Search results for FGF10

280 hits were found for FGF10

# Family MCID Name MIFTS Score
1
LCR014 Lacrimoauriculodentodigital Syndrome 58 39.793
2
APL002 Aplasia of Lacrimal and Salivary Glands 55 38.261
3
P CRN037 Craniosynostosis 67 14.676
4
CLF001 Cleft Lip 54 13.591
5
P HYP040 Hypospadias 51 13.102
6
APR006 Apert Syndrome 69 12.852
7
CLF027 Cleft Palate, Isolated 64 12.049
8
BRN056 Bronchopulmonary Dysplasia 57 11.955
9
P PLR004 Pleuropulmonary Blastoma 65 10.593
10
DNT012 Dental Caries 53 10.555
11
TTH002 Tooth Agenesis 61 9.801
12
P ECT006 Ectodermal Dysplasia 62 9.773
13
PFF001 Pfeiffer Syndrome 77 9.742
14
MCS002 Mucositis 55 9.477
15
P CLR001 Clear Cell Acanthoma 34 9.477
16
ACN010 Acanthoma 38 9.477
17
PLM134 Pulmonary Fibrosis, Idiopathic 76 8.482
18
INT060 Intestinal Atresia 40 8.088
19
DDN011 Duodenal Atresia 47 8.064
20
CHR619 Chromosome 2q35 Duplication Syndrome 64 7.779
21
DBL002 Double Outlet Right Ventricle 56 7.779
22
DGR001 Digeorge Syndrome 62 7.737
23
P RNL100 Renal Hypodysplasia/aplasia 1 63 7.636
24
c DPH024 Diaphragmatic Hernia, Congenital 63 7.119
25
MSN003 Mesenteric Vascular Occlusion 24 7.051
26
P TTR001 Tetralogy of Fallot 69 6.997
27
MNK003 Muenke Syndrome 57 6.966
28
CRZ001 Crouzon Syndrome 64 6.888
29
HLT001 Holt-Oram Syndrome 66 6.888
30
GLL008 Gilles De La Tourette Syndrome 64 6.834
31
JCK001 Jackson-Weiss Syndrome 49 6.834
32
c ATS204 Autosomal Recessive Non-Syndromic Intellectual Disability 47 6.702
33
ULN003 Ulnar-Mammary Syndrome 56 6.702
34
ANS023 Anus, Imperforate 56 6.702
35
SRS007 Sorsby Fundus Dystrophy 51 6.702
36
c EXD012 Exudative Vitreoretinopathy 7 37 6.702
37
P ORF002 Orofacial Cleft 43 6.702
38
c DFN182 Deafness, Autosomal Recessive 71 36 6.702
39
c DVL050 Developmental and Epileptic Encephalopathy 24 37 6.702
40
PHY002 Physical Disorder 40 6.702
41
GST026 Gastric Fundus Cancer 32 6.702
42
DPH021 Diaphragm Disease 43 6.702
43
CHR088 Chronic Inflammation of Lacrimal Passage 28 6.702
44
DCR002 Dacryocystocele 36 6.702
45
FRN003 Frontal Convexity Meningioma 31 6.702
46
LNG099 Lung Disease 62 2.411
47
P MYP006 Myopia 55 2.401
48
P PLM036 Pulmonary Fibrosis 65 2.114
49
P BRS047 Breast Cancer 97 1.859
50
P PNC035 Pancreatic Cancer 87 1.767
51
ISC004 Ischemia 61 1.760
52
CLF004 Cleft Lip/palate 56 1.627
53
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.603
54
ESP020 Esophageal Atresia 59 1.509
55
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 52 1.448
56
SPN186 Spinal Cord Injury 60 1.432
57
CLN022 Colonic Atresia 25 1.375
58
BRN071 Brain Injury 50 1.361
59
P LNG032 Lung Cancer 98 1.306
60
DFN358 Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia 34 1.277
61
PST011 Pustulosis of Palm and Sole 52 1.259
62
P PSR002 Psoriasis 63 1.259
63
P RSP003 Respiratory Failure 73 1.215
64
BLD129 Bladder Exstrophy-Epispadias-Cloacal Exstrophy Complex 41 1.199
65
BLD130 Bladder Exstrophy 44 1.199
66
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 1.184
67
P MYC008 Myocarditis 59 1.184
68
HRW001 Hair Whorl 35 1.151
69
P PRS040 Prostate Cancer 95 1.134
70
DWN001 Down Syndrome 70 1.133
71
P PLM037 Pulmonary Hypertension 69 1.133
72
NLX003 Neu-Laxova Syndrome 2 47 1.133
73
CRB004 Cerebral Artery Occlusion 45 1.115
74
P VNT002 Ventricular Septal Defect 58 1.077
75
SVR004 Severe Combined Immunodeficiency 70 1.077
76
CLF056 Cleft Lip with or Without Cleft Palate 43 1.077
77
P SHR001 Short Bowel Syndrome 53 1.057
78
P INT070 Intestinal Obstruction 57 1.057
79
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.035
80
EMB002 Embryoma 37 1.035
81
P BLD134 Bladder Cancer 79 1.013
82
P PLM182 Pulmonary Hypoplasia, Primary 32 1.013
83
ESP029 Esophageal Atresia/tracheoesophageal Fistula 28 1.013
84
TRM010 Traumatic Brain Injury 50 1.013
85
c EXS020 Exostoses, Multiple, Type Ii 38 0.989
86
c MYP044 Myopia 10 18 0.989
87
KRT002 Keratomalacia 54 0.989
88
VTR016 Vater/vacterl Association 50 0.963
89
P RTN024 Retinoblastoma 72 0.963
90
TTH032 Tooth Size 35 0.963
91
CHL065 Cholangiocarcinoma 57 0.963
92
P EYD002 Eye Disease 57 0.963
93
INT079 Intrahepatic Cholangiocarcinoma 51 0.963
94
VCT001 Vacterl Association 46 0.963
95
CYT002 Cytokine Deficiency 43 0.963
96
RNL077 Renal Fibrosis 46 0.934
97
SPP011 Suppression of Tumorigenicity 12 61 0.934
98
P PLY006 Polydactyly 58 0.934
99
P BRS044 Breast Adenocarcinoma 58 0.934
100
BP1002 Bap1 Tumor Predisposition Syndrome 42 0.934
101
RFR003 Refractive Error 41 0.934
102
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.903
103
c MCR256 Microphthalmia, Syndromic 9 60 0.903
104
FTT001 Fatty Liver Disease 61 0.903
105
TRC097 Tracheomalacia 43 0.868
106
FRY006 Fryns Microphthalmia Syndrome 52 0.826
107
MCR013 Microphthalmia 59 0.826
108
GST040 Gastric Adenocarcinoma 66 0.805
109
ANL022 Anal Fistula 47 0.771
110
c CRP023 Carpenter Syndrome 1 59 0.771
111
c CHR711 Chronic Asthma 41 0.771
112
INT066 Interstitial Lung Disease 60 0.771
113
P OVR042 Ovarian Cancer 88 0.731
114
P LNG064 Lung Cancer Susceptibility 3 69 0.652
115
BLD170 Bladder Exstrophy and Epispadias Complex 43 0.639
116
HYD002 Hydronephrosis 58 0.639
117
LNG039 Lung Squamous Cell Carcinoma 57 0.548
118
P GST053 Gastric Cancer 82 0.520
119
END057 Endometrial Cancer 76 0.520
120
MYL031 Myeloproliferative Neoplasm 66 0.517
121
P LVR013 Liver Disease 68 0.476
122
SKN016 Skin Disease 63 0.476
123
P KLL001 Kallmann Syndrome 65 0.418
124
P TMR010 Tumor Predisposition Syndrome 69 0.388
125
ADN011 Adenoid Cystic Carcinoma 68 0.388
126
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.388
127
BLD173 Bladder Small Cell Carcinoma 44 0.388
128
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 0.388
129
P LNG021 Lung Occult Small Cell Carcinoma 20 0.388
130
LNG019 Lung Combined Type Small Cell Carcinoma 34 0.388
131
ADN089 Adenosquamous Lung Carcinoma 51 0.388
132
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.388
133
LNG012 Lung Occult Squamous Cell Carcinoma 20 0.388
134
LNG007 Lung Mixed Small Cell and Squamous Cell Carcinoma 20 0.388
135
AML029 Ameloblastoma 46 0.374
136
DDN009 Duodenal Obstruction 34 0.374
137
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.349
138
P SCH015 Schizophrenia 74 0.349
139
c PNC106 Pancreatic Agenesis 1 51 0.324
140
P HYP086 Hypothyroidism 68 0.324
141
PNC034 Pancreas Disease 49 0.324
142
CHR178 Chromosomal Triplication 33 0.324
143
ALL003 Allergic Rhinitis 66 0.295
144
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 68 0.295
145
P HRT032 Heart Disease 84 0.295
146
P RHN004 Rhinitis 56 0.295
147
BRN024 Bronchitis 67 0.295
148
HMM005 Hemimelia 35 0.295
149
SNG003 Single Ventricular Heart 30 0.295
150
P PRR016 Pierre Robin Syndrome 50 0.264
151
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.264
152
CHR381 Chromosome 17q23.1-Q23.2 Deletion Syndrome 34 0.264
153
HLX001 Helix Syndrome 47 0.264
154
c EXS019 Exostoses, Multiple, Type I 54 0.264
155
TRC005 Tracheal Stenosis 43 0.264
156
P OPN001 Open-Angle Glaucoma 55 0.264
157
ISL075 Isolated Pierre Robin Sequence 29 0.264
158
c VSC019 Vesicoureteral Reflux 1 56 0.229
159
c WLM013 Wilms Tumor 1 65 0.229
160
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.229
161
PLY150 Polykaryocytosis Inducer 29 0.229
162
P CLD001 Cleidocranial Dysplasia 64 0.229
163
TTH030 Teeth, Supernumerary 32 0.229
164
c BRN108 Branchiootic Syndrome 1 63 0.229
165
c HYP548 Hypogonadotropic Hypogonadism 2 with or Without Anosmia 37 0.229
166
P FBR017 Fibrosarcoma 55 0.229
167
P LPS002 Liposarcoma 64 0.229
168
P LMY004 Leiomyosarcoma 62 0.229
169
P ACN011 Acne 55 0.229
170
SYN005 Synostosis 43 0.229
171
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.229
172
c CLD019 Cleidocranial Dysplasia Spectrum Disorder 20 0.229
173
HYP266 Hypoxia 56 0.229
174
CYS001 Cystic Fibrosis 77 0.187
175
OTT002 Otitis Media 70 0.187
176
NRL016 Neural Tube Defects 80 0.187
177
c SML038 Small Cell Cancer of the Lung 68 0.187
178
TND004 Tendinopathy 45 0.187
179
TND005 Tendinitis 53 0.187
180
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.187
181
STH001 Saethre-Chotzen Syndrome 65 0.187
182
P PRK057 Parkinson Disease, Late-Onset 79 0.187
183
c CRN278 Craniosynostosis 1 55 0.187
184
CHR005 Chorioamnionitis 50 0.187
185
NNS002 Nonspecific Interstitial Pneumonia 42 0.187
186
SQM006 Squamous Cell Carcinoma 59 0.187
187
BCT022 Bacterial Infectious Disease 55 0.187
188
ADN018 Adenoma 58 0.187
189
P PNM007 Pneumonia 64 0.187
190
RNL025 Renal Hypoplasia 46 0.187
191
BLR001 Biliary Atresia 55 0.187
192
P ADN016 Adenocarcinoma 63 0.187
193
PLC005 Placental Insufficiency 55 0.187
194
P TRT010 Teratoma 50 0.187
195
END062 Endometrial Hyperplasia 47 0.187
196
CHL014 Cholera 62 0.187
197
c 46X082 46,xy Sex Reversal 52 0.187
198
c SPR009 Sporadic Breast Cancer 42 0.187
199
P INF038 Influenza 68 0.187
200
CYS021 Cystic Adenomatoid Malformation of Lung 33 0.187
201
ORF053 Orofacial Clefting Syndrome 31 0.187
202
P OVR082 Overgrowth Syndrome 41 0.187
203
c ATS007 Autism Spectrum Disorder 71 0.132
204
P SCL018 Scoliosis 57 0.132
205
ORL015 Oral Squamous Cell Carcinoma 43 0.132
206
P PRT042 Parietal Foramina 51 0.132
207
VLC001 Velocardiofacial Syndrome 57 0.132
208
P ATS364 Autism 72 0.132
209
CNT061 Conotruncal Heart Malformations 66 0.132
210
c FRS014 Fraser Syndrome 1 56 0.132
211
c TYP009 Type 2 Diabetes Mellitus 91 0.132
212
LRW001 Leri-Weill Dyschondrosteosis 43 0.132
213
P THN009 Thanatophoric Dysplasia, Type I 62 0.132
214
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.132
215
DST033 Distichiasis 35 0.132
216
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.132
217
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.132
218
RDL037 Radial Ray Deficiency, X-Linked 15 0.132
219
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.132
220
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.132
221
P FML011 Familial Adenomatous Polyposis 70 0.132
222
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.132
223
MMM006 Mammographic Density 39 0.132
224
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.132
225
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 50 0.132
226
THR009 Thrombocytopenia-Absent Radius Syndrome 53 0.132
227
CHR103 Charge Syndrome 65 0.132
228
P SJG008 Sjogren Syndrome 60 0.132
229
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.132
230
c ART101 Aortic Valve Disease 2 65 0.132
231
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.132
232
c PCH010 Pachyonychia Congenita 3 43 0.132
233
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.132
234
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.132
235
P VND007 Van Der Woude Syndrome 1 60 0.132
236
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.132
237
LYM029 Lymphedema-Distichiasis Syndrome 52 0.132
238
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.132
239
PRS129 Prostatic Hyperplasia, Benign 48 0.132
240
P BND020 Bone Disease 60 0.132
241
c HRD202 Hereditary Lymphedema I 54 0.132
242
HYP060 Hyperinsulinism 53 0.132
243
HYP080 Hypogonadism 49 0.132
244
P TCD001 Tic Disorder 50 0.132
245
P BNG032 Benign Mesothelioma 53 0.132
246
CLC006 Calcinosis 47 0.132
247
DYS018 Dysostosis 43 0.132
248
P BRS053 Breast Fibroadenoma 48 0.132
249
P HYP730 Hypogonadotropic Hypogonadism 57 0.132
250
P TRN020 Turner Syndrome 67 0.132
251
P GLL018 Gallbladder Cancer 59 0.132
252
XRP001 Xerophthalmia 42 0.132
253
SPN035 Spindle Cell Sarcoma 51 0.132
254
PRS021 Prostatic Adenoma 43 0.132
255
PPL001 Papillary Adenoma 44 0.132
256
RCK004 Rickets 64 0.132
257
PRS045 Prostatic Hypertrophy 53 0.132
258
P ART005 Arteriovenous Malformation 64 0.132
259
P HRD008 Hereditary Hemorrhagic Telangiectasia 64 0.132
260
P AXN002 Axenfeld-Rieger Syndrome 62 0.132
261
P GND004 Gonadal Dysgenesis 46 0.132
262
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.132
263
SRC014 Sarcoma 64 0.132
264
NNT004 Neonatal Respiratory Failure 36 0.132
265
LYM009 Lymphocytic Choriomeningitis 46 0.132
266
TLN003 Telangiectasis 51 0.132
267
KRT001 Keratoconjunctivitis Sicca 49 0.132
268
P INF032 Infertility 60 0.132
269
PTT001 Pituitary Hypoplasia 34 0.132
270
STS002 Situs Inversus 44 0.132
271
FBR019 Fibromatosis 44 0.132
272
P HRP006 Herpes Simplex 65 0.132
273
SYN106 Syndromic Craniosynostosis 35 0.132
274
SFT003 Soft Tissue Sarcoma 43 0.132
275
MCR103 Microtia 40 0.132
276
P RRT020 Rare Tumor 39 0.132
277
EXN003 Exencephaly 30 0.132
278
FTL029 Fetal Thalidomide Syndrome 27 0.132
279
P HYP265 Hypotonia 42 0.132
280
P RNL123 Renal Agenesis, Bilateral 37 0.132
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