Nystagmus; Moderate pigmentry retinopathy;bone spicules; mildmolting maculopathy; presence of white retinal dots;myopia; Onset Poor vision, nystagmus |
- |
- |
Familial, autosomal recessive |
19y |
- |
- |
- |
- |
Raheel Qamar |
00033521 |
0000026951 |
Nystagmus; Moderate pigmentry retinopathy;bone spicules; maculopathy atrophy; Onset Poor vision, nystagmus |
- |
- |
Familial, autosomal recessive |
24y |
- |
- |
- |
- |
Raheel Qamar |
00033522 |
0000026952 |
? |
- |
- |
Familial, autosomal recessive |
- |
- |
- |
- |
- |
Raheel Qamar |
00033523 |