Search results for "[genes] RET"

85 hits were found for '[genes] RET'

# Family MCID Name MIFTS Score
1
P HRS035 Hirschsprung Disease 1 55 24.130
2
THY028 Thyroid Cancer 65 20.394
3
c MLT024 Multiple Endocrine Neoplasia Iia 56 19.347
4
P MDL022 Medullary Thyroid Carcinoma, Familial 54 19.347
5
P PHC003 Pheochromocytoma 70 18.241
6
c MLT025 Multiple Endocrine Neoplasia Iib 49 17.063
7
CNT097 Central Hypoventilation Syndrome, Congenital 54 15.797
8
P RNL100 Renal Hypodysplasia/aplasia 1 50 15.797
9
P CLR023 Colorectal Cancer 91 14.421
10
P NRF002 Neurofibromatosis 59 14.421
11
P HYP069 Hyperparathyroidism 54 14.421
12
ADN018 Adenoma 53 14.421
13
P MLT074 Multiple Endocrine Neoplasia 43 14.421
14
PHC013 Phaeochromocytoma 41 14.421
15
VNH007 Von Hippel-Lindau Syndrome 65 12.898
16
P ADN016 Adenocarcinoma 59 12.898
17
P WRD001 Waardenburg's Syndrome 51 12.898
18
THY103 Thyroid Cancer, Monmedullary, 1 50 12.898
19
c PRM005 Primary Hyperparathyroidism 48 12.898
20
CNS004 Constipation 46 12.898
21
PPL002 Papillary Carcinoma 45 12.898
22
P PRG013 Paraganglioma 44 12.898
23
END035 Endocrine Gland Cancer 41 12.898
24
P CWD001 Cowden Disease 61 11.170
25
c MLT136 Multiple Endocrine Neoplasia 1 61 11.170
26
P THY102 Thyroid Cancer, Nonmedullary, 2 53 11.170
27
HSH003 Hashimoto Thyroiditis 52 11.170
28
ACH005 Achalasia 50 11.170
29
P THY032 Thyroiditis 49 11.170
30
PLM010 Pulmonary Edema 45 11.170
31
NRM004 Neuroma 44 11.170
32
P INT070 Intestinal Obstruction 44 11.170
33
P HYP009 Hypertrophic Pyloric Stenosis 42 11.170
34
P PRT029 Parathyroid Adenoma 41 11.170
35
PRT030 Parathyroid Gland Disease 40 11.170
36
PYL006 Pyloric Stenosis 39 11.170
37
c INT072 Intestinal Pseudo-Obstruction 39 11.170
38
P HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 38 11.170
39
FLL031 Follicular Adenoma 35 11.170
40
NDL007 Nodular Goiter 35 11.170
41
GNG002 Ganglioneuroma 33 11.170
42
SHP002 Shprintzen-Goldberg Syndrome 56 9.120
43
c PRM126 Primary Peritoneal Carcinoma 47 9.120
44
MGC001 Megacolon 45 9.120
45
PRG097 Paragangliomas 1, with or Without Deafness 42 9.120
46
CLN019 Colonic Disease 42 9.120
47
c WRD020 Waardenburg Syndrome, Type 4a 41 9.120
48
P PTT002 Potter's Syndrome 39 9.120
49
PRT009 Parotid Gland Cancer 38 9.120
50
SHL001 Shoulder Impingement Syndrome 37 9.120
51
ADN010 Adenosquamous Cell Lung Carcinoma 37 9.120
52
HYP108 Hyperparathyroidism-Jaw Tumor Syndrome 36 9.120
53
LRN001 Laurence-Moon Syndrome 36 9.120
54
LCH003 Lichen Nitidus 35 9.120
55
PSD008 Pseudopapilledema 35 9.120
56
P STR021 Struma Ovarii 34 9.120
57
TXC001 Toxic Megacolon 34 9.120
58
P RNL059 Renal-Hepatic-Pancreatic Dysplasia 34 9.120
59
c SPR094 Sporadic Pheochromocytoma 34 9.120
60
APP009 Appendix Adenocarcinoma 33 9.120
61
FML029 Familial Renal Papillary Carcinoma 32 9.120
62
ATS009 Autosomal Genetic Disease 31 9.120
63
c BNG029 Benign Struma Ovarii 29 9.120
64
PRS123 Persistent Generalized Lymphadenopathy 29 9.120
65
BRS032 Breast Papillary Carcinoma 29 9.120
66
ADR014 Adrenal Medulla Cancer 28 9.120
67
c MLG059 Malignant Struma Ovarii 28 9.120
68
LCH014 Lichen Amyloidosis 28 9.120
69
EXT054 Extra-Adrenal Pheochromocytoma 26 9.120
70
NRN029 Neuronal Intestinal Dysplasia 23 9.120
71
OVR109 Ovarian Germ Cell Teratoma 23 9.120
72
THY104 Thyroid Carcinoma Somatic 20 9.120
73
THY049 Thyroid Cancer, Anaplastic 18 9.120
74
MLT011 Multiple Mucosal Neuroma 18 9.120
75
P INT068 Intestinal Disease 49 6.449
76
DFF036 Differentiated Thyroid Carcinoma 45 6.449
77
P ORG009 Organ System Cancer 37 6.449
78
c CLL012 Cell Type Benign Neoplasm 35 6.449
79
c CTR103 Cataract 4, Multiple Types 34 6.449
80
ATS008 Autosomal Dominant Disease 34 6.449
81
ADR040 Adrenal Gland Pheochromocytoma 24 6.449
82
RNL105 Renal Agenesis, Unilateral 19 6.449
83
CTR009 Cataract Congenital Dominant Non Nuclear 19 6.449
84
c RTR014 Ret-Related Hirschsprung Disease 6 6.449
85
c RTR015 Ret-Related Pheochromocytoma 5 6.449