Search results for "[genes] RET"

89 hits were found for '[genes] RET'

# Family MCID Name MIFTS Score
1
P HRS035 Hirschsprung Disease 1 58 23.875
2
THY028 Thyroid Cancer 69 20.178
3
c MLT024 Multiple Endocrine Neoplasia Iia 64 20.178
4
P MDL022 Medullary Thyroid Carcinoma, Familial 63 20.178
5
P PHC003 Pheochromocytoma 71 19.143
6
P RNL100 Renal Hypodysplasia/aplasia 1 53 18.048
7
CNT097 Central Hypoventilation Syndrome, Congenital 59 16.882
8
P MLT074 Multiple Endocrine Neoplasia 56 16.882
9
c MLT025 Multiple Endocrine Neoplasia Iib 56 16.882
10
P NRF002 Neurofibromatosis 71 15.630
11
P PRG013 Paraganglioma 54 15.630
12
P CLR023 Colorectal Cancer 97 14.268
13
VNH007 Von Hippel-Lindau Syndrome 69 14.268
14
HSH003 Hashimoto Thyroiditis 62 14.268
15
P HYP069 Hyperparathyroidism 58 14.268
16
NRN004 Neuroendocrine Tumor 56 14.268
17
P WRD001 Waardenburg's Syndrome 55 14.268
18
THY103 Thyroid Cancer, Monmedullary, 1 53 14.268
19
PPL002 Papillary Carcinoma 51 14.268
20
END035 Endocrine Gland Cancer 49 14.268
21
PRT029 Parathyroid Adenoma 48 14.268
22
FLL031 Follicular Adenoma 42 14.268
23
c MLT136 Multiple Endocrine Neoplasia 1 69 12.762
24
P THY102 Thyroid Cancer, Nonmedullary, 2 58 12.762
25
CNS004 Constipation 57 12.762
26
c HYP615 Hyperparathyroidism, Familial Primary 56 12.762
27
P THY032 Thyroiditis 54 12.762
28
ACH005 Achalasia 52 12.762
29
NRM004 Neuroma 48 12.762
30
PRT030 Parathyroid Gland Disease 47 12.762
31
c INT072 Intestinal Pseudo-Obstruction 46 12.762
32
NDL007 Nodular Goiter 46 12.762
33
PYL006 Pyloric Stenosis 46 12.762
34
MGC001 Megacolon 45 12.762
35
P HYP009 Hypertrophic Pyloric Stenosis 42 12.762
36
PHC013 Phaeochromocytoma 41 12.762
37
P HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 40 12.762
38
P STR021 Struma Ovarii 39 12.762
39
c SPR094 Sporadic Pheochromocytoma 36 12.762
40
P CWD001 Cowden Disease 64 11.052
41
ADM013 Adamantinoma of Long Bones 57 11.052
42
P INT070 Intestinal Obstruction 57 11.052
43
c PRM126 Primary Peritoneal Carcinoma 54 11.052
44
SHP002 Shprintzen-Goldberg Syndrome 53 11.052
45
CLN019 Colonic Disease 51 11.052
46
HYP108 Hyperparathyroidism-Jaw Tumor Syndrome 47 11.052
47
PRT009 Parotid Gland Cancer 44 11.052
48
PLM039 Pulmonary Neuroendocrine Tumor 42 11.052
49
SHL001 Shoulder Impingement Syndrome 42 11.052
50
THY049 Thyroid Cancer, Anaplastic 42 11.052
51
c WRD020 Waardenburg Syndrome, Type 4a 42 11.052
52
MDL009 Medullary Sponge Kidney 41 11.052
53
ADN010 Adenosquamous Cell Lung Carcinoma 41 11.052
54
ATN011 Autoinflammation with Infantile Enterocolitis 39 11.052
55
LRN001 Laurence-Moon Syndrome 38 11.052
56
APP009 Appendix Adenocarcinoma 38 11.052
57
DRF001 Dirofilariasis 37 11.052
58
c MLG059 Malignant Struma Ovarii 36 11.052
59
ADR014 Adrenal Medulla Cancer 36 11.052
60
EXT054 Extra-Adrenal Pheochromocytoma 35 11.052
61
ATS009 Autosomal Genetic Disease 35 11.052
62
BRS032 Breast Papillary Carcinoma 34 11.052
63
LCH003 Lichen Nitidus 34 11.052
64
FML029 Familial Renal Papillary Carcinoma 34 11.052
65
PSD008 Pseudopapilledema 34 11.052
66
P RNL059 Renal-Hepatic-Pancreatic Dysplasia 34 11.052
67
TST043 Testicular Seminoma 30 11.052
68
LCH014 Lichen Amyloidosis 29 11.052
69
HYP572 Hypoganglionosis 29 11.052
70
FML143 Familial Papillary Thyroid Carcinoma 28 11.052
71
OVR109 Ovarian Germ Cell Teratoma 28 11.052
72
c BNG029 Benign Struma Ovarii 26 11.052
73
THY104 Thyroid Carcinoma Somatic 24 11.052
74
RNL105 Renal Agenesis, Unilateral 21 11.052
75
MLT011 Multiple Mucosal Neuroma 18 11.052
76
c RTR014 Ret-Related Hirschsprung Disease 6 11.052
77
c RTR015 Ret-Related Pheochromocytoma 5 11.052
78
P INT068 Intestinal Disease 60 9.024
79
PRG097 Paragangliomas 1, with or Without Deafness 54 9.024
80
DFF036 Differentiated Thyroid Carcinoma 50 9.024
81
ECT093 Ectopic Cushing Syndrome 43 9.024
82
c CTR103 Cataract 4, Multiple Types 39 9.024
83
c CLL012 Cell Type Benign Neoplasm 39 9.024
84
ADR040 Adrenal Gland Pheochromocytoma 33 9.024
85
c HRS036 Hirschsprung Disease 2 32 9.024
86
PRS123 Persistent Generalized Lymphadenopathy 31 9.024
87
c DFN171 Deafness, Autosomal Recessive 33 27 9.024
88
c USH030 Usher Syndrome, Type Ik 24 9.024
89
CTR009 Cataract Congenital Dominant Non Nuclear 20 9.024