Search results for map3k7

159 hits were found for map3k7

# Family MCID Name MIFTS Score
1
CRD221 Cardiospondylocarpofacial Syndrome 43 45.230
2
c FRN048 Frontometaphyseal Dysplasia 2 35 42.511
3
P FRN012 Frontometaphyseal Dysplasia 51 28.304
4
P HRP006 Herpes Simplex 65 16.413
5
SYN005 Synostosis 43 15.051
6
HYP068 Hyperostosis 47 12.542
7
P BRC006 Brachydactyly 52 12.467
8
ERM002 Ear Malformation 37 8.132
9
P ATL001 Atelosteogenesis 34 8.132
10
P OTP008 Otopalatodigital Syndrome Spectrum Disorder 25 8.132
11
P PRS040 Prostate Cancer 95 3.237
12
P HPT023 Hepatocellular Carcinoma 95 2.358
13
P BRS047 Breast Cancer 97 1.955
14
P PNC035 Pancreatic Cancer 87 1.737
15
c ATL011 Atelosteogenesis, Type I 36 1.716
16
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.709
17
P GST053 Gastric Cancer 82 1.705
18
KLD004 Keloid Disorder 38 1.472
19
OST015 Osteochondrodysplasia 60 1.395
20
MYL069 Myeloma, Multiple 76 1.334
21
P LNG032 Lung Cancer 98 1.331
22
P LKM002 Leukemia 65 1.321
23
PLM173 Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and 46,xx Sex Reversal 34 1.287
24
SKN022 Skin Squamous Cell Carcinoma 53 1.287
25
PSD011 Pseudovascular Skin Squamous Cell Carcinoma 16 1.287
26
P LKM062 Leukemia, Acute Lymphoblastic 69 1.265
27
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 1.265
28
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 1.265
29
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.201
30
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.178
31
STM007 Stomatitis 52 1.102
32
P MLN008 Melanoma 75 1.073
33
NRL016 Neural Tube Defects 80 1.041
34
SPN221 Spina Bifida Occulta 39 1.041
35
HRT012 Heart Valve Disease 53 1.006
36
TRS030 Tarsal Coalition 25 0.966
37
c BRN108 Branchiootic Syndrome 1 63 0.966
38
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.966
39
LPD008 Lipid Metabolism Disorder 61 0.966
40
SYN007 Synovitis 54 0.966
41
PLC002 Plica Syndrome 35 0.966
42
OST012 Osteoarthritis 77 0.966
43
FTT001 Fatty Liver Disease 61 0.966
44
HYP706 Hypermobile Ehlers-Danlos Syndrome 54 0.966
45
ADN011 Adenoid Cystic Carcinoma 68 0.940
46
PNC129 Pancreatic Adenocarcinoma 64 0.919
47
XLN240 X-Linked Otopalatodigital Spectrum Disorders 14 0.919
48
CYT002 Cytokine Deficiency 43 0.919
49
PNT038 Peanut Allergy 45 0.857
50
P AMY004 Amyloidosis 69 0.857
51
c AMY009 Amyloidosis Aa 47 0.857
52
P OVR042 Ovarian Cancer 88 0.850
53
IRN008 Iron Overload in Africa 50 0.743
54
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 0.743
55
c HPT073 Hepatitis C Virus 70 0.743
56
RJS001 Ruijs-Aalfs Syndrome 47 0.743
57
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.743
58
ADL096 Adult Hepatocellular Carcinoma 60 0.743
59
HPT079 Hepatoid Adenocarcinoma 39 0.743
60
PDT042 Pediatric Hepatocellular Carcinoma 51 0.743
61
P LNG021 Lung Occult Small Cell Carcinoma 20 0.743
62
LNG019 Lung Combined Type Small Cell Carcinoma 34 0.743
63
FBR086 Fibrolamellar Carcinoma 59 0.743
64
HPT011 Hepatocellular Clear Cell Carcinoma 46 0.743
65
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.743
66
PTY007 Pityriasis Rotunda 27 0.743
67
P TMR010 Tumor Predisposition Syndrome 69 0.665
68
END057 Endometrial Cancer 76 0.665
69
P LNG064 Lung Cancer Susceptibility 3 69 0.665
70
BLD173 Bladder Small Cell Carcinoma 44 0.665
71
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 0.665
72
CRV013 Cervical Adenoid Cystic Carcinoma 35 0.665
73
LNG039 Lung Squamous Cell Carcinoma 57 0.665
74
ADN089 Adenosquamous Lung Carcinoma 51 0.665
75
GST040 Gastric Adenocarcinoma 66 0.665
76
BRK010 Burkitt Lymphoma 65 0.517
77
RNL077 Renal Fibrosis 46 0.364
78
SPL018 Splenomegaly 47 0.364
79
P RCT021 Rectum Cancer 54 0.332
80
CLF027 Cleft Palate, Isolated 64 0.297
81
SQM006 Squamous Cell Carcinoma 59 0.297
82
P SCL018 Scoliosis 57 0.257
83
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.257
84
c SPN225 Spondyloarthropathy 1 70 0.257
85
c ATM024 Autoimmune Pancreatitis 52 0.257
86
SPN051 Spondylitis 51 0.257
87
P PNC044 Pancreatitis 61 0.257
88
TXC005 Toxic Shock Syndrome 61 0.257
89
INF009 Inflammatory Spondylopathy 30 0.257
90
NRM001 Neuromyelitis Optica 60 0.257
91
ATH013 Atherosclerosis Susceptibility 63 0.210
92
P BLD134 Bladder Cancer 79 0.210
93
HLX001 Helix Syndrome 47 0.210
94
HLC007 Helicobacter Pylori Infection 67 0.210
95
P NPH012 Nephrotic Syndrome 61 0.210
96
P PLM036 Pulmonary Fibrosis 65 0.210
97
P AGG001 Aggressive Periodontitis 55 0.210
98
P CRD246 Cardiovascular System Disease 55 0.210
99
P PRD008 Periodontitis 63 0.210
100
MSL001 Measles 61 0.210
101
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.149
102
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.149
103
P SYN057 Syndromic Intellectual Disability 38 0.149
104
c ATS204 Autosomal Recessive Non-Syndromic Intellectual Disability 47 0.149
105
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.149
106
P RHM011 Rheumatoid Arthritis 81 0.149
107
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.149
108
PPL052 Papillomatosis, Confluent and Reticulated 34 0.149
109
P RTN024 Retinoblastoma 72 0.149
110
c SML038 Small Cell Cancer of the Lung 68 0.149
111
MYP106 Myopathy, Myosin Storage, Autosomal Recessive 33 0.149
112
PLY150 Polykaryocytosis Inducer 29 0.149
113
P CLD001 Cleidocranial Dysplasia 64 0.149
114
GST092 Gastroesophageal Reflux 59 0.149
115
P CLR023 Colorectal Cancer 100 0.149
116
P MLT020 Multiple Sclerosis 79 0.149
117
c LKM061 Leukemia, Acute Myeloid 83 0.149
118
AGN016 Aging 53 0.149
119
c CFF013 Coffin-Siris Syndrome 8 25 0.149
120
EWN003 Ewing Sarcoma 69 0.149
121
CHR568 Chromosome 6q24-Q25 Deletion Syndrome 32 0.149
122
INT328 Intellectual Developmental Disorder with Dysmorphic Facies and Behavioral Abnormalities 25 0.149
123
WLF001 Wolff-Parkinson-White Syndrome 63 0.149
124
BRN133 Bronchomalacia 32 0.149
125
P KBK002 Kabuki Syndrome 1 66 0.149
126
P STR020 Strabismus 56 0.149
127
c CNG511 Congenital Heart Defects, Multiple Types, 2 24 0.149
128
c ATR087 Atrial Standstill 1 74 0.149
129
P ANG001 Angelman Syndrome 64 0.149
130
P LKM071 Leukemia, Chronic Lymphocytic 74 0.149
131
ESP021 Esophageal Cancer 84 0.149
132
P MLN069 Melanoma, Uveal 59 0.149
133
P FNC044 Fanconi Anemia, Complementation Group C 56 0.149
134
EPD015 Epidemic Typhus 44 0.149
135
DFF005 Diffuse Large B-Cell Lymphoma 55 0.149
136
MNT001 Mantle Cell Lymphoma 65 0.149
137
MRG003 Marginal Zone B-Cell Lymphoma 52 0.149
138
GLB002 Glioblastoma 67 0.149
139
c MNT227 Mental Retardation, Autosomal Recessive 46 24 0.149
140
CRB006 Cribriform Carcinoma 34 0.149
141
ISC004 Ischemia 61 0.149
142
P HYP086 Hypothyroidism 68 0.149
143
P PLY011 Polycystic Ovary Syndrome 57 0.149
144
SCR008 Scrub Typhus 57 0.149
145
SVR001 Severe Acute Respiratory Syndrome 68 0.149
146
MST005 Mastitis 52 0.149
147
P THR014 Thrombocytopenia 66 0.149
148
SCH014 Schistosomiasis 56 0.149
149
P VSC011 Vasculitis 61 0.149
150
P MYL006 Myeloid Leukemia 60 0.149
151
P NRC002 Narcolepsy 55 0.149
152
MCH006 Mechanical Strabismus 40 0.149
153
P BCL017 B-Cell Lymphoma 57 0.149
154
LNG099 Lung Disease 62 0.149
155
SYS003 Systolic Heart Failure 49 0.149
156
OVR094 Ovarian Epithelial Cancer 39 0.149
157
c CLD019 Cleidocranial Dysplasia Spectrum Disorder 20 0.149
158
P HYP265 Hypotonia 42 0.149
159
THY029 Thyroid Carcinoma 55 0.149
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