Search results for "[genes] RET"

85 hits were found for '[genes] RET'

# Family MCID Name MIFTS Score
1
P HRS035 Hirschsprung Disease 1 58 22.215
2
P MDL022 Medullary Thyroid Carcinoma, Familial 62 20.280
3
P PHC003 Pheochromocytoma 72 18.139
4
c MLT024 Multiple Endocrine Neoplasia Iia 64 18.139
5
CNT097 Central Hypoventilation Syndrome, Congenital 59 15.708
6
THY028 Thyroid Cancer 71 15.708
7
c MLT025 Multiple Endocrine Neoplasia Iib 56 15.708
8
P RNL100 Renal Hypodysplasia/aplasia 1 54 15.708
9
P CLR023 Colorectal Cancer 96 14.340
10
P ADN016 Adenocarcinoma 69 14.340
11
PHC013 Phaeochromocytoma 47 14.340
12
P LNG032 Lung Cancer 92 12.826
13
VNH007 Von Hippel-Lindau Syndrome 69 12.826
14
THY103 Thyroid Cancer, Monmedullary, 1 55 12.826
15
P HYP069 Hyperparathyroidism 57 12.826
16
CNS004 Constipation 57 12.826
17
P MLT074 Multiple Endocrine Neoplasia 55 12.826
18
ADN018 Adenoma 59 12.826
19
c MLT136 Multiple Endocrine Neoplasia 1 68 11.108
20
P THY102 Thyroid Cancer, Nonmedullary, 2 60 11.108
21
P HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 41 11.108
22
ACH005 Achalasia 55 11.108
23
HSH003 Hashimoto Thyroiditis 55 11.108
24
P WRD001 Waardenburg's Syndrome 56 11.108
25
P INT070 Intestinal Obstruction 55 11.108
26
c INT072 Intestinal Pseudo-Obstruction 45 11.108
27
P HMN010 Hemangioma 62 11.108
28
c PRM005 Primary Hyperparathyroidism 56 11.108
29
P VSC005 Vesicoureteral Reflux 53 11.108
30
P PRG013 Paraganglioma 54 11.108
31
MGC001 Megacolon 50 11.108
32
P THY032 Thyroiditis 57 11.108
33
PRT029 Parathyroid Adenoma 46 11.108
34
PYL006 Pyloric Stenosis 46 11.108
35
P HYP009 Hypertrophic Pyloric Stenosis 40 11.108
36
PPL002 Papillary Carcinoma 50 11.108
37
FLL031 Follicular Adenoma 40 11.108
38
P STR021 Struma Ovarii 33 11.108
39
SHP002 Shprintzen-Goldberg Syndrome 53 9.069
40
c WRD020 Waardenburg Syndrome, Type 4a 41 9.069
41
TMR010 Tumor Predisposition Syndrome 58 9.069
42
P RNL059 Renal-Hepatic-Pancreatic Dysplasia 39 9.069
43
LRN001 Laurence-Moon Syndrome 36 9.069
44
PRT030 Parathyroid Gland Disease 49 9.069
45
MDL009 Medullary Sponge Kidney 41 9.069
46
PSD008 Pseudopapilledema 39 9.069
47
END035 Endocrine Gland Cancer 50 9.069
48
ADR014 Adrenal Medulla Cancer 38 9.069
49
APP009 Appendix Adenocarcinoma 40 9.069
50
P PTT002 Potter's Syndrome 42 9.069
51
CLN019 Colonic Disease 50 9.069
52
PRT009 Parotid Gland Cancer 42 9.069
53
DRF001 Dirofilariasis 38 9.069
54
SHL001 Shoulder Impingement Syndrome 40 9.069
55
LCH003 Lichen Nitidus 36 9.069
56
PRS123 Persistent Generalized Lymphadenopathy 33 9.069
57
EXT054 Extra-Adrenal Pheochromocytoma 35 9.069
58
BLD045 Bladder Diverticulum 31 9.069
59
c PRM126 Primary Peritoneal Carcinoma 54 9.069
60
TST043 Testicular Seminoma 41 9.069
61
FML029 Familial Renal Papillary Carcinoma 34 9.069
62
BRS032 Breast Papillary Carcinoma 35 9.069
63
ADN010 Adenosquamous Cell Lung Carcinoma 41 9.069
64
LCH014 Lichen Amyloidosis 26 9.069
65
OVR109 Ovarian Germ Cell Teratoma 29 9.069
66
PLM039 Pulmonary Neuroendocrine Tumor 42 9.069
67
HYP572 Hypoganglionosis 29 9.069
68
c MLG059 Malignant Struma Ovarii 33 9.069
69
ATS009 Autosomal Genetic Disease 38 9.069
70
NRN029 Neuronal Intestinal Dysplasia 31 9.069
71
c BNG029 Benign Struma Ovarii 26 9.069
72
MLT011 Multiple Mucosal Neuroma 19 9.069
73
FML143 Familial Papillary Thyroid Carcinoma 28 9.069
74
c SPR094 Sporadic Pheochromocytoma 34 9.069
75
THY104 Thyroid Carcinoma Somatic 22 9.069
76
P INT068 Intestinal Disease 60 6.413
77
CTR009 Cataract Congenital Dominant Non Nuclear 25 6.413
78
ADR040 Adrenal Gland Pheochromocytoma 33 6.413
79
RNL105 Renal Agenesis, Unilateral 21 6.413
80
DFF036 Differentiated Thyroid Carcinoma 49 6.413
81
ATS008 Autosomal Dominant Disease 41 6.413
82
c CLL012 Cell Type Benign Neoplasm 41 6.413
83
P ORG009 Organ System Cancer 45 6.413
84
c RTR014 Ret-Related Hirschsprung Disease 6 6.413
85
c RTR015 Ret-Related Pheochromocytoma 5 6.413