Search results for sag

82 hits were found for sag

# Family MCID Name MIFTS Score
1
c SGR002 Sag-Related Retinitis Pigmentosa 8 7.535
2
P NGH001 Night Blindness 47 4.269
3
c HRD015 Hereditary Night Blindness 28 4.179
4
P CNG010 Congenital Stationary Night Blindness 53 4.135
5
P RTN008 Retinitis Pigmentosa 80 3.972
6
c RTN143 Retinitis Pigmentosa 47 40 3.612
7
P UVT001 Uveitis 57 3.486
8
RTN001 Retinal Vasculitis 43 3.486
9
P OGC003 Oguchi Disease-1 18 3.320
10
BHC003 Behcet Syndrome 62 3.019
11
P FND001 Fundus Albipunctatus 55 3.019
12
P RTN016 Retinal Degeneration 53 3.019
13
ELS001 Eales Disease 46 3.019
14
P PNB001 Pineoblastoma 46 3.019
15
c PST005 Posterior Uveitis 45 3.019
16
CHR078 Chorioretinitis 37 3.019
17
WHM001 Whim Syndrome 52 2.465
18
ART002 Arts Syndrome 52 2.465
19
RTN018 Retinal Disease 51 2.465
20
P PNV001 Panuveitis 48 2.465
21
c BRD017 Bardet-Biedl Syndrome 5 41 2.465
22
PNC056 Pineocytoma 39 2.465
23
MDL003 Medullomyoblastoma 35 2.465
24
CNC014 Cancer-Associated Retinopathy 33 2.465
25
c RTN147 Retinitis Pigmentosa 48 33 2.465
26
PNL014 Pineal Gland Cancer 33 2.465
27
CRB022 Cerebellar Liponeurocytoma 32 2.465
28
PPL013 Papillary Ependymoma 32 2.465
29
PNL002 Pineal Parenchymal Tumor of Intermediate Differentiation 30 2.465
30
PNP001 Panophthalmitis 23 2.465
31
ACT120 Acute Zonal Occult Outer Retinopathy 23 2.465
32
MLN046 Melanoma-Associated Retinopathy 22 2.465
33
PRL018 Purulent Endophthalmitis 19 2.465
34
FCL013 Focal Chorioretinitis 15 2.465
35
INT003 Intracranial Hypotension 33 0.141
36
ACH004 Achondroplasia 66 0.089
37
MNK001 Menkes Disease 63 0.089
38
P STR020 Strabismus 52 0.089
39
RTN023 Retinitis 49 0.089
40
WRN004 Wrinkly Skin Syndrome 34 0.089
41
SPN340 Spontaneous Intracranial Hypotension 25 0.089
42
P LVR013 Liver Disease 72 0.063
43
P NRB001 Neuroblastoma 71 0.063
44
DWN001 Down Syndrome 69 0.063
45
P HPT021 Hepatitis 68 0.063
46
TST021 Testicular Germ Cell Tumor 67 0.063
47
c HPT016 Hepatitis B 62 0.063
48
P CTS001 Cutis Laxa 60 0.063
49
c HPT003 Hepatitis a 56 0.063
50
P PLY006 Polydactyly 54 0.063
51
HYP080 Hypogonadism 52 0.063
52
TST014 Testicular Cancer 52 0.063
53
DMN002 Dementia 52 0.063
54
c HPT007 Hepatitis E 51 0.063
55
END035 Endocrine Gland Cancer 50 0.063
56
HYP005 Hypokalemia 50 0.063
57
OCC006 Occipital Horn Syndrome 47 0.063
58
CRD118 Cardiovascular Cancer 45 0.063
59
BRT030 Birth Defects 44 0.063
60
TST015 Testicular Disease 43 0.063
61
RPR002 Reproductive System Disease 43 0.063
62
SMN007 Seminoma 42 0.063
63
P TST026 Testicular Germ Cell Cancer 40 0.063
64
NCL006 Nicolaides-Baraitser Syndrome 40 0.063
65
GND003 Gonadal Disease 40 0.063
66
MLR007 Male Reproductive System Disease 36 0.063
67
c CTS030 Cutis Laxa, Autosomal Recessive, Type Ia 35 0.063
68
HYP064 Hypogonadotropism 35 0.063
69
TST043 Testicular Seminoma 34 0.063
70
c EHL027 Ehlers-Danlos Syndrome, Type Viic 34 0.063
71
P GRM010 Germ Cells Tumors 34 0.063
72
MCR095 Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis 31 0.063
73
DBR002 De Barsy Syndrome 31 0.063
74
NNS011 Nonseminomatous Germ Cell Tumor 30 0.063
75
c CTS023 Cutis Laxa, Autosomal Recessive, Type Iib 30 0.063
76
YNG002 Young Syndrome 29 0.063
77
GRM003 German Syndrome 27 0.063
78
ENP001 Enophthalmos 27 0.063
79
c MNT295 Mental Retardation, X-Linked, Syndromic 33 24 0.063
80
HPD002 Hepadnavirus Infection 22 0.063
81
BLP041 Blepharochalasis and Double Lip 20 0.063
82
c FML249 Familial Amyloidosis, Finnish Type 19 0.063
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