Search results for fgf4

197 hits were found for fgf4

# Family MCID Name MIFTS Score
1
P BRS047 Breast Cancer 97 22.957
2
P GST053 Gastric Cancer 82 17.604
3
ESP021 Esophageal Cancer 84 17.156
4
EMB004 Embryonal Carcinoma 55 16.776
5
P CRN037 Craniosynostosis 67 14.504
6
GRM005 Germ Cell Cancer 46 14.075
7
TRT001 Teratocarcinoma 41 13.749
8
SRC014 Sarcoma 64 13.664
9
CLF027 Cleft Palate, Isolated 64 10.584
10
PRP027 Peripheral Vascular Disease 71 10.584
11
APR006 Apert Syndrome 69 10.539
12
P RTT002 Rett Syndrome 79 10.479
13
P INN002 Inner Ear Disease 50 10.336
14
TST014 Testicular Cancer 51 10.336
15
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 10.336
16
CHR619 Chromosome 2q35 Duplication Syndrome 64 8.490
17
CRZ001 Crouzon Syndrome 64 8.242
18
ULN003 Ulnar-Mammary Syndrome 56 7.511
19
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 54 7.308
20
LCR014 Lacrimoauriculodentodigital Syndrome 58 7.308
21
ODN023 Odontochondrodysplasia 70 7.308
22
GLL015 Gallbladder Squamous Cell Carcinoma 31 7.308
23
GRM001 Germ Cell and Embryonal Cancer 25 7.308
24
LVR006 Liver Lymphoma 25 7.308
25
INT146 Intervertebral Disc Disease 61 2.129
26
P OVR042 Ovarian Cancer 88 1.963
27
P LNG064 Lung Cancer Susceptibility 3 70 1.737
28
P TRT010 Teratoma 50 1.704
29
GST019 Gastrointestinal Stromal Tumor 78 1.560
30
KPS004 Kaposi Sarcoma 76 1.524
31
P PLY006 Polydactyly 58 1.509
32
SMN007 Seminoma 42 1.506
33
P BLD134 Bladder Cancer 79 1.429
34
CHR074 Choriocarcinoma 46 1.375
35
SQM006 Squamous Cell Carcinoma 59 1.342
36
P LNG032 Lung Cancer 98 1.314
37
DWR001 Dwarfism 45 1.139
38
P PRS040 Prostate Cancer 95 1.119
39
LMB062 Limb Ischemia 55 1.115
40
P ADN016 Adenocarcinoma 63 1.115
41
ISC004 Ischemia 61 1.091
42
SPN186 Spinal Cord Injury 61 1.091
43
TST018 Testicular Yolk Sac Tumor 39 1.065
44
P END039 Endodermal Sinus Tumor 42 1.065
45
END057 Endometrial Cancer 71 1.040
46
P INS002 in Situ Carcinoma 53 1.036
47
P HMN032 Human Herpesvirus 8 47 1.006
48
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.006
49
LVR012 Liver Cirrhosis 62 1.006
50
DPH001 Diphtheria 59 1.006
51
SPN035 Spindle Cell Sarcoma 51 1.006
52
P CLR023 Colorectal Cancer 100 0.972
53
DSS032 Disease by Infectious Agent 55 0.933
54
SYN007 Synovitis 54 0.933
55
PLC002 Plica Syndrome 35 0.933
56
P CHR345 Chronic Pain 50 0.933
57
P HRP006 Herpes Simplex 65 0.933
58
OST012 Osteoarthritis 77 0.933
59
ORL015 Oral Squamous Cell Carcinoma 43 0.902
60
LNG039 Lung Squamous Cell Carcinoma 57 0.895
61
P SYN012 Synpolydactyly 38 0.888
62
ODN020 Odontoma-Dysphagia Syndrome 19 0.888
63
TTH002 Tooth Agenesis 61 0.888
64
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.888
65
P MCR010 Microcephaly 59 0.888
66
ODN006 Odontoma 29 0.888
67
DYS073 Dysphagia 53 0.888
68
P PNC035 Pancreatic Cancer 86 0.870
69
ART140 Arteries, Anomalies of 52 0.828
70
LPP008 Lipoprotein Quantitative Trait Locus 65 0.828
71
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.828
72
BLD173 Bladder Small Cell Carcinoma 44 0.792
73
GST040 Gastric Adenocarcinoma 66 0.790
74
c CLR087 Colorectal Cancer 12 34 0.723
75
GST103 Gastric Cancer, Hereditary Diffuse 68 0.723
76
SML009 Small Intestine Adenocarcinoma 57 0.723
77
CLN015 Colon Adenocarcinoma 64 0.723
78
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 60 0.723
79
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.685
80
SYN005 Synostosis 43 0.685
81
P TMR010 Tumor Predisposition Syndrome 69 0.647
82
ADN011 Adenoid Cystic Carcinoma 68 0.647
83
ADN089 Adenosquamous Lung Carcinoma 49 0.647
84
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 0.647
85
P HPT023 Hepatocellular Carcinoma 95 0.517
86
GLB002 Glioblastoma 67 0.472
87
TRN018 Transitional Cell Carcinoma 56 0.472
88
END041 Endometrial Adenocarcinoma 63 0.457
89
BRS099 Breast Ductal Carcinoma 61 0.457
90
c CTR174 Cataract 40 32 0.406
91
ANG054 Angina Pectoris 65 0.406
92
HRW001 Hair Whorl 35 0.406
93
P STR020 Strabismus 56 0.406
94
P CTR002 Cataract 59 0.406
95
MCH006 Mechanical Strabismus 40 0.406
96
P HMN010 Hemangioma 61 0.380
97
P BCL017 B-Cell Lymphoma 57 0.380
98
HMM005 Hemimelia 33 0.380
99
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.323
100
BRT002 Birt-Hogg-Dube Syndrome 64 0.323
101
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.323
102
RNL119 Renal Cell Carcinoma, Xp11-Associated 42 0.323
103
DST001 Distal Biliary Tract Carcinoma 24 0.323
104
LNG019 Lung Combined Type Small Cell Carcinoma 32 0.323
105
P MLN008 Melanoma 75 0.323
106
P BLD062 Bile Duct Cancer 68 0.323
107
P LNG021 Lung Occult Small Cell Carcinoma 20 0.323
108
PNS010 Penis Squamous Cell Carcinoma 45 0.323
109
CHR177 Chromophobe Renal Cell Carcinoma 54 0.323
110
OVR062 Ovary Serous Adenocarcinoma 25 0.323
111
PNS005 Penis Mixed Squamous Cell Carcinoma 12 0.323
112
PRM126 Primary Peritoneal Carcinoma 61 0.323
113
c PRC016 Pre-Eclampsia 64 0.321
114
P NRB001 Neuroblastoma 66 0.321
115
c SPL067 Split-Hand/foot Malformation 1 46 0.287
116
ISL121 Isolated Split Hand-Split Foot Malformation 42 0.287
117
P OVR082 Overgrowth Syndrome 42 0.287
118
c EXS019 Exostoses, Multiple, Type I 54 0.248
119
c EXS020 Exostoses, Multiple, Type Ii 38 0.248
120
P VSC007 Vascular Disease 62 0.248
121
P RHB003 Rhabdomyosarcoma 66 0.248
122
DGN001 Degenerative Disc Disease 48 0.248
123
ORL011 Oral Cancer 60 0.248
124
RNP003 Renpenning Syndrome 1 48 0.203
125
P DRR005 Diarrhea 4, Malabsorptive, Congenital 37 0.203
126
PLY150 Polykaryocytosis Inducer 29 0.203
127
P ATR011 Atrial Fibrillation 66 0.203
128
DFN358 Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia 33 0.203
129
DYS018 Dysostosis 43 0.203
130
P OLG002 Oligodendroglioma 66 0.203
131
P FBR017 Fibrosarcoma 55 0.203
132
HYP266 Hypoxia 56 0.203
133
CLF001 Cleft Lip 54 0.203
134
ANP009 Anaplastic Oligodendroglioma 41 0.203
135
c TYP009 Type 2 Diabetes Mellitus 92 0.143
136
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.143
138
CRV035 Cervical Cancer 72 0.143
139
c MCR115 Microvascular Complications of Diabetes 5 65 0.143
140
c DFN250 Deafness, Autosomal Recessive 2 45 0.143
141
c DFN112 Deafness, Autosomal Recessive 63 39 0.143
142
c NLD006 Nail Disorder, Nonsyndromic Congenital, 9 35 0.143
143
HLX001 Helix Syndrome 47 0.143
144
P KRT007 Keratoconus 50 0.143
145
OST011 Osteomalacia 52 0.143
146
RCK004 Rickets 65 0.143
147
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.143
148
NNL006 Non-Alcoholic Steatohepatitis 54 0.143
149
P PLY147 Polydactyly, Postaxial, Type A1 50 0.143
150
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.143
151
P STS008 Sotos Syndrome 1 62 0.143
152
c FNC027 Fanconi Anemia, Complementation Group a 81 0.143
153
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 53 0.143
154
P LYM118 Lymphoma 69 0.143
155
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.143
156
P FML011 Familial Adenomatous Polyposis 71 0.143
157
HYP017 Hypophosphatemia 49 0.143
158
BSL009 Basal Ganglia Calcification 45 0.143
159
ECT042 Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/palate Syndrome 3 43 0.143
160
HYP042 Hypochondroplasia 58 0.143
161
c HYP548 Hypogonadotropic Hypogonadism 2 with or Without Anosmia 37 0.143
162
P HNT016 Huntington Disease 73 0.143
163
LMY014 Leiomyoma, Uterine 55 0.143
164
PFF001 Pfeiffer Syndrome 77 0.143
165
P NNN008 Noonan Syndrome 1 76 0.143
166
c SCL052 Scleroderma, Familial Progressive 60 0.143
167
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.143
168
P RSP003 Respiratory Failure 74 0.143
169
LMY002 Leiomyoma 51 0.143
170
P INF032 Infertility 60 0.143
171
P LTR001 Lateral Sclerosis 58 0.143
172
P LMY004 Leiomyosarcoma 62 0.143
173
P BNG013 Benign Breast Phyllodes Tumor 35 0.143
174
KHN001 Kuhnt-Junius Degeneration 48 0.143
175
P PLY011 Polycystic Ovary Syndrome 57 0.143
176
PLC005 Placental Insufficiency 56 0.143
177
INT066 Interstitial Lung Disease 60 0.143
178
P ECT006 Ectodermal Dysplasia 62 0.143
179
c SCH085 Schizophrenia 2 27 0.143
180
LMB008 Limb-Mammary Syndrome 33 0.143
181
PHN003 Phenylketonuria 76 0.143
182
P NSP012 Nasopharyngeal Carcinoma 60 0.143
183
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.143
184
P GST044 Gastritis 55 0.143
186
LNG099 Lung Disease 62 0.143
187
P MYP004 Myopathy 67 0.143
188
PPT005 Peptic Ulcer Disease 58 0.143
190
HTR003 Heterotaxy 44 0.143
191
DFF035 Diffuse Cutaneous Systemic Sclerosis 45 0.143
192
ONC003 Oncogenic Osteomalacia 42 0.143
193
P ATR005 Atrophic Gastritis 50 0.143
194
c PSD047 Pseudo-Turner Syndrome 52 0.143
195
CLF056 Cleft Lip with or Without Cleft Palate 43 0.143
196
CLF004 Cleft Lip/palate 57 0.143
197
RRG078 Rare Genetic Deafness 38 0.143
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