Search results for frzb

128 hits were found for frzb

# Family MCID Name MIFTS Score
1
OST012 Osteoarthritis 77 36.946
2
P HPT023 Hepatocellular Carcinoma 95 16.678
3
P RTN016 Retinal Degeneration 52 13.432
4
OST159 Osteogenic Sarcoma 66 13.092
5
P OST002 Osteoporosis 77 11.969
6
MCR013 Microphthalmia 60 10.967
7
P SCL048 Sclerosteosis 58 8.381
8
HLZ001 Holzgreve Syndrome 37 7.755
9
P NNP021 Nanophthalmos 40 7.755
10
P VNB005 Van Buchem Disease 58 7.755
11
c DVL040 Developmental and Epileptic Encephalopathy 12 37 7.755
12
P EXD001 Exudative Vitreoretinopathy 55 7.755
13
P CRN015 Cornelia De Lange Syndrome 67 7.755
14
LCL004 Localized Osteosarcoma 34 7.755
15
EXD009 Exudative Vitreoretinopathy 2, X-Linked 39 7.755
16
P LPS002 Liposarcoma 64 1.736
17
BNR002 Bone Resorption Disease 47 1.671
18
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.613
19
P MSC005 Muscular Dystrophy 66 1.401
20
P LMB006 Limb-Girdle Muscular Dystrophy 52 1.401
21
P GST053 Gastric Cancer 82 1.365
22
P CHN012 Chondrosarcoma 56 1.265
23
SRC014 Sarcoma 64 1.242
24
SPN035 Spindle Cell Sarcoma 51 1.242
25
MSC007 Muscle Hypertrophy 64 1.219
26
P FBR017 Fibrosarcoma 55 1.219
27
SFT003 Soft Tissue Sarcoma 57 1.219
28
c PCH010 Pachyonychia Congenita 3 43 1.194
29
RPD005 Rapidly Involuting Congenital Hemangioma 48 1.194
30
P MYP004 Myopathy 67 1.141
31
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 1.111
32
c AMY091 Amyotrophic Lateral Sclerosis 1 88 1.111
33
P LTR001 Lateral Sclerosis 58 1.111
34
ART016 Aortic Aneurysm 69 1.111
35
ANR040 Aneurysm 60 1.111
36
P MSC003 Muscular Atrophy 52 1.078
37
CLR108 Colorectal Adenoma 63 1.042
38
ADN018 Adenoma 58 1.042
39
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.002
40
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.002
41
P PNC035 Pancreatic Cancer 86 0.883
42
P RHM011 Rheumatoid Arthritis 81 0.739
43
P BRS047 Breast Cancer 97 0.731
44
P PRS040 Prostate Cancer 95 0.517
45
P OVR042 Ovarian Cancer 88 0.517
46
P LNG032 Lung Cancer 98 0.517
47
c NRB010 Neuroblastoma 1 60 0.431
48
CTN007 Cutaneous Leishmaniasis 61 0.431
49
EXS001 Exostosis 49 0.402
50
P PLM036 Pulmonary Fibrosis 65 0.402
51
MYL069 Myeloma, Multiple 77 0.372
52
SYN007 Synovitis 54 0.372
53
PLC002 Plica Syndrome 35 0.372
54
c LKM063 Leukemia, Chronic Myeloid 71 0.263
55
KSH004 Kashin-Beck Disease 37 0.263
56
SVR004 Severe Combined Immunodeficiency 71 0.263
57
P LKM002 Leukemia 66 0.263
58
HYP266 Hypoxia 56 0.263
59
PLS016 Plasma Cell Leukemia 53 0.263
60
c SPN225 Spondyloarthropathy 1 70 0.215
61
P FBR025 Fibrochondrogenesis 55 0.215
62
PSR001 Psoriatic Arthritis 61 0.215
63
CLF027 Cleft Palate, Isolated 64 0.215
64
GLS018 Glass Syndrome 60 0.215
65
SPN051 Spondylitis 51 0.215
66
P RCT021 Rectum Cancer 54 0.215
67
INF009 Inflammatory Spondylopathy 30 0.215
68
P ART023 Arthropathy 60 0.215
69
PLS037 Plasma Cell Tumor 20 0.215
70
P ALZ034 Alzheimer Disease 87 0.152
71
P BLD134 Bladder Cancer 79 0.152
72
P RTN024 Retinoblastoma 72 0.152
73
c MSC169 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 1 61 0.152
74
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.152
75
DWN001 Down Syndrome 70 0.152
76
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.152
77
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.152
78
MYL009 Myelodysplastic Syndrome 67 0.152
79
INT395 Intracranial Meningioma 48 0.152
80
P MLT020 Multiple Sclerosis 79 0.152
81
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.152
82
P HYP760 Hypothyroidism, Congenital, Nongoitrous, 2 54 0.152
83
RNL077 Renal Fibrosis 46 0.152
84
P FML011 Familial Adenomatous Polyposis 71 0.152
85
c CNG006 Congenital Hypothyroidism 63 0.152
86
FBR054 Fibroma 44 0.152
87
CHR612 Chromosome 15q14 Deletion Syndrome 19 0.152
88
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.152
89
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.152
90
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.152
91
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.152
92
c HPT073 Hepatitis C Virus 71 0.152
93
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.152
94
HYP748 Hypertelorism 46 0.152
95
P CLR023 Colorectal Cancer 100 0.152
96
APR006 Apert Syndrome 69 0.152
97
c SCL052 Scleroderma, Familial Progressive 60 0.152
98
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.152
99
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.152
100
P ATR001 Atrioventricular Septal Defect 55 0.152
101
c ATR047 Atrioventricular Septal Defect 2 26 0.152
102
CHR619 Chromosome 2q35 Duplication Syndrome 64 0.152
103
P TTR001 Tetralogy of Fallot 69 0.152
104
OST017 Osteomyelitis 63 0.152
105
P ORF002 Orofacial Cleft 42 0.152
106
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.152
107
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.152
108
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 49 0.152
109
DFC004 Deficiency Anemia 74 0.152
110
P SBS003 Substance Abuse 54 0.152
111
c HPT001 Hepatitis C 61 0.152
112
IRN002 Iron Metabolism Disease 56 0.152
113
c BSL007 Basal Cell Carcinoma 68 0.152
114
P CRN037 Craniosynostosis 67 0.152
115
P HYP086 Hypothyroidism 69 0.152
116
P OSS001 Ossifying Fibroma 42 0.152
117
IRN001 Iron Deficiency Anemia 58 0.152
118
INT066 Interstitial Lung Disease 60 0.152
119
EMB004 Embryonal Carcinoma 55 0.152
120
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.152
121
MNN043 Meningioma, Familial 79 0.152
122
OST016 Osteochondrosis 52 0.152
123
LNG099 Lung Disease 62 0.152
124
SCR001 Secretory Meningioma 40 0.152
125
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.152
126
CHR178 Chromosomal Triplication 34 0.152
127
DFF035 Diffuse Cutaneous Systemic Sclerosis 45 0.152
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