Search results for sag

86 hits were found for sag

# Family MCID Name MIFTS Score
1
c SGR002 Sag-Related Retinitis Pigmentosa 9 9.395
2
P NGH001 Night Blindness 48 4.286
3
P OGC003 Oguchi Disease-1 17 4.175
4
c HRD015 Hereditary Night Blindness 36 4.130
5
P RTN008 Retinitis Pigmentosa 80 3.963
6
P UVT001 Uveitis 58 3.912
7
RTN001 Retinal Vasculitis 44 3.912
8
c RTN143 Retinitis Pigmentosa 47 40 3.623
9
BHC003 Behcet Syndrome 60 3.499
10
P FND001 Fundus Albipunctatus 55 3.499
11
P RTN016 Retinal Degeneration 54 3.499
12
ELS001 Eales Disease 47 3.499
13
c PST005 Posterior Uveitis 46 3.499
14
P PNB001 Pineoblastoma 44 3.499
15
CHR078 Chorioretinitis 40 3.499
16
P CNG010 Congenital Stationary Night Blindness 53 3.279
17
RTN018 Retinal Disease 53 3.030
18
P PNV001 Panuveitis 50 3.030
19
PNC056 Pineocytoma 39 3.030
20
MDL003 Medullomyoblastoma 35 3.030
21
CRB030 Cerebellum Cancer 35 3.030
22
CNC014 Cancer-Associated Retinopathy 34 3.030
23
CRB022 Cerebellar Liponeurocytoma 33 3.030
24
PNL014 Pineal Gland Cancer 32 3.030
25
PPL013 Papillary Ependymoma 31 3.030
26
PNL002 Pineal Parenchymal Tumor of Intermediate Differentiation 30 3.030
27
PNP001 Panophthalmitis 24 3.030
28
ACT120 Acute Zonal Occult Outer Retinopathy 23 3.030
29
MLN046 Melanoma-Associated Retinopathy 22 3.030
30
PRL018 Purulent Endophthalmitis 19 3.030
31
FCL013 Focal Chorioretinitis 15 3.030
32
c BRD017 Bardet-Biedl Syndrome 5 39 2.474
33
c RTN147 Retinitis Pigmentosa 48 32 2.474
34
INT003 Intracranial Hypotension 34 0.138
35
ACH004 Achondroplasia 66 0.087
36
P STR020 Strabismus 51 0.087
37
SPN340 Spontaneous Intracranial Hypotension 26 0.087
38
P NRB001 Neuroblastoma 70 0.062
39
TST021 Testicular Germ Cell Tumor 69 0.062
40
P HPT021 Hepatitis 69 0.062
41
DWN001 Down Syndrome 66 0.062
42
P KDN017 Kidney Cancer 65 0.062
43
DMN002 Dementia 65 0.062
44
c HPT016 Hepatitis B 64 0.062
45
MNK001 Menkes Disease 60 0.062
46
c VRL010 Viral Hepatitis 60 0.062
47
c HPT003 Hepatitis a 59 0.062
48
P CTS001 Cutis Laxa 58 0.062
49
P PLY006 Polydactyly 56 0.062
50
c HPT007 Hepatitis E 54 0.062
51
TST014 Testicular Cancer 53 0.062
52
HYP080 Hypogonadism 53 0.062
53
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.062
54
P GND004 Gonadal Dysgenesis 51 0.062
55
HYP005 Hypokalemia 51 0.062
56
HND003 Hand-Foot-Uterus Syndrome 50 0.062
57
RTN023 Retinitis 50 0.062
58
END035 Endocrine Gland Cancer 49 0.062
59
c NGH019 Night Blindness, Congenital Stationary , 1a, X-Linked 45 0.062
60
SMN007 Seminoma 45 0.062
61
OCC006 Occipital Horn Syndrome 44 0.062
62
CRD118 Cardiovascular Cancer 44 0.062
63
TST015 Testicular Disease 44 0.062
64
MLR006 Male Reproductive Organ Cancer 43 0.062
65
SXL003 Sexual Disorder 42 0.062
66
RPR002 Reproductive System Disease 41 0.062
67
P TST026 Testicular Germ Cell Cancer 39 0.062
68
GND003 Gonadal Disease 39 0.062
69
SXD001 Sex Differentiation Disease 38 0.062
70
HYP064 Hypogonadotropism 37 0.062
71
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.062
72
c BRN108 Branchiootic Syndrome 1 34 0.062
73
IMP003 Impaired Renal Function Disease 34 0.062
74
MLR007 Male Reproductive System Disease 34 0.062
75
NNS011 Nonseminomatous Germ Cell Tumor 33 0.062
76
WRN004 Wrinkly Skin Syndrome 32 0.062
77
TST043 Testicular Seminoma 30 0.062
78
MCR095 Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis 28 0.062
79
DBR002 De Barsy Syndrome 28 0.062
80
ENP001 Enophthalmos 28 0.062
81
HRN022 Hearing Loss/deafness 26 0.062
82
YNG002 Young Syndrome 26 0.062
83
GRM003 German Syndrome 22 0.062
84
HPD002 Hepadnavirus Infection 22 0.062
85
c FML249 Familial Amyloidosis, Finnish Type 19 0.062
86
TST041 Testicular Germ Cell Tumor Non-Seminomatous 11 0.062
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