Search results for srf

103 hits were found for srf

# Family MCID Name MIFTS Score
1
SKN016 Skin Disease 63 3.458
2
P RHM011 Rheumatoid Arthritis 80 3.428
3
LYM007 Lymphangioleiomyomatosis 69 3.428
4
c DLT002 Dilated Cardiomyopathy 79 2.940
5
MGK001 Megakaryocytic Leukemia 64 2.940
6
MYF001 Myofibroma 45 2.866
7
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 2.835
8
c AMY091 Amyotrophic Lateral Sclerosis 1 89 2.799
9
MLL002 Miller Fisher Syndrome 43 2.799
10
OCL052 Ocular Dominance 42 2.026
11
FMR011 Fumarate Hydratase Deficiency 30 2.026
12
MYP064 Myopericytoma 30 2.026
13
P NRN021 Neuronal Ceroid Lipofuscinosis 64 1.979
14
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 63 1.979
15
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 1.979
16
c CRD183 Ceroid Lipofuscinosis, Neuronal, 2 55 1.979
17
RHM014 Rheumatoid Vasculitis 37 1.979
18
MSC007 Muscle Hypertrophy 64 0.140
19
c PLM128 Pulmonary Hypertension, Primary, 2 29 0.128
20
c ACT073 Acute Leukemia 58 0.114
21
P HRT032 Heart Disease 75 0.099
22
P LKM002 Leukemia 68 0.099
23
P VSC007 Vascular Disease 63 0.099
24
c PCH010 Pachyonychia Congenita 3 44 0.099
25
P BRS047 Breast Cancer 97 0.081
26
P GST053 Gastric Cancer 83 0.081
27
c ATR087 Atrial Standstill 1 75 0.081
28
GST040 Gastric Adenocarcinoma 70 0.081
29
P SYS005 Systemic Scleroderma 68 0.081
30
c ATS007 Autism Spectrum Disorder 67 0.081
31
P GLM045 Glioma 63 0.081
32
P ATR010 Atrial Heart Septal Defect 60 0.081
33
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.081
34
c INT072 Intestinal Pseudo-Obstruction 56 0.081
35
HRT011 Heart Septal Defect 50 0.081
36
VCC001 Vaccinia 49 0.081
37
GLL048 Glial Tumor 45 0.081
38
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.081
39
P HPT023 Hepatocellular Carcinoma 100 0.057
40
ESP021 Esophageal Cancer 90 0.057
41
P ALZ034 Alzheimer Disease 88 0.057
43
STR067 Stroke, Ischemic 81 0.057
44
P RTT002 Rett Syndrome 80 0.057
45
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.057
46
P LNG064 Lung Cancer Susceptibility 3 78 0.057
47
SVR004 Severe Combined Immunodeficiency 73 0.057
48
ULC004 Ulcerative Colitis 73 0.057
49
c THR092 Thrombophilia Due to Thrombin Defect 73 0.057
50
P FRG001 Fragile X Syndrome 70 0.057
51
LKC009 Leukocyte Adhesion Deficiency, Type I 69 0.057
52
P MJR001 Major Depressive Disorder 68 0.057
53
P PLM037 Pulmonary Hypertension 67 0.057
54
OST159 Osteogenic Sarcoma 66 0.057
55
P DRM053 Dermatitis, Atopic 66 0.057
56
P PLM036 Pulmonary Fibrosis 65 0.057
57
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.057
58
NRR002 Norrie Disease 64 0.057
59
P FRD001 Friedreich Ataxia 64 0.057
60
P CRN300 Coronary Heart Disease 1 63 0.057
61
DPR016 Depression 63 0.057
63
P NPH012 Nephrotic Syndrome 60 0.057
64
ETN001 Eating Disorder 60 0.057
65
STT001 Status Epilepticus 60 0.057
66
c ALB021 Albinism, Oculocutaneous, Type Ii 59 0.057
67
P INT070 Intestinal Obstruction 58 0.057
68
CRD132 Cardiac Conduction Defect 58 0.057
69
EYD002 Eye Disease 58 0.057
70
MNT002 Mental Depression 58 0.057
71
P CRD246 Cardiovascular System Disease 57 0.057
72
VSC002 Vascular Dementia 57 0.057
73
LMY014 Leiomyoma, Uterine 56 0.057
74
ERY051 Erythroleukemia, Familial 56 0.057
75
SLC006 Silicosis 56 0.057
76
P SBS003 Substance Abuse 55 0.057
77
P RTN018 Retinal Disease 53 0.057
78
c MCR113 Microvascular Complications of Diabetes 3 52 0.057
79
P SML001 Small Cell Carcinoma 52 0.057
80
TLN003 Telangiectasis 52 0.057
81
LMY002 Leiomyoma 52 0.057
82
OCL069 Ocular Motor Apraxia 51 0.057
83
ILS001 Ileus 51 0.057
84
P OVR082 Overgrowth Syndrome 50 0.057
85
P TMP001 Temporal Lobe Epilepsy 50 0.057
86
NTR046 Neutrophil Migration 50 0.057
87
c 46X049 46,xy Sex Reversal 2 48 0.057
88
HLX001 Helix Syndrome 47 0.057
89
RNL077 Renal Fibrosis 47 0.057
90
c MCR120 Microvascular Complications of Diabetes 7 47 0.057
91
KHN001 Kuhnt-Junius Degeneration 47 0.057
92
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.057
93
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.057
94
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.057
95
CVD001 Covid-19 44 0.057
96
LMY003 Leiomyomatosis 43 0.057
97
CYT002 Cytokine Deficiency 42 0.057
98
FBR019 Fibromatosis 41 0.057
99
c MCR130 Microvascular Complications of Diabetes 6 41 0.057
100
c MCR133 Microvascular Complications of Diabetes 4 41 0.057
101
INT020 Intravenous Leiomyomatosis 36 0.057
102
c LKM005 Leukemia, T-Cell, Chronic 34 0.057
103
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.057
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