Search results for "[genes] RET"

86 hits were found for '[genes] RET'

# Family MCID Name MIFTS Score
1
P HRS035 Hirschsprung Disease 1 59 23.943
2
THY028 Thyroid Cancer 68 20.236
3
P MDL022 Medullary Thyroid Carcinoma, Familial 63 20.236
4
c MLT024 Multiple Endocrine Neoplasia Iia 65 19.197
5
P PHC003 Pheochromocytoma 71 18.100
6
P RNL100 Renal Hypodysplasia/aplasia 1 54 16.931
7
CNT097 Central Hypoventilation Syndrome, Congenital 60 15.675
8
c MLT025 Multiple Endocrine Neoplasia Iib 56 15.675
9
P CLR023 Colorectal Cancer 97 14.309
10
ADN018 Adenoma 59 14.309
11
P HYP069 Hyperparathyroidism 57 14.309
12
P MLT074 Multiple Endocrine Neoplasia 55 14.309
13
P NRF019 Neurofibromatosis, Type 2 73 12.798
14
P ADN016 Adenocarcinoma 69 12.798
15
VNH007 Von Hippel-Lindau Syndrome 69 12.798
16
HSH003 Hashimoto Thyroiditis 61 12.798
17
PRG097 Paragangliomas 1, with or Without Deafness 58 12.798
18
CNS004 Constipation 57 12.798
19
THY103 Thyroid Cancer, Monmedullary, 1 54 12.798
20
END035 Endocrine Gland Cancer 52 12.798
21
P WRD020 Waardenburg Syndrome, Type 4a 50 12.798
22
PPL002 Papillary Carcinoma 49 12.798
23
PRT029 Parathyroid Adenoma 47 12.798
24
FLL031 Follicular Adenoma 41 12.798
25
PHC013 Phaeochromocytoma 41 12.798
26
c MLT136 Multiple Endocrine Neoplasia 1 68 11.084
27
P CWD006 Cowden Syndrome 1 68 11.084
28
P PRT010 Parathyroid Carcinoma 62 11.084
29
P THY102 Thyroid Cancer, Nonmedullary, 2 60 11.084
30
P INT070 Intestinal Obstruction 56 11.084
31
c HYP615 Hyperparathyroidism, Familial Primary 55 11.084
32
P THY032 Thyroiditis 54 11.084
33
ACH005 Achalasia 54 11.084
34
MGC001 Megacolon 50 11.084
35
PRT030 Parathyroid Gland Disease 49 11.084
36
NRM004 Neuroma 48 11.084
37
GNG002 Ganglioneuroma 48 11.084
38
c INT072 Intestinal Pseudo-Obstruction 46 11.084
39
NDL007 Nodular Goiter 46 11.084
40
PYL006 Pyloric Stenosis 46 11.084
41
P HYP009 Hypertrophic Pyloric Stenosis 41 11.084
42
P HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 39 11.084
43
P STR021 Struma Ovarii 37 11.084
44
c SPR094 Sporadic Pheochromocytoma 35 11.084
45
ADM013 Adamantinoma of Long Bones 59 9.050
46
SHP002 Shprintzen-Goldberg Syndrome 54 9.050
47
c PRM126 Primary Peritoneal Carcinoma 54 9.050
48
CLN019 Colonic Disease 50 9.050
49
HYP108 Hyperparathyroidism-Jaw Tumor Syndrome 44 9.050
50
PRT009 Parotid Gland Cancer 43 9.050
51
ADN010 Adenosquamous Cell Lung Carcinoma 42 9.050
52
PLM039 Pulmonary Neuroendocrine Tumor 42 9.050
53
SHL001 Shoulder Impingement Syndrome 42 9.050
54
THY049 Thyroid Cancer, Anaplastic 41 9.050
55
ATN011 Autoinflammation with Infantile Enterocolitis 41 9.050
56
TST043 Testicular Seminoma 40 9.050
57
MDL009 Medullary Sponge Kidney 40 9.050
58
APP009 Appendix Adenocarcinoma 40 9.050
59
ATS009 Autosomal Genetic Disease 39 9.050
60
ADR014 Adrenal Medulla Cancer 38 9.050
61
PSD008 Pseudopapilledema 38 9.050
62
LRN001 Laurence-Moon Syndrome 38 9.050
63
DRF001 Dirofilariasis 37 9.050
64
EXT054 Extra-Adrenal Pheochromocytoma 36 9.050
65
BRS032 Breast Papillary Carcinoma 35 9.050
66
P RNL059 Renal-Hepatic-Pancreatic Dysplasia 35 9.050
67
c MLG059 Malignant Struma Ovarii 35 9.050
68
LCH003 Lichen Nitidus 35 9.050
69
FML029 Familial Renal Papillary Carcinoma 34 9.050
70
OVR109 Ovarian Germ Cell Teratoma 29 9.050
71
FML143 Familial Papillary Thyroid Carcinoma 28 9.050
72
HYP572 Hypoganglionosis 27 9.050
73
LCH014 Lichen Amyloidosis 26 9.050
74
c BNG029 Benign Struma Ovarii 25 9.050
75
THY104 Thyroid Carcinoma Somatic 23 9.050
76
MLT011 Multiple Mucosal Neuroma 18 9.050
77
P INT068 Intestinal Disease 61 6.399
78
DFF036 Differentiated Thyroid Carcinoma 47 6.399
79
c CLL012 Cell Type Benign Neoplasm 41 6.399
80
c CTR103 Cataract 4, Multiple Types 41 6.399
81
ADR040 Adrenal Gland Pheochromocytoma 34 6.399
82
c HRS036 Hirschsprung Disease 2 32 6.399
83
CTR009 Cataract Congenital Dominant Non Nuclear 23 6.399
84
RNL105 Renal Agenesis, Unilateral 23 6.399
85
c RTR014 Ret-Related Hirschsprung Disease 6 6.399
86
c RTR015 Ret-Related Pheochromocytoma 5 6.399