Search results for FLCN

241 hits were found for FLCN

# Family MCID Name MIFTS Score
1
P TMR010 Tumor Predisposition Syndrome 69 115.094
2
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 114.458
3
INH023 Inherited Cancer-Predisposing Syndrome 53 114.458
4
BRT002 Birt-Hogg-Dube Syndrome 64 85.903
5
PNM010 Pneumothorax, Primary Spontaneous 58 55.998
6
RNL114 Renal Cell Carcinoma, Nonpapillary 79 39.975
7
P CLR023 Colorectal Cancer 100 35.909
8
PTC002 Potocki-Lupski Syndrome 51 29.030
9
PNM008 Pneumothorax 54 24.699
10
CHR177 Chromophobe Renal Cell Carcinoma 54 22.854
11
P KDN017 Kidney Cancer 60 18.291
12
ONC007 Oncocytoma 49 15.716
13
CLR030 Clear Cell Renal Cell Carcinoma 54 15.077
14
SMT008 Smith-Magenis Syndrome 53 12.828
15
P RNL017 Renal Oncocytoma 54 12.337
16
P TBR001 Tuberous Sclerosis 69 11.177
17
P PLC011 Pilocytic Astrocytoma 55 11.132
18
SKN013 Skin Benign Neoplasm 49 10.628
19
ANG018 Angiomyolipoma 45 10.089
20
P CWD010 Cowden Syndrome 71 9.884
21
FBR054 Fibroma 44 9.636
22
P LYN001 Lynch Syndrome 76 9.636
23
CLL002 Collecting Duct Carcinoma 53 9.636
24
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 8.907
25
RNL065 Renal Cell Carcinoma, Papillary, 1 79 7.289
26
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 58 7.266
27
KDN015 Kidney Angiomyolipoma 46 7.266
28
LMY003 Leiomyomatosis 43 7.100
29
FML028 Familial Renal Oncocytoma 19 6.957
30
FML029 Familial Renal Papillary Carcinoma 29 6.957
31
NVS015 Nevus Comedonicus 38 6.814
32
P DRM012 Dermis Tumor 23 6.814
33
ANG017 Angiolipoma 36 6.814
34
KDN016 Kidney Benign Neoplasm 30 6.814
35
PLR022 Pleural Disease 45 6.814
36
PLR003 Pilar Sheath Acanthoma 26 6.814
37
P HRD020 Hereditary Renal Cell Carcinoma 33 6.814
38
MLT003 Multilocular Clear Cell Renal Cell Carcinoma 32 6.814
39
LMY001 Leiomyoma Cutis 32 6.814
40
SKN023 Skin Tag 41 6.814
41
ERY069 Erythrokeratoderma ''en Cocardes'' 26 1.948
42
CYS044 Cystic Disease of Lung 19 1.833
43
CYS014 Cystadenocarcinoma 51 1.758
44
GST103 Gastric Cancer, Hereditary Diffuse 68 1.656
45
P HRD200 Hereditary Breast Ovarian Cancer Syndrome 68 1.495
46
SML009 Small Intestine Adenocarcinoma 57 1.491
47
THY029 Thyroid Carcinoma 54 1.473
48
c CLR087 Colorectal Cancer 12 34 1.421
49
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 60 1.421
50
c TBR025 Tuberous Sclerosis 1 84 1.407
51
P LNG032 Lung Cancer 98 1.348
52
P PRS040 Prostate Cancer 95 1.282
53
ADN011 Adenoid Cystic Carcinoma 68 1.238
54
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 59 1.222
55
DSC014 Discoid Fibromas, Familial Multiple 17 1.181
56
c DLT002 Dilated Cardiomyopathy 79 1.181
57
P RRT020 Rare Tumor 39 1.181
58
c FML053 Familial Colorectal Cancer 47 1.111
59
BLD173 Bladder Small Cell Carcinoma 44 1.101
60
CLN015 Colon Adenocarcinoma 64 1.101
61
P SML001 Small Cell Carcinoma 52 1.085
62
IRN002 Iron Metabolism Disease 56 1.057
63
PPL002 Papillary Carcinoma 46 1.057
64
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 1.026
65
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.026
66
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 1.026
67
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.026
68
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.026
69
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 1.026
70
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.026
71
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.026
72
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 1.026
73
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 1.026
74
URM002 Uremia 47 1.026
75
MNN043 Meningioma, Familial 79 1.020
76
GLM045 Glioma 62 1.020
77
LNG099 Lung Disease 62 1.012
78
LYM007 Lymphangioleiomyomatosis 68 0.992
79
P HDC001 Headache 56 0.954
80
END057 Endometrial Cancer 71 0.936
81
P GST053 Gastric Cancer 82 0.922
82
P BRS047 Breast Cancer 97 0.873
83
P PNC035 Pancreatic Cancer 86 0.873
84
P BLD134 Bladder Cancer 79 0.779
85
GST040 Gastric Adenocarcinoma 66 0.779
86
P OVR042 Ovarian Cancer 88 0.763
87
ESP021 Esophageal Cancer 84 0.734
88
c MSM022 Mismatch Repair Cancer Syndrome 1 69 0.734
89
c GLM043 Glioma Susceptibility 9 30 0.734
90
c GLM047 Glioma Susceptibility 3 32 0.734
91
c GLM025 Glioma Susceptibility 2 29 0.734
92
P GLM040 Glioma Susceptibility 1 70 0.734
93
P OLG002 Oligodendroglioma 66 0.734
94
HLX001 Helix Syndrome 47 0.706
95
END041 Endometrial Adenocarcinoma 63 0.687
96
LNG039 Lung Squamous Cell Carcinoma 57 0.687
97
P LNG064 Lung Cancer Susceptibility 3 70 0.636
98
ADN089 Adenosquamous Lung Carcinoma 49 0.636
99
PPL004 Papillary Squamous Carcinoma 39 0.636
100
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 0.636
101
BRS099 Breast Ductal Carcinoma 61 0.519
102
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.519
103
P HYP098 Hypereosinophilic Syndrome 66 0.516
104
MYL069 Myeloma, Multiple 77 0.504
105
CHR176 Chromophil Renal Cell Carcinoma 23 0.475
106
OCC016 Occupational Asthma 33 0.453
107
c TBR026 Tuberous Sclerosis 2 71 0.453
108
c PRS070 Prostate Cancer, Hereditary, 12 22 0.449
109
c PRS071 Prostate Cancer, Hereditary, 13 25 0.449
110
c PRS117 Prostate Cancer, Hereditary, 11 24 0.449
111
c PRS114 Prostate Cancer, Hereditary, 2 33 0.449
112
c PRS097 Prostate Cancer, Hereditary, 1 38 0.449
113
ESP027 Esophagus Squamous Cell Carcinoma 45 0.449
114
PRS015 Prostate Signet Ring Cell Adenocarcinoma 25 0.449
115
P BLD062 Bile Duct Cancer 68 0.449
116
SQM016 Squamous Cell Carcinoma of Gallbladder and Extrahepatic Biliary Tract 16 0.449
117
CRC045 Carcinoma of Gallbladder and Extrahepatic Biliary Tract 20 0.449
118
CLP005 Ciliopathy 41 0.429
119
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.405
120
P LTR001 Lateral Sclerosis 58 0.405
121
ANX004 Anoxia 40 0.405
122
ADN018 Adenoma 58 0.379
123
PLM173 Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and 46,xx Sex Reversal 34 0.367
124
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.367
125
MYX005 Myxoid Liposarcoma 65 0.367
126
SKN022 Skin Squamous Cell Carcinoma 54 0.367
127
P LPS002 Liposarcoma 64 0.367
128
PSD011 Pseudovascular Skin Squamous Cell Carcinoma 16 0.367
129
ORL011 Oral Cancer 60 0.367
130
MCR013 Microphthalmia 60 0.351
131
PRV003 Perivascular Epithelioid Cell Tumor 38 0.351
132
VRS002 Virus-Associated Trichodysplasia Spinulosa 30 0.351
133
c MCR115 Microvascular Complications of Diabetes 5 65 0.320
134
MRF001 Marfan Syndrome 76 0.320
135
P CYS039 Cystic Kidney Disease 52 0.320
136
ADN012 Adenocarcinoma in Situ 42 0.320
137
PPL018 Papillary Adenocarcinoma 44 0.320
138
ERD001 Erdheim-Chester Disease 53 0.320
139
HYP266 Hypoxia 56 0.320
140
INT395 Intracranial Meningioma 48 0.286
141
MRF007 Marfanoid Hypermobility Syndrome 50 0.286
142
P ART028 Aortic Aneurysm, Familial Thoracic 4 61 0.286
143
HGH043 High Grade Glioma 46 0.286
144
GLL048 Glial Tumor 52 0.286
145
INT020 Intravenous Leiomyomatosis 36 0.286
146
SCR001 Secretory Meningioma 40 0.286
147
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.286
148
P FML364 Familial Thoracic Aortic Aneurysm and Aortic Dissection 71 0.286
149
IRN008 Iron Overload in Africa 51 0.260
150
RJS001 Ruijs-Aalfs Syndrome 47 0.260
151
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.260
152
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.260
153
HPT079 Hepatoid Adenocarcinoma 39 0.260
154
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 0.260
155
c HPT073 Hepatitis C Virus 71 0.260
156
P HPT023 Hepatocellular Carcinoma 95 0.260
157
ADL096 Adult Hepatocellular Carcinoma 60 0.260
158
LNG012 Lung Occult Squamous Cell Carcinoma 20 0.260
159
LNG019 Lung Combined Type Small Cell Carcinoma 32 0.260
160
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.260
161
PDT042 Pediatric Hepatocellular Carcinoma 50 0.260
162
PTY007 Pityriasis Rotunda 26 0.260
163
P LNG021 Lung Occult Small Cell Carcinoma 20 0.260
164
FBR086 Fibrolamellar Carcinoma 59 0.260
165
HPT011 Hepatocellular Clear Cell Carcinoma 45 0.260
166
OVR062 Ovary Serous Adenocarcinoma 25 0.260
167
LNG007 Lung Mixed Small Cell and Squamous Cell Carcinoma 20 0.260
168
PRM126 Primary Peritoneal Carcinoma 61 0.260
169
c ATR087 Atrial Standstill 1 74 0.248
170
P LYM118 Lymphoma 69 0.248
171
LYM012 Lymphoplasmacytic Lymphoma 50 0.248
172
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 0.248
173
ACS001 Acoustic Neuroma 56 0.248
174
SKN016 Skin Disease 62 0.248
175
NRL005 Neurilemmoma 60 0.248
176
ACT162 Acute Sensory Ataxic Neuropathy 24 0.248
177
P MYP004 Myopathy 67 0.248
178
RRG043 Rare Genetic Skin Disease 17 0.248
179
CMB007 Combined Immunodeficiency 56 0.202
180
IMM167 Immune Deficiency Disease 77 0.202
181
VNH007 Von Hippel-Lindau Syndrome 73 0.202
182
ADR040 Adrenal Gland Pheochromocytoma 45 0.202
183
P FML011 Familial Adenomatous Polyposis 71 0.202
184
P HNT016 Huntington Disease 73 0.202
185
LMY014 Leiomyoma, Uterine 55 0.202
186
HRD029 Hereditary Leiomyomatosis and Renal Cell Cancer 56 0.202
187
P PHC003 Pheochromocytoma 70 0.202
188
LMY002 Leiomyoma 51 0.202
189
P DRR001 Diarrhea 55 0.202
190
P LMY004 Leiomyosarcoma 62 0.202
191
CYS009 Cystadenoma 43 0.202
192
P HYP061 Hypertrophic Cardiomyopathy 69 0.202
193
P THY023 Thymoma 64 0.202
194
c THY107 Thymoma, Familial 42 0.202
195
CRN238 Corneal Dystrophy, Epithelial Basement Membrane 32 0.143
196
EMP011 Emphysema, Congenital Lobar 30 0.143
197
P FNC044 Fanconi Anemia, Complementation Group C 56 0.143
198
FRN006 Frontotemporal Dementia 68 0.143
199
ART074 Aortic Dissection 53 0.143
200
P MYF003 Myofibrillar Myopathy 50 0.143
201
P OST002 Osteoporosis 77 0.143
202
P LYS001 Loeys-Dietz Syndrome 65 0.143
203
P FLL037 Follicular Lymphoma 73 0.143
204
APR001 Apraxia 51 0.143
205
LNG108 Langerhans Cell Histiocytosis 57 0.143
206
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.143
207
P CRB048 Cerebral Cavernous Malformations 63 0.143
208
ALP103 Alpha-1-Antitrypsin Deficiency 67 0.143
209
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.143
210
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.143
211
P RSP003 Respiratory Failure 74 0.143
212
c PRG021 Paragangliomas 4 38 0.143
213
IGR001 Ige Responsiveness, Atopic 59 0.143
214
P PRG013 Paraganglioma 57 0.143
215
P MYS079 Miyoshi Muscular Dystrophy 52 0.143
216
P CTS001 Cutis Laxa 64 0.143
217
HMN009 Hemangioblastoma 53 0.143
218
CNN005 Connective Tissue Disease 66 0.143
219
c MLG084 Malignant Fibrous Histiocytoma 62 0.143
220
NRN001 Neuroendocrine Carcinoma 47 0.143
221
P EHL001 Ehlers-Danlos Syndrome 57 0.143
222
CRD001 Cardiac Tamponade 44 0.143
223
HST010 Histiocytosis 49 0.143
224
BCL002 B Cell Deficiency 40 0.143
225
RLP001 Relapsing Polychondritis 55 0.143
226
P NML001 Nemaline Myopathy 49 0.143
227
c CRB191 Cerebral Cavernous Malformations 2 45 0.143
228
OST159 Osteogenic Sarcoma 66 0.143
229
GST019 Gastrointestinal Stromal Tumor 78 0.143
230
P FBR003 Fibrous Histiocytoma 43 0.143
231
P NRB001 Neuroblastoma 66 0.143
232
CVR010 Cavernous Malformation 29 0.143
233
P HYP265 Hypotonia 42 0.143
234
c CRB051 Cerebral Cavernous Malformation, Familial 41 0.143
235
HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 61 0.143
236
CHR178 Chromosomal Triplication 34 0.143
237
CHL109 Childhood Apraxia of Speech 44 0.143
238
P PPL026 Papular Mucinosis 24 0.143
239
END051 Endolymphatic Sac Tumor 23 0.143
240
LRN003 Learning Disability 49 0.143
241
P HMC002 Homocystinuria 52 0.143
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