Search results for "[genes] RET"

40 hits were found for '[genes] RET'

# Family MCID Name MIFTS Score
1
P MDL022 Medullary Thyroid Carcinoma, Familial 48 68.773
2
c MLT024 Multiple Endocrine Neoplasia Iia 49 55.698
3
P HRS035 Hirschsprung Disease 1 58 28.526
4
P PHC003 Pheochromocytoma 79 22.552
5
c MLT025 Multiple Endocrine Neoplasia Iib 34 22.552
6
P MLT074 Multiple Endocrine Neoplasia 53 20.171
7
THY028 Thyroid Cancer 63 17.468
8
CNT097 Central Hypoventilation Syndrome, Congenital 58 17.468
9
P NRF002 Neurofibromatosis 69 14.263
10
P CWD001 Cowden Disease 69 14.263
11
P WRD001 Waardenburg's Syndrome 57 14.263
12
P HYP069 Hyperparathyroidism 57 14.263
13
PPL002 Papillary Carcinoma 49 14.263
14
P PRG013 Paraganglioma 46 14.263
15
P HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 41 14.263
16
UNL007 Unilateral Renal Agenesis 38 12.352
17
THY095 Thyroid Carcinoma, Follicular 55 10.085
18
P INT070 Intestinal Obstruction 53 10.085
19
c PRM126 Primary Peritoneal Carcinoma 53 10.085
20
P PRM001 Primary Cutaneous Amyloidosis 50 10.085
21
MDL009 Medullary Sponge Kidney 48 10.085
22
PNC053 Pancreatic Islet Cell Tumors 46 10.085
23
RNL078 Renal Dysplasia 46 10.085
24
P RNL100 Renal Hypodysplasia/aplasia 1 44 10.085
25
MYX014 Myxoid/round Cell Liposarcoma 43 10.085
26
SCR024 Sacrococcygeal Teratoma 40 10.085
27
FLL031 Follicular Adenoma 39 10.085
28
P STR021 Struma Ovarii 39 10.085
29
P PRT070 Peritoneal Carcinoma 39 10.085
30
PRT030 Parathyroid Gland Disease 31 10.085
31
HYP572 Hypoganglionosis 25 10.085
32
c FML143 Familial Papillary Thyroid Carcinoma 12 10.085
33
CRV067 Cervical Neuroblastoma 12 10.085
34
P NRB001 Neuroblastoma 68 7.131
35
P THY094 Thyroid Carcinoma, Papillary 46 7.131
36
ADR040 Adrenal Gland Pheochromocytoma 28 7.131
37
CTR009 Cataract Congenital Dominant Non Nuclear 27 7.131
38
c RTR014 Ret-Related Hirschsprung Disease 6 7.131
39
c RTR015 Ret-Related Pheochromocytoma 5 7.131
40
c RTR016 Ret-Related Renal Adysplasia 4 7.131