Search results for FK 506

117 hits were found for FK 506

# Family MCID Name MIFTS Score
1
P GRF003 Graft-Versus-Host Disease 72 0.208
2
CYT002 Cytokine Deficiency 42 0.166
3
P PSR002 Psoriasis 62 0.154
4
P LYM033 Lymphoproliferative Syndrome 59 0.154
5
P TRM003 Tremor 54 0.154
6
P HML001 Hemolytic-Uremic Syndrome 53 0.154
7
PST011 Pustulosis of Palm and Sole 52 0.154
8
P NPH012 Nephrotic Syndrome 60 0.147
9
ATM095 Autoimmune Disease 62 0.140
10
ISC004 Ischemia 58 0.140
11
P GLM007 Glomerulonephritis 57 0.140
12
PYD001 Pyoderma Gangrenosum 54 0.125
13
PYD002 Pyoderma 50 0.125
14
ALL014 Allergic Encephalomyelitis 38 0.125
15
P VSC011 Vasculitis 62 0.109
16
c ACT135 Acute Graft Versus Host Disease 52 0.109
17
OCL069 Ocular Motor Apraxia 51 0.109
18
c ATM045 Autoimmune Glomerulonephritis 36 0.109
19
c HYP836 Hypercholesterolemia, Familial, 1 73 0.089
20
ULC004 Ulcerative Colitis 73 0.089
21
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.089
22
c HPT073 Hepatitis C Virus 72 0.089
23
P THR014 Thrombocytopenia 67 0.089
24
P DRM053 Dermatitis, Atopic 66 0.089
25
CLT003 Colitis 62 0.089
26
c HPT001 Hepatitis C 62 0.089
27
LPP008 Lipoprotein Quantitative Trait Locus 62 0.089
28
CHL068 Cholestasis 61 0.089
29
P MYC008 Myocarditis 59 0.089
30
BRN002 Bronchiolitis 59 0.089
31
P UVT001 Uveitis 57 0.089
32
P PYL005 Pyelonephritis 56 0.089
33
c ACT134 Acute Liver Failure 56 0.089
34
BRN012 Bronchiolitis Obliterans 55 0.089
35
P ART021 Arteriosclerosis 54 0.089
36
PST046 Post-Transplant Lymphoproliferative Disease 53 0.089
37
CYT005 Cytomegalovirus Retinitis 50 0.089
38
RTN023 Retinitis 46 0.089
39
NRR001 Neuroretinitis 42 0.089
40
PRS063 Paresthesia 41 0.089
41
WLL004 Wallerian Degeneration 39 0.089
42
P ASP006 Aspergillosis 69 0.086
43
PRT018 Portal Vein Thrombosis 50 0.085
44
CRH001 Crohn's Disease 74 0.076
45
ALL026 Allergic Hypersensitivity Disease 62 0.076
46
HYP066 Hyperglycemia 61 0.076
47
PRT013 Portal Hypertension 59 0.076
48
ADN018 Adenoma 59 0.076
49
P ALP008 Alopecia 54 0.076
50
P PNC044 Pancreatitis 61 0.075
51
c ACT027 Acute Pancreatitis 60 0.075
52
c CHL119 Cholangitis, Primary Sclerosing 57 0.075
53
P CHL066 Cholangitis 51 0.075
54
P MMB011 Membranous Nephropathy 50 0.075
55
P SCL009 Sclerosing Cholangitis 48 0.075
56
c SYS001 Systemic Lupus Erythematosus 86 0.063
57
STR067 Stroke, Ischemic 81 0.063
58
GLB015 Glioblastoma Multiforme 75 0.063
59
P RSP003 Respiratory Failure 74 0.063
60
HMN044 Human Immunodeficiency Virus Type 1 71 0.063
61
P MYS003 Myasthenia Gravis 68 0.063
62
P HPT021 Hepatitis 67 0.063
63
P HYP098 Hypereosinophilic Syndrome 67 0.063
64
P PLM037 Pulmonary Hypertension 67 0.063
65
P ART005 Arteriovenous Malformation 65 0.063
66
c DBT099 Diabetes Mellitus, Type I 65 0.063
67
ANG020 Angiosarcoma 64 0.063
68
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.063
69
P HML002 Hemolytic Anemia 63 0.063
70
P NTR004 Neutropenia 63 0.063
71
SKN016 Skin Disease 63 0.063
72
c ACT068 Acute Cystitis 63 0.063
73
TRN015 Transient Cerebral Ischemia 63 0.063
74
BLL006 Bullous Pemphigoid 62 0.063
75
HSH003 Hashimoto Thyroiditis 62 0.063
76
TXC005 Toxic Shock Syndrome 62 0.063
77
LVR012 Liver Cirrhosis 62 0.063
78
DRM006 Dermatitis 61 0.063
79
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.063
80
P LPS004 Lupus Erythematosus 61 0.063
81
SPN186 Spinal Cord Injury 60 0.063
82
LNG099 Lung Disease 60 0.063
83
P ALP009 Alopecia Areata 60 0.063
84
P CTR002 Cataract 60 0.063
85
CHL123 Chlamydia 59 0.063
86
P NPH005 Nephronophthisis 59 0.063
87
CNT047 Contact Dermatitis 58 0.063
88
c CHR417 Chronic Graft Versus Host Disease 57 0.063
89
APH002 Aphasia 57 0.063
90
ALL010 Allergic Contact Dermatitis 56 0.063
91
P PLY019 Polyneuropathy 56 0.063
92
P PTT006 Pituitary Adenoma 55 0.063
93
OCL020 Ocular Cicatricial Pemphigoid 55 0.063
94
P STR020 Strabismus 55 0.063
95
PRP030 Purpura 54 0.063
96
GLC003 Glucose Intolerance 54 0.063
97
P PTS002 Ptosis 53 0.063
98
IMP005 Impotence 52 0.063
99
ART140 Arteries, Anomalies of 52 0.063
100
P THY032 Thyroiditis 52 0.063
101
CCT002 Cicatricial Pemphigoid 51 0.063
102
BLP005 Blepharitis 50 0.063
103
FSC004 Fasciitis 50 0.063
104
CGN006 Cogan Syndrome 48 0.063
105
NCR007 Necrotizing Fasciitis 48 0.063
106
P RNL015 Renal Hypertension 47 0.063
107
CNT025 Central Pontine Myelinolysis 46 0.063
108
SBC016 Subacute Delirium 44 0.063
109
SCT002 Scotoma 44 0.063
110
MCH006 Mechanical Strabismus 42 0.063
111
PLM052 Pulmonary Arteriovenous Malformation 39 0.063
112
LYM052 Lymphomatoid Papulosis 38 0.063
113
STR077 Streptococcal Toxic-Shock Syndrome 37 0.063
114
HYP026 Hypoglycemic Coma 36 0.063
115
CHR178 Chromosomal Triplication 35 0.063
116
PLM151 Pulmonary Arteriovenous Fistulas 34 0.063
117
HML018 Homologous Wasting Disease 22 0.063
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