Search results for hes1

111 hits were found for hes1

# Family MCID Name MIFTS Score
1
P MDL005 Medulloblastoma 78 4.516
2
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 49 2.647
3
P MTR004 Maturity-Onset Diabetes of the Young 66 2.538
4
CHR594 Chromosome 3q29 Deletion Syndrome 43 2.538
5
HLX001 Helix Syndrome 46 0.308
6
P CLR023 Colorectal Cancer 100 0.154
7
P LKM002 Leukemia 69 0.133
8
P ADN016 Adenocarcinoma 65 0.133
9
c LKM061 Leukemia, Acute Myeloid 84 0.122
10
c LKM063 Leukemia, Chronic Myeloid 74 0.122
11
P MYL006 Myeloid Leukemia 61 0.122
12
P PNC035 Pancreatic Cancer 86 0.109
13
GLB002 Glioblastoma 74 0.109
14
GLB015 Glioblastoma Multiforme 60 0.109
15
P TCL004 T-Cell Leukemia 48 0.109
16
P GST053 Gastric Cancer 85 0.094
17
BRN028 Brain Cancer 75 0.094
18
P RTN024 Retinoblastoma 74 0.094
19
P LKM062 Leukemia, Acute Lymphoblastic 68 0.094
20
P GLM045 Glioma 64 0.094
21
ADN018 Adenoma 60 0.094
22
P LYM031 Lymphocytic Leukemia 56 0.094
23
c ACT020 Acute T Cell Leukemia 54 0.094
24
GLL048 Glial Tumor 48 0.094
25
c FML008 Familial Retinoblastoma 46 0.094
26
c LKM005 Leukemia, T-Cell, Chronic 35 0.094
27
c FNC027 Fanconi Anemia, Complementation Group a 81 0.077
28
CRV035 Cervical Cancer 77 0.077
29
DFC004 Deficiency Anemia 77 0.077
30
OST159 Osteogenic Sarcoma 67 0.077
31
SPN186 Spinal Cord Injury 63 0.077
32
c BRN108 Branchiootic Syndrome 1 62 0.077
33
SQM006 Squamous Cell Carcinoma 60 0.077
34
c ACT073 Acute Leukemia 59 0.077
35
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.077
36
ENH001 Enhanced S-Cone Syndrome 56 0.077
37
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.077
38
c FNC042 Fanconi Anemia, Complementation Group D2 56 0.077
39
TRM010 Traumatic Brain Injury 54 0.077
40
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.077
41
BLR001 Biliary Atresia 51 0.077
42
BRN071 Brain Injury 51 0.077
43
NRN001 Neuroendocrine Carcinoma 48 0.077
44
HRN029 Hearing Loss, Noise-Induced 38 0.077
45
ESP021 Esophageal Cancer 90 0.054
46
c SYS001 Systemic Lupus Erythematosus 88 0.054
47
P RTT002 Rett Syndrome 81 0.054
48
OST012 Osteoarthritis 80 0.054
49
P HRT032 Heart Disease 78 0.054
50
ULC004 Ulcerative Colitis 75 0.054
51
CRH001 Crohn's Disease 75 0.054
52
END057 Endometrial Cancer 74 0.054
53
SVR004 Severe Combined Immunodeficiency 74 0.054
54
P HNT016 Huntington Disease 72 0.054
55
ADN011 Adenoid Cystic Carcinoma 71 0.054
56
DWN001 Down Syndrome 70 0.054
57
MLN008 Melanoma 68 0.054
58
P NSP012 Nasopharyngeal Carcinoma 67 0.054
59
P HYP098 Hypereosinophilic Syndrome 67 0.054
60
SRC014 Sarcoma 67 0.054
61
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.054
62
CLN015 Colon Adenocarcinoma 65 0.054
63
LPD008 Lipid Metabolism Disorder 64 0.054
64
c GLC092 Glaucoma, Primary Open Angle 63 0.054
65
BRS099 Breast Ductal Carcinoma 63 0.054
66
FTT001 Fatty Liver Disease 63 0.054
67
MDD011 Mood Disorder 62 0.054
68
MCR013 Microphthalmia 62 0.054
69
ATM095 Autoimmune Disease 62 0.054
70
P VNT002 Ventricular Septal Defect 61 0.054
71
P BPL003 Bipolar Disorder 59 0.054
72
CYT008 Cytomegalovirus Infection 58 0.054
73
HYP266 Hypoxia 58 0.054
74
ERY051 Erythroleukemia, Familial 58 0.054
75
BLR008 Bilirubin Metabolic Disorder 58 0.054
76
P GST044 Gastritis 58 0.054
77
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.054
78
SPN035 Spindle Cell Sarcoma 57 0.054
79
c MCR113 Microvascular Complications of Diabetes 3 55 0.054
80
P SML001 Small Cell Carcinoma 55 0.054
81
HMC014 Homocysteinemia 54 0.054
82
SPP010 Suppressor of Tumorigenicity 3 54 0.054
83
P HYP083 Hypopituitarism 53 0.054
84
P MYT002 Myotonic Dystrophy 52 0.054
85
SRS001 Serous Cystadenocarcinoma 51 0.054
86
c NNS007 Nonsyndromic Deafness 51 0.054
87
CLR109 Colorectal Adenocarcinoma 51 0.054
88
BNR002 Bone Resorption Disease 51 0.054
89
c FNC029 Fanconi Anemia, Complementation Group I 50 0.054
90
P OPN001 Open-Angle Glaucoma 50 0.054
91
SPL018 Splenomegaly 48 0.054
92
c MCR120 Microvascular Complications of Diabetes 7 48 0.054
93
c CRV002 Cervix Uteri Carcinoma in Situ 47 0.054
94
ANX004 Anoxia 44 0.054
95
c PCH010 Pachyonychia Congenita 3 43 0.054
96
CRB138 Core Binding Factor Acute Myeloid Leukemia 43 0.054
97
c MCR130 Microvascular Complications of Diabetes 6 42 0.054
98
c MCR133 Microvascular Complications of Diabetes 4 42 0.054
99
c MJR024 Major Affective Disorder 9 42 0.054
100
CRV045 Cervical Intraepithelial Neoplasia 41 0.054
101
LRG014 Large Cell Neuroendocrine Carcinoma 41 0.054
102
c MJR022 Major Affective Disorder 8 39 0.054
103
CRB004 Cerebral Artery Occlusion 38 0.054
104
OVR105 Ovarian Serous Carcinoma 37 0.054
105
c PRG020 Paragangliomas 3 36 0.054
106
BLR028 Biliary Atresia, Extrahepatic 35 0.054
107
c DFN352 Deafness, Autosomal Recessive 8 34 0.054
108
EXN003 Exencephaly 32 0.054
109
PTT001 Pituitary Hypoplasia 30 0.054
110
MYT026 Myotonia Atrophica 25 0.054
111
NRL025 Neural Tube Closure Defect 12 0.054
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