Search results for "[genes] TTR"

75 hits were found for '[genes] TTR'

# Family MCID Name MIFTS Score
1
P AMY004 Amyloidosis 60 20.771
2
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 46 20.771
3
P CRD011 Cardiomyopathy 53 16.089
4
HYP029 Hyperthyroxinemia 28 16.089
5
P RSP003 Respiratory Failure 58 14.688
6
P PLY019 Polyneuropathy 46 14.688
7
NTR005 Nutritional Deficiency Disease 41 14.688
8
CRP017 Carpal Tunnel Syndrome, Familial 39 14.688
9
PHN003 Phenylketonuria 73 13.137
10
c CHR089 Chronic Kidney Failure 61 13.137
11
P CRB019 Cerebral Amyloid Angiopathy 56 13.137
12
OBS001 Obstructive Jaundice 40 13.137
13
PRT038 Protein-Energy Malnutrition 40 13.137
14
P CHR019 Choroid Plexus Carcinoma 38 13.137
15
c HRD039 Hereditary Amyloidosis 36 13.137
16
P ACQ009 Acquired Metabolic Disease 27 13.137
17
HYP645 Hyperthyroxinemia, Dystransthyretinemic 19 13.137
18
LPT007 Leptomeningeal Amyloidosis 12 13.137
19
P ALZ034 Alzheimer Disease 98 11.377
20
P RHM011 Rheumatoid Arthritis 88 11.377
21
CHR029 Choroid Plexus Papilloma 52 11.377
22
SHG001 Shigellosis 52 11.377
23
KRT002 Keratomalacia 49 11.377
24
P AMY082 Amyloidosis, Familial Visceral 43 11.377
25
DYS015 Dysentery 41 11.377
26
P PRP023 Peripheral Neuropathy 40 11.377
27
P RST002 Restrictive Cardiomyopathy 38 11.377
28
P DMY001 Demyelinating Polyneuropathy 36 11.377
29
GLS007 Glossitis 36 11.377
30
DCB001 Decubitus Ulcer 35 11.377
31
ATR073 Atrophic Glossitis 33 11.377
32
c HYP058 Hypervitaminosis a 31 11.377
33
TST018 Testicular Yolk Sac Tumor 31 11.377
34
AMY005 Amyloid Neuropathy 25 11.377
35
ATT014 Attrv30m Amyloidosis 15 11.377
36
ATT015 Attrv122i Amyloidosis 12 11.377
37
P NNN008 Noonan Syndrome 1 62 9.289
38
P FND001 Fundus Albipunctatus 54 9.289
39
BRT005 Barth Syndrome 53 9.289
40
PRT058 Pure Autonomic Failure 44 9.289
41
BRN106 Burns 43 9.289
42
KWS001 Kwashiorkor 37 9.289
43
XRP001 Xerophthalmia 36 9.289
44
MLY001 Molybdenum Cofactor Deficiency 36 9.289
45
c AMY009 Amyloidosis Aa 35 9.289
46
MRS001 Marasmus 35 9.289
47
P AMY084 Amyloidosis, Finnish Type 35 9.289
48
BLD009 Bladder Neck Obstruction 34 9.289
49
MNN020 Meningococcal Infection 33 9.289
50
BLP001 Blepharochalasis 33 9.289
51
AMY002 Amyloid Tumor 32 9.289
52
TRS001 Tarsal Tunnel Syndrome 32 9.289
53
CHR100 Chronic Ulcer of Skin 31 9.289
54
HYP047 Hypertropia 31 9.289
55
PRP019 Peripheral Nervous System Disease 31 9.289
56
c CHR096 Chronic Pulmonary Heart Disease 30 9.289
57
LCL004 Localized Osteosarcoma 30 9.289
58
c FML154 Familial Restrictive Cardiomyopathy 29 9.289
59
MDN001 Median Rhomboid Glossitis 29 9.289
60
PDT025 Pediatric Multiple Sclerosis 28 9.289
61
BRW004 Brown-Sequard Syndrome 28 9.289
62
ATN002 Autonomic Nervous System Disease 27 9.289
63
PPL013 Papillary Ependymoma 26 9.289
64
NRV004 Nerve Compression Syndrome 25 9.289
65
CRT011 Carotenemia 25 9.289
66
TBR007 Tuberculum Sellae Meningioma 24 9.289
67
DYS070 Dysalbuminemic Hyperthyroxinemia 22 9.289
68
TBL007 Tibial Neuropathy 22 9.289
69
SLL002 Sella Turcica Neoplasm 18 9.289
70
CNJ010 Conjunctival Degeneration 17 9.289
71
PRM123 Paramyloidosis 16 9.289
72
FML097 Familial Amyloid Cardiomyopathy 14 9.289
73
CNJ011 Conjunctival Deposit 13 9.289
74
ATN001 Autonomic Peripheral Neuropathy 12 9.289
75
FML141 Familial Oculoleptomeningeal Amyloidosis 9 9.289