Search results for srf

92 hits were found for srf

# Family MCID Name MIFTS Score
1
P HRT032 Heart Disease 78 4.994
2
P TCL004 T-Cell Leukemia 48 3.846
3
LYM007 Lymphangioleiomyomatosis 67 3.814
4
MGK001 Megakaryocytic Leukemia 65 3.260
5
c DLT002 Dilated Cardiomyopathy 81 3.237
6
OCL052 Ocular Dominance 41 2.251
7
MYP064 Myopericytoma 31 2.251
8
FMR011 Fumarate Hydratase Deficiency 31 2.251
9
RHM014 Rheumatoid Vasculitis 38 2.202
10
RTR007 Retroperitoneal Leiomyosarcoma 35 2.202
11
MSC007 Muscle Hypertrophy 65 0.144
12
c PLM128 Pulmonary Hypertension, Primary, 2 29 0.132
13
c ACT073 Acute Leukemia 59 0.118
14
P LKM002 Leukemia 69 0.102
15
P VSC007 Vascular Disease 65 0.102
16
c HMP012 Hemophagocytic Lymphohistiocytosis, Familial, 2 47 0.102
17
c PCH010 Pachyonychia Congenita 3 43 0.102
18
P BRS047 Breast Cancer 99 0.083
19
P GST053 Gastric Cancer 85 0.083
20
c ATR087 Atrial Standstill 1 76 0.083
21
c ATS007 Autism Spectrum Disorder 69 0.083
22
P SYS005 Systemic Scleroderma 68 0.083
23
GST040 Gastric Adenocarcinoma 67 0.083
24
P GLM045 Glioma 64 0.083
25
c INT072 Intestinal Pseudo-Obstruction 55 0.083
26
VCC001 Vaccinia 50 0.083
27
GLL048 Glial Tumor 48 0.083
28
P HPT023 Hepatocellular Carcinoma 99 0.059
29
P ALZ034 Alzheimer Disease 90 0.059
30
ESP021 Esophageal Cancer 90 0.059
32
STR067 Stroke, Ischemic 82 0.059
33
P RTT002 Rett Syndrome 81 0.059
34
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.059
35
P LNG064 Lung Cancer Susceptibility 3 79 0.059
36
ULC004 Ulcerative Colitis 75 0.059
37
c THR092 Thrombophilia Due to Thrombin Defect 74 0.059
38
GLB002 Glioblastoma 74 0.059
39
SVR004 Severe Combined Immunodeficiency 74 0.059
40
CRB039 Cerebrovascular Disease 71 0.059
41
P PLM037 Pulmonary Hypertension 69 0.059
42
P MJR001 Major Depressive Disorder 69 0.059
43
P FRG001 Fragile X Syndrome 69 0.059
44
P DRM053 Dermatitis, Atopic 68 0.059
45
OST159 Osteogenic Sarcoma 67 0.059
46
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.059
47
P FRD012 Friedreich Ataxia 1 65 0.059
48
P NPH012 Nephrotic Syndrome 65 0.059
49
DPR016 Depression 64 0.059
50
LKC009 Leukocyte Adhesion Deficiency, Type I 64 0.059
51
SKN016 Skin Disease 64 0.059
52
NRR002 Norrie Disease 63 0.059
53
STT001 Status Epilepticus 61 0.059
54
ETN001 Eating Disorder 61 0.059
56
P ATR010 Atrial Heart Septal Defect 61 0.059
57
P CRD132 Cardiac Conduction Defect 61 0.059
58
GLB015 Glioblastoma Multiforme 60 0.059
59
MNT002 Mental Depression 60 0.059
60
P INT070 Intestinal Obstruction 60 0.059
61
c ALB021 Albinism, Oculocutaneous, Type Ii 59 0.059
62
EYD002 Eye Disease 59 0.059
63
ERY051 Erythroleukemia, Familial 58 0.059
64
AGN016 Aging 58 0.059
65
LMY014 Leiomyoma, Uterine 57 0.059
66
VSC002 Vascular Dementia 57 0.059
67
ENH001 Enhanced S-Cone Syndrome 56 0.059
68
P SBS003 Substance Abuse 56 0.059
69
P SML001 Small Cell Carcinoma 55 0.059
70
TLN003 Telangiectasis 53 0.059
71
P RTN018 Retinal Disease 53 0.059
72
P TMP001 Temporal Lobe Epilepsy 53 0.059
73
OCL069 Ocular Motor Apraxia 53 0.059
74
LMY002 Leiomyoma 52 0.059
75
HRT011 Heart Septal Defect 52 0.059
76
ILS001 Ileus 51 0.059
77
OVR082 Overgrowth Syndrome 51 0.059
78
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.059
79
c HMN021 Human T-Cell Leukemia Virus Type 1 50 0.059
80
NTR046 Neutrophil Migration 49 0.059
81
FBR019 Fibromatosis 47 0.059
82
CYT002 Cytokine Deficiency 46 0.059
83
HLX001 Helix Syndrome 46 0.059
84
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.059
85
KHN001 Kuhnt-Junius Degeneration 45 0.059
86
LMY003 Leiomyomatosis 43 0.059
87
MYF001 Myofibroma 40 0.059
88
c LKM005 Leukemia, T-Cell, Chronic 35 0.059
89
INT020 Intravenous Leiomyomatosis 35 0.059
90
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.059
91
c 46X049 46,xy Sex Reversal 2 33 0.059
92
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.059
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