Search results for rax

96 hits were found for rax

# Family MCID Name MIFTS Score
1
c MCR114 Microphthalmia, Isolated 3 41 50.404
2
MCR013 Microphthalmia 60 48.973
3
CLB026 Colobomatous Microphthalmia 46 12.906
4
P SCL047 Sclerocornea 32 12.417
5
P LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 52 10.881
6
CLB010 Coloboma of Macula 53 9.230
7
P ISL020 Isolated Microphthalmia 23 7.919
8
c MCR252 Microphthalmia, Syndromic 5 38 7.853
9
c MCR245 Microphthalmia, Syndromic 8 46 7.694
10
c AXN009 Axenfeld-Rieger Syndrome, Type 1 48 7.694
11
c MCR251 Microphthalmia, Syndromic 6 48 7.694
12
c MCR137 Microphthalmia, Isolated 2 44 7.694
13
c BRD014 Bardet-Biedl Syndrome 2 53 7.694
14
GLL028 Gillespie Syndrome 52 7.694
15
CRN007 Corneal Staphyloma 20 7.694
16
ORB007 Orbital Cyst 22 7.694
17
P AXN002 Axenfeld-Rieger Syndrome 62 7.694
18
FRY006 Fryns Microphthalmia Syndrome 52 3.489
19
MCR103 Microtia 40 1.509
20
P FTL001 Fetal Alcohol Syndrome 55 1.449
21
FTL006 Fetal Alcohol Spectrum Disorder 43 1.449
22
c MCR115 Microvascular Complications of Diabetes 5 65 1.322
23
PTT001 Pituitary Hypoplasia 34 1.322
24
CLF027 Cleft Palate, Isolated 64 1.226
25
CNG608 Congenital Hypopituitarism 29 1.226
26
CLF001 Cleft Lip 54 1.226
27
P HYP083 Hypopituitarism 52 1.226
28
P DBT005 Diabetes Insipidus 54 1.226
29
CLF004 Cleft Lip/palate 57 1.226
30
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.199
31
P FNC044 Fanconi Anemia, Complementation Group C 56 1.170
32
c FNC027 Fanconi Anemia, Complementation Group a 81 1.170
33
ALL029 Allergic Disease 61 1.170
34
STM007 Stomatitis 52 1.170
35
c MCR241 Microphthalmia, Syndromic 3 55 1.139
36
P PRK039 Parkinsonism 55 1.105
37
c DYS059 Dystonia 16 47 1.105
38
P DYS154 Dystonia 64 1.105
39
P RTN209 Retinoschisis 1, X-Linked, Juvenile 59 1.024
40
P NNP021 Nanophthalmos 40 1.024
41
P PRS040 Prostate Cancer 95 0.573
42
P BRS047 Breast Cancer 97 0.573
43
P PNC035 Pancreatic Cancer 86 0.573
44
ESP021 Esophageal Cancer 84 0.390
45
c HPT016 Hepatitis B 62 0.356
46
P HPT021 Hepatitis 68 0.356
47
SX2004 Sox2 Disorder 13 0.356
49
c ANT086 Anterior Segment Dysgenesis 2 47 0.276
50
c ANT077 Anterior Segment Dysgenesis 1 46 0.276
51
P ANT088 Anterior Segment Dysgenesis 53 0.276
52
c AXN010 Axenfeld-Rieger Syndrome, Type 3 47 0.276
53
P RTN016 Retinal Degeneration 52 0.276
55
P CNR004 Cone-Rod Dystrophy 2 75 0.225
56
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.225
57
c CNR012 Cone-Rod Dystrophy 11 27 0.225
59
P RTN018 Retinal Disease 53 0.225
60
KRT002 Keratomalacia 54 0.225
61
CNG067 Congenital Cystic Eye 14 0.225
62
CRY010 Cryptophthalmos 25 0.225
63
P RTN024 Retinoblastoma 72 0.159
64
P RTN008 Retinitis Pigmentosa 79 0.159
65
c MCR261 Microphthalmia, Syndromic 2 50 0.159
66
NRR001 Neuroretinitis 42 0.159
67
P MLN069 Melanoma, Uveal 59 0.159
68
P ANR048 Aniridia 1 66 0.159
69
RTN017 Retinal Detachment 60 0.159
70
P CRD119 Cardiac Arrest 68 0.159
71
PNB004 Panbronchiolitis, Diffuse 34 0.159
72
PPL052 Papillomatosis, Confluent and Reticulated 34 0.159
73
ULN003 Ulnar-Mammary Syndrome 56 0.159
74
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 68 0.159
75
P ASP006 Aspergillosis 71 0.159
76
c ACT073 Acute Leukemia 59 0.159
77
BRN012 Bronchiolitis Obliterans 56 0.159
78
BRN002 Bronchiolitis 57 0.159
79
OVR063 Overnutrition 42 0.159
80
P MCR010 Microcephaly 59 0.159
81
PNM008 Pneumothorax 54 0.159
82
P AGM001 Agammaglobulinemia 67 0.159
83
RTN023 Retinitis 45 0.159
84
VCC001 Vaccinia 49 0.159
85
c MCR263 Microphthalmia, Syndromic 1 47 0.159
86
c MCR256 Microphthalmia, Syndromic 9 61 0.159
87
STN013 Stenotrophomonas Maltophilia Infection 26 0.159
88
P CTR002 Cataract 59 0.159
89
VRL011 Viral Infectious Disease 60 0.159
90
P PNM007 Pneumonia 64 0.159
91
P RBL001 Rubella 58 0.159
92
FND002 Fundus Dystrophy 55 0.159
93
P MSC005 Muscular Dystrophy 66 0.159
94
CNG124 Congenital Rubella 43 0.159
95
BRN101 Bronchiolitis Obliterans with Obstructive Pulmonary Disease 27 0.159
96
c INH030 Inherited Retinal Disorder 28 0.159
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