Search results for "[genes] RET"

85 hits were found for '[genes] RET'

# Family MCID Name MIFTS Score
1
P HRS035 Hirschsprung Disease 1 59 24.130
2
THY028 Thyroid Cancer 70 20.394
3
c MLT024 Multiple Endocrine Neoplasia Iia 64 19.347
4
P MDL022 Medullary Thyroid Carcinoma, Familial 60 19.347
5
P PHC003 Pheochromocytoma 71 18.241
6
c MLT025 Multiple Endocrine Neoplasia Iib 54 17.063
7
CNT097 Central Hypoventilation Syndrome, Congenital 56 15.797
8
P RNL100 Renal Hypodysplasia/aplasia 1 50 15.797
9
P CLR023 Colorectal Cancer 97 14.421
10
P NRF002 Neurofibromatosis 74 14.421
11
ADN018 Adenoma 62 14.421
12
P HYP069 Hyperparathyroidism 57 14.421
13
P MLT074 Multiple Endocrine Neoplasia 55 14.421
14
PHC013 Phaeochromocytoma 49 14.421
15
P ADN016 Adenocarcinoma 69 12.898
16
VNH007 Von Hippel-Lindau Syndrome 69 12.898
17
c PRM005 Primary Hyperparathyroidism 57 12.898
18
CNS004 Constipation 57 12.898
19
P PRG013 Paraganglioma 54 12.898
20
THY103 Thyroid Cancer, Monmedullary, 1 54 12.898
21
END035 Endocrine Gland Cancer 54 12.898
22
P WRD001 Waardenburg's Syndrome 53 12.898
23
PPL002 Papillary Carcinoma 52 12.898
24
c MLT136 Multiple Endocrine Neoplasia 1 68 11.170
25
P CWD001 Cowden Disease 66 11.170
26
ACH005 Achalasia 60 11.170
27
P THY102 Thyroid Cancer, Nonmedullary, 2 58 11.170
28
PLM010 Pulmonary Edema 56 11.170
29
HSH003 Hashimoto Thyroiditis 56 11.170
30
P THY032 Thyroiditis 54 11.170
31
P INT070 Intestinal Obstruction 53 11.170
32
NRM004 Neuroma 52 11.170
33
PRT030 Parathyroid Gland Disease 50 11.170
34
P PRT029 Parathyroid Adenoma 48 11.170
35
FLL031 Follicular Adenoma 46 11.170
36
c INT072 Intestinal Pseudo-Obstruction 45 11.170
37
NDL007 Nodular Goiter 45 11.170
38
PYL006 Pyloric Stenosis 45 11.170
39
GNG002 Ganglioneuroma 44 11.170
40
P HYP009 Hypertrophic Pyloric Stenosis 42 11.170
41
P HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 39 11.170
42
c PRM126 Primary Peritoneal Carcinoma 58 9.120
43
SHP002 Shprintzen-Goldberg Syndrome 54 9.120
44
CLN019 Colonic Disease 54 9.120
45
MGC001 Megacolon 53 9.120
46
PRG097 Paragangliomas 1, with or Without Deafness 49 9.120
47
HYP108 Hyperparathyroidism-Jaw Tumor Syndrome 46 9.120
48
ADN010 Adenosquamous Cell Lung Carcinoma 46 9.120
49
PRT009 Parotid Gland Cancer 45 9.120
50
SHL001 Shoulder Impingement Syndrome 45 9.120
51
P PTT002 Potter's Syndrome 44 9.120
52
APP009 Appendix Adenocarcinoma 42 9.120
53
ATS009 Autosomal Genetic Disease 41 9.120
54
c WRD020 Waardenburg Syndrome, Type 4a 41 9.120
55
THY049 Thyroid Cancer, Anaplastic 41 9.120
56
FML029 Familial Renal Papillary Carcinoma 41 9.120
57
P RNL059 Renal-Hepatic-Pancreatic Dysplasia 41 9.120
58
PSD008 Pseudopapilledema 39 9.120
59
TXC001 Toxic Megacolon 39 9.120
60
ADR014 Adrenal Medulla Cancer 38 9.120
61
c SPR094 Sporadic Pheochromocytoma 38 9.120
62
PRS123 Persistent Generalized Lymphadenopathy 38 9.120
63
LRN001 Laurence-Moon Syndrome 37 9.120
64
LCH003 Lichen Nitidus 37 9.120
65
BRS032 Breast Papillary Carcinoma 37 9.120
66
P STR021 Struma Ovarii 36 9.120
67
c BNG029 Benign Struma Ovarii 34 9.120
68
EXT054 Extra-Adrenal Pheochromocytoma 34 9.120
69
OVR109 Ovarian Germ Cell Teratoma 31 9.120
70
NRN029 Neuronal Intestinal Dysplasia 30 9.120
71
LCH014 Lichen Amyloidosis 30 9.120
72
c MLG059 Malignant Struma Ovarii 29 9.120
73
THY104 Thyroid Carcinoma Somatic 26 9.120
74
MLT011 Multiple Mucosal Neuroma 20 9.120
75
P INT068 Intestinal Disease 64 6.449
76
DFF036 Differentiated Thyroid Carcinoma 54 6.449
77
P ORG009 Organ System Cancer 48 6.449
78
c CLL012 Cell Type Benign Neoplasm 45 6.449
79
ATS008 Autosomal Dominant Disease 43 6.449
80
c CTR103 Cataract 4, Multiple Types 43 6.449
81
ADR040 Adrenal Gland Pheochromocytoma 33 6.449
82
CTR009 Cataract Congenital Dominant Non Nuclear 27 6.449
83
RNL105 Renal Agenesis, Unilateral 20 6.449
84
c RTR014 Ret-Related Hirschsprung Disease 7 6.449
85
c RTR015 Ret-Related Pheochromocytoma 6 6.449