Search results for prph2

134 hits were found for prph2

# Family MCID Name MIFTS Score
1
c STR084 Stargardt Disease 1 54 64.953
2
P RTN008 Retinitis Pigmentosa 79 48.468
3
P CNR004 Cone-Rod Dystrophy 2 74 46.343
4
c MCL060 Macular Dystrophy, Vitelliform, 3 41 44.315
5
c MCL059 Macular Dystrophy, Patterned, 1 30 43.701
6
FND001 Fundus Albipunctatus 56 40.141
7
c RTN069 Retinitis Pigmentosa 7 44 38.858
8
c CHR449 Choroidal Dystrophy, Central Areolar 2 25 36.394
9
BTT011 Butterfly-Shaped Pigment Dystrophy 30 34.676
10
c MCL066 Macular Dystrophy, Vitelliform, 2 49 34.146
11
P STR022 Stargardt Disease 61 33.955
12
P CHR637 Choroidal Dystrophy, Central Areolar, 1 49 30.011
13
P VTL001 Vitelliform Macular Dystrophy 46 29.384
14
FND002 Fundus Dystrophy 54 28.866
15
PTT063 Pattern Dystrophy 36 26.738
16
P CND005 Cone Dystrophy 47 21.840
17
RTN023 Retinitis 45 19.765
18
DYN002 Doyne Honeycomb Retinal Dystrophy 44 17.753
19
CHR081 Choroideremia 58 17.595
20
P RTN016 Retinal Degeneration 52 17.316
21
ISL145 Isolated Macular Dystrophy 23 15.321
23
c CNR007 Cone-Rod Dystrophy 6 53 14.765
24
P RTN018 Retinal Disease 53 13.927
25
BST008 Bestrophinopathy, Autosomal Recessive 47 12.518
26
LBR036 Leber Plus Disease 67 11.086
27
LTN004 Late-Onset Retinal Degeneration 59 10.819
28
P USH001 Usher Syndrome 63 10.306
29
P NGH001 Night Blindness 52 9.598
30
c RTN172 Retinitis Pigmentosa 1 45 9.398
31
c AMY091 Amyotrophic Lateral Sclerosis 1 87 9.125
32
DGN006 Digenic Disease 26 9.125
33
PRP026 Peripheral Retinal Degeneration 29 9.125
34
FML292 Familial Drusen 34 8.312
35
STR046 Stargardt Macular Degeneration 27 8.038
36
MLT117 Multifocal Pattern Dystrophy Simulating Fundus Flavimaculatus 9 7.979
37
c USH035 Usher Syndrome Type 2 51 7.605
38
HRD016 Hereditary Retinal Dystrophy 33 7.574
39
P EYD002 Eye Disease 57 6.898
40
c LBR004 Leber Congenital Amaurosis 1 53 6.675
41
P CNG010 Congenital Stationary Night Blindness 56 6.610
42
P ACH003 Achromatopsia 61 6.610
43
c NNN011 Noonan Syndrome 4 47 6.453
44
c RTN054 Retinitis Pigmentosa 25 43 6.453
45
NWF001 Newfoundland Rod-Cone Dystrophy 36 6.453
46
c EXD006 Exudative Vitreoretinopathy 5 41 6.453
47
OCC002 Occult Macular Dystrophy 46 6.453
48
P SNR003 Senior-Loken Syndrome 1 58 6.453
49
VTR010 Vitreoretinochoroidopathy 49 6.453
50
GYR004 Gyrate Atrophy of Choroid and Retina 58 6.453
51
P NNP021 Nanophthalmos 40 6.453
52
DGN003 Degeneration of Macula and Posterior Pole 29 6.453
53
P BRD002 Bardet-Biedl Syndrome 66 6.453
54
RSP023 Rasopathy 54 6.453
55
EGD001 Ego-Dystonic Sexual Orientation 8 6.453
56
CHR079 Choroid Disease 37 6.453
57
GND002 Gender Identity Disorder 40 6.453
58
PRT032 Partial Central Choroid Dystrophy 21 6.453
59
HRD019 Hereditary Choroidal Atrophy 24 6.453
60
EYD001 Eye Degenerative Disease 27 6.453
61
NRR001 Neuroretinitis 42 5.336
62
c INH030 Inherited Retinal Disorder 28 2.077
63
P PRS040 Prostate Cancer 95 1.342
64
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.281
65
c RTN064 Retinitis Pigmentosa 35 35 1.208
66
RTN187 Retinitis Pigmentosa-Deafness Syndrome 48 1.088
67
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.051
68
c USH036 Usher Syndrome, Type I 60 1.051
69
P SNS001 Sensorineural Hearing Loss 60 1.051
70
P LBR033 Leber Congenital Amaurosis / Early-Onset Severe Retinal Dystrophy 23 1.008
71
c CHR665 Choroidal Dystrophy, Central Areolar, 3 15 0.893
72
P OVR042 Ovarian Cancer 88 0.551
73
P BRS047 Breast Cancer 97 0.551
74
P PNC035 Pancreatic Cancer 87 0.551
75
CLL010 Cellular Ependymoma 58 0.551
76
IRN008 Iron Overload in Africa 50 0.418
77
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 0.418
78
c HPT073 Hepatitis C Virus 70 0.418
79
RJS001 Ruijs-Aalfs Syndrome 47 0.418
80
P HPT023 Hepatocellular Carcinoma 95 0.418
81
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.418
82
ADL096 Adult Hepatocellular Carcinoma 60 0.418
83
HPT079 Hepatoid Adenocarcinoma 39 0.418
84
PDT042 Pediatric Hepatocellular Carcinoma 51 0.418
85
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.418
86
FBR086 Fibrolamellar Carcinoma 59 0.418
87
HPT011 Hepatocellular Clear Cell Carcinoma 46 0.418
88
PTY007 Pityriasis Rotunda 27 0.418
89
P MYP006 Myopia 55 0.417
90
PTH003 Pathologic Nystagmus 52 0.352
91
SRS007 Sorsby Fundus Dystrophy 51 0.315
92
c RTN048 Retinitis Pigmentosa 19 39 0.315
93
c MCL073 Macular Dystrophy, Vitelliform, 1 21 0.315
94
c CNR005 Cone-Rod Dystrophy 3 40 0.315
95
c MCL061 Macular Dystrophy, Vitelliform, 4 21 0.315
96
c MCL056 Macular Dystrophy, Vitelliform, 5 21 0.315
97
c USH037 Usher Syndrome, Type Iia 50 0.273
98
c RTN116 Retinitis Pigmentosa 56 25 0.273
99
c RTN141 Retinitis Pigmentosa 39 44 0.273
100
c DWL002 Dowling-Degos Disease 1 58 0.223
101
P PSD087 Pseudoxanthoma Elasticum 66 0.223
102
c RTN047 Retinitis Pigmentosa 18 45 0.223
103
c LBR018 Leber Congenital Amaurosis 8 47 0.223
104
c OPT053 Optic Atrophy 1 62 0.223
105
c RTN043 Retinitis Pigmentosa 13 43 0.223
106
c RTN042 Retinitis Pigmentosa 12 42 0.223
107
c RTN041 Retinitis Pigmentosa 11 43 0.223
108
RTN017 Retinal Detachment 60 0.157
109
ALS001 Alstrom Syndrome 65 0.157
110
c RTN150 Retinitis Pigmentosa 10 44 0.157
111
P MCK013 Meckel Syndrome, Type 1 64 0.157
112
IFP003 Ifap Syndrome 2 41 0.157
113
RTN203 Retinal Dystrophy, Reticular Pigmentary, of Posterior Pole 11 0.157
114
c HRM005 Hermansky-Pudlak Syndrome 1 55 0.157
115
P JBR020 Joubert Syndrome 1 74 0.157
116
c BRD010 Bardet-Biedl Syndrome 1 64 0.157
117
c SPN101 Spinocerebellar Ataxia 29 58 0.157
118
c NPH019 Nephronophthisis 1 50 0.157
119
LBR038 Leber Hereditary Optic Neuropathy, Modifier of 62 0.157
120
c LBR008 Leber Congenital Amaurosis 13 41 0.157
121
c MCR115 Microvascular Complications of Diabetes 5 65 0.157
122
PRL047 Prolonged Electroretinal Response Suppression 43 0.157
123
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.157
124
c LBR017 Leber Congenital Amaurosis 7 38 0.157
125
c LBR013 Leber Congenital Amaurosis 3 46 0.157
126
c WLF013 Wolfram Syndrome 1 60 0.157
127
P LNG064 Lung Cancer Susceptibility 3 69 0.157
128
P OPT006 Optic Nerve Disease 57 0.157
129
P NPH005 Nephronophthisis 59 0.157
130
SCT002 Scotoma 42 0.157
131
CNT060 Central Serous Chorioretinopathy 38 0.157
132
RFR003 Refractive Error 41 0.157
133
c JVN041 Juvenile Nephronophthisis 45 0.157
134
P HRD217 Hereditary Optic Neuropathy 36 0.157
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