Search results for cdc42

225 hits were found for cdc42

# Family MCID Name MIFTS Score
1
TKN001 Takenouchi-Kosaki Syndrome 35 5.073
2
P BRS047 Breast Cancer 97 4.615
3
P CLR023 Colorectal Cancer 99 3.977
4
P WSK001 Wiskott-Aldrich Syndrome 72 3.875
5
P PNC035 Pancreatic Cancer 84 3.455
6
P OVR042 Ovarian Cancer 88 3.040
7
GLB015 Glioblastoma Multiforme 75 3.040
8
ESP021 Esophageal Cancer 90 3.006
9
P NRB001 Neuroblastoma 72 2.633
10
P PHC003 Pheochromocytoma 71 2.495
11
P THR014 Thrombocytopenia 67 2.476
12
P SCH015 Schizophrenia 74 2.431
13
PNC129 Pancreatic Adenocarcinoma 68 2.431
14
CNS004 Constipation 58 2.431
15
P LSS002 Lissencephaly 51 2.431
16
c AMY091 Amyotrophic Lateral Sclerosis 1 89 2.402
17
P PRK057 Parkinson Disease, Late-Onset 78 2.402
18
SHG001 Shigellosis 60 2.402
19
SML019 Smallpox 56 2.402
20
NM001 Noma 38 1.788
21
DRR016 Diarrhea 2, with Microvillus Atrophy 60 1.764
22
TMP009 Temperature-Sensitive Lethal Mutation 10 1.764
23
P RTN008 Retinitis Pigmentosa 79 1.736
24
P ADM011 Adams-Oliver Syndrome 59 1.736
25
ARS001 Aarskog-Scott Syndrome 57 1.736
26
CLS016 Clostridium Difficile Colitis 48 1.699
27
c CHR421 Charcot-Marie-Tooth Disease, Type 4h 46 1.699
28
NNS032 Non-Syndromic X-Linked Intellectual Disability 43 1.699
29
CRY030 Cryptophthalmos, Unilateral or Bilateral, Isolated 39 1.699
30
c RTS002 Ritscher-Schinzel Syndrome 2 36 1.699
32
XLN228 X-Linked Recessive Disease 26 1.699
33
c XLN230 X-Linked Monogenic Disease 18 1.699
34
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 55 0.310
35
P MYT002 Myotonic Dystrophy 49 0.148
36
PRT037 Pertussis 65 0.141
37
P FML011 Familial Adenomatous Polyposis 72 0.126
38
P LNG032 Lung Cancer 98 0.110
39
P MLN008 Melanoma 69 0.110
40
P GLM045 Glioma 63 0.110
41
GLL048 Glial Tumor 45 0.110
42
VCC001 Vaccinia 49 0.100
43
PLY150 Polykaryocytosis Inducer 31 0.100
44
P HPT023 Hepatocellular Carcinoma 100 0.089
45
P GST053 Gastric Cancer 83 0.089
46
SQM006 Squamous Cell Carcinoma 60 0.089
47
P BCL017 B-Cell Lymphoma 58 0.089
48
AGN016 Aging 56 0.089
49
ADR040 Adrenal Gland Pheochromocytoma 46 0.089
50
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.089
51
IMM167 Immune Deficiency Disease 78 0.077
52
P LYM118 Lymphoma 68 0.077
53
OST159 Osteogenic Sarcoma 66 0.077
54
P NSP012 Nasopharyngeal Carcinoma 66 0.077
55
c SML038 Small Cell Cancer of the Lung 65 0.077
56
P PLY014 Polycystic Kidney Disease 62 0.077
57
NTR046 Neutrophil Migration 50 0.077
58
BNR002 Bone Resorption Disease 48 0.077
59
GLC053 Glucocorticoid Deficiency 3 21 0.077
60
P PRS040 Prostate Cancer 97 0.063
61
c FNC027 Fanconi Anemia, Complementation Group a 81 0.063
62
INS024 Insulin-Like Growth Factor I 79 0.063
63
OST012 Osteoarthritis 78 0.063
64
CRV035 Cervical Cancer 76 0.063
65
BRN028 Brain Cancer 74 0.063
66
P RTN024 Retinoblastoma 73 0.063
67
MYL005 Myelofibrosis 70 0.063
68
WRN001 Werner Syndrome 69 0.063
69
P LKM002 Leukemia 68 0.063
70
SKN019 Skin Melanoma 68 0.063
71
P SKN015 Skin Carcinoma 66 0.063
72
P HYD006 Hydrocephalus 66 0.063
73
TNG002 Tangier Disease 65 0.063
74
ATH013 Atherosclerosis Susceptibility 65 0.063
75
CLF027 Cleft Palate, Isolated 64 0.063
76
BRC012 Brucellosis 64 0.063
77
P ADN016 Adenocarcinoma 64 0.063
78
P END044 Endometriosis 63 0.063
79
ATM095 Autoimmune Disease 62 0.063
80
HYP066 Hyperglycemia 61 0.063
81
P NPH012 Nephrotic Syndrome 60 0.063
82
CHL014 Cholera 59 0.063
83
P GLL022 Guillain-Barre Syndrome 59 0.063
84
P ANP001 Anaplastic Large Cell Lymphoma 58 0.063
85
c LSS005 Lissencephaly 1 56 0.063
86
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.063
87
P RTN016 Retinal Degeneration 53 0.063
88
c FML008 Familial Retinoblastoma 53 0.063
89
DYS015 Dysentery 52 0.063
90
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.063
91
HLX001 Helix Syndrome 47 0.063
92
c MLG068 Malignant Glioma 46 0.063
93
ORL015 Oral Squamous Cell Carcinoma 43 0.063
94
PRM329 Premature Aging 35 0.063
95
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.063
97
MYL069 Myeloma, Multiple 85 0.045
98
c LKM061 Leukemia, Acute Myeloid 84 0.045
99
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.045
100
P BLD134 Bladder Cancer 79 0.045
101
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.045
102
P LNG064 Lung Cancer Susceptibility 3 78 0.045
103
c TBR025 Tuberous Sclerosis 1 77 0.045
104
P NNN008 Noonan Syndrome 1 76 0.045
105
PHN003 Phenylketonuria 75 0.045
106
c ATR087 Atrial Standstill 1 75 0.045
107
SVR004 Severe Combined Immunodeficiency 73 0.045
108
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.045
109
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.045
110
P KDN018 Kidney Disease 72 0.045
111
c LKM063 Leukemia, Chronic Myeloid 72 0.045
112
HMN044 Human Immunodeficiency Virus Type 1 71 0.045
113
c CHR684 Chronic Kidney Disease 70 0.045
114
P TBR001 Tuberous Sclerosis 70 0.045
115
P HYP086 Hypothyroidism 69 0.045
116
P PNM007 Pneumonia 68 0.045
117
CHL065 Cholangiocarcinoma 68 0.045
118
c BSL007 Basal Cell Carcinoma 68 0.045
119
MLD001 Melioidosis 68 0.045
120
P CRB048 Cerebral Cavernous Malformations 67 0.045
121
P HLP001 Holoprosencephaly 67 0.045
122
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.045
123
P MSC005 Muscular Dystrophy 66 0.045
124
GRG001 Greig Cephalopolysyndactyly Syndrome 66 0.045
125
P MCR115 Microvascular Complications of Diabetes 5 66 0.045
126
P DRM053 Dermatitis, Atopic 66 0.045
127
MYL031 Myeloproliferative Neoplasm 66 0.045
128
TTN003 Tetanus 65 0.045
129
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.045
130
IRR002 Irritable Bowel Syndrome 65 0.045
131
P HRP006 Herpes Simplex 65 0.045
132
DGR001 Digeorge Syndrome 64 0.045
133
P PRD008 Periodontitis 64 0.045
134
c CNG006 Congenital Hypothyroidism 64 0.045
135
c PRC016 Pre-Eclampsia 63 0.045
136
P VSC007 Vascular Disease 63 0.045
137
CNT061 Conotruncal Heart Malformations 63 0.045
138
SKN016 Skin Disease 63 0.045
139
c GLC092 Glaucoma, Primary Open Angle 62 0.045
140
CLT003 Colitis 62 0.045
141
P MCH002 Machado-Joseph Disease 62 0.045
142
CHR619 Chromosome 2q35 Duplication Syndrome 62 0.045
143
TXC005 Toxic Shock Syndrome 62 0.045
144
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.045
145
FTT001 Fatty Liver Disease 61 0.045
146
DRM006 Dermatitis 61 0.045
147
P MYL006 Myeloid Leukemia 60 0.045
148
SPN186 Spinal Cord Injury 60 0.045
149
P SNS001 Sensorineural Hearing Loss 60 0.045
150
P BND020 Bone Disease 59 0.045
151
CHL123 Chlamydia 59 0.045
152
P DNG005 Dengue Virus 59 0.045
153
P NPH005 Nephronophthisis 59 0.045
154
HLC007 Helicobacter Pylori Infection 59 0.045
155
CRY005 Cryptococcosis 58 0.045
156
ISC004 Ischemia 58 0.045
157
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.045
158
EYD002 Eye Disease 58 0.045
159
CRV038 Cervical Squamous Cell Carcinoma 58 0.045
160
c DWL002 Dowling-Degos Disease 1 58 0.045
161
LYM027 Lymphopenia 58 0.045
162
P EXN002 Exanthem 57 0.045
163
c PLY172 Polycystic Kidney Disease 2 with or Without Polycystic Liver Disease 57 0.045
164
THR024 Thrombosis 57 0.045
165
c MST023 Mesothelioma, Malignant 57 0.045
166
P FCL005 Focal Segmental Glomerulosclerosis 57 0.045
167
ADN027 Adenomyosis 56 0.045
168
c FNC042 Fanconi Anemia, Complementation Group D2 56 0.045
169
P NRF002 Neurofibromatosis 56 0.045
170
EMB004 Embryonal Carcinoma 56 0.045
171
P PLY019 Polyneuropathy 56 0.045
172
P GST044 Gastritis 56 0.045
173
NRN004 Neuroendocrine Tumor 55 0.045
174
FDB001 Foodborne Botulism 55 0.045
175
P DRR001 Diarrhea 55 0.045
176
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.045
177
CRY003 Cryptosporidiosis 54 0.045
178
FNG017 Fungal Infectious Disease 53 0.045
179
OVR059 Ovary Adenocarcinoma 53 0.045
180
c MCR113 Microvascular Complications of Diabetes 3 52 0.045
181
P DDN001 Duodenal Ulcer 52 0.045
182
JCB001 Jacobsen Syndrome 52 0.045
183
CLR109 Colorectal Adenocarcinoma 51 0.045
184
INT079 Intrahepatic Cholangiocarcinoma 51 0.045
185
P OVR082 Overgrowth Syndrome 50 0.045
186
STM007 Stomatitis 50 0.045
187
c HRD202 Hereditary Lymphedema I 50 0.045
188
P TMP001 Temporal Lobe Epilepsy 50 0.045
189
SCH068 Schwartz-Jampel Syndrome, Type 1 49 0.045
190
P OPN001 Open-Angle Glaucoma 49 0.045
191
SCT005 Scott Syndrome 49 0.045
192
SPL018 Splenomegaly 48 0.045
193
CHR031 Chromoblastomycosis 47 0.045
194
c HYD019 Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius 47 0.045
195
c MCR120 Microvascular Complications of Diabetes 7 47 0.045
196
P OVR046 Ovarian Cyst 47 0.045
197
RTN023 Retinitis 46 0.045
198
TST014 Testicular Cancer 46 0.045
199
P BNG032 Benign Mesothelioma 46 0.045
200
INF006 Infant Botulism 45 0.045
201
NDL001 Nodular Malignant Melanoma 44 0.045
202
P OVR106 Ovarian Clear Cell Carcinoma 44 0.045
203
P DMY001 Demyelinating Polyneuropathy 43 0.045
204
CYT002 Cytokine Deficiency 42 0.045
205
c CRB094 Cerebral Cavernous Malformations 3 42 0.045
206
NRR001 Neuroretinitis 42 0.045
207
c MCR130 Microvascular Complications of Diabetes 6 41 0.045
208
c MCR133 Microvascular Complications of Diabetes 4 41 0.045
209
c FML015 Familial Nephrotic Syndrome 41 0.045
210
ANX004 Anoxia 40 0.045
211
P MGL010 Megalencephalic Leukoencephalopathy with Subcortical Cysts 2a 40 0.045
212
END011 Endometriosis of Ovary 39 0.045
213
ALL014 Allergic Encephalomyelitis 38 0.045
214
OVR094 Ovarian Epithelial Cancer 38 0.045
215
ATN021 Autoinflammatory Syndrome 36 0.045
216
LCH001 Leech Infestation 35 0.045
217
GLC105 Glucocorticoid Deficiency 4 with or Without Mineralocorticoid Deficiency 35 0.045
218
MYT011 Myotonia 34 0.045
219
GRM010 Germ Cells Tumors 34 0.045
220
ADN014 Adenomatoid Tumor 33 0.045
221
MLG164 Malignant Epithelial Tumor of Ovary 26 0.045
222
CNG092 Congenital Extrahepatic Portosystemic Shunt 23 0.045
223
c PSD047 Pseudo-Turner Syndrome 21 0.045
224
c BNG019 Benign Intermediate Mesothelioma 13 0.045
225
APC006 Apc-Associated Polyposis Conditions 12 0.045
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