Search results for TTR

210 hits were found for TTR

# Family MCID Name MIFTS Score
2
CRP001 Carpal Tunnel Syndrome 67 4.454
3
P AMY004 Amyloidosis 70 4.287
4
HYP645 Hyperthyroxinemia, Dystransthyretinemic 19 3.538
5
P PLY019 Polyneuropathy 56 3.451
6
HYP029 Hyperthyroxinemia 29 2.844
7
P HRT032 Heart Disease 75 2.637
8
P RRC004 Rare Cardiomyopathy 44 2.590
9
P PNM007 Pneumonia 68 2.571
10
NTR005 Nutritional Deficiency Disease 61 2.571
11
c HRD039 Hereditary Amyloidosis 45 2.548
12
P LVR013 Liver Disease 68 2.531
13
P KDN018 Kidney Disease 70 2.508
14
c ATR087 Atrial Standstill 1 74 2.419
15
P RST002 Restrictive Cardiomyopathy 56 2.356
16
DFC004 Deficiency Anemia 75 2.279
17
PNC001 Pancytopenia 54 2.242
18
P ALZ034 Alzheimer Disease 88 2.198
19
P DMN002 Dementia 67 2.198
20
P RHM011 Rheumatoid Arthritis 80 2.172
21
MLR004 Malaria 80 2.172
22
PHN003 Phenylketonuria 75 2.172
23
P RSP003 Respiratory Failure 74 2.172
24
P HYP086 Hypothyroidism 68 2.172
25
c CHR684 Chronic Kidney Disease 66 2.172
26
LVR012 Liver Cirrhosis 63 2.172
27
ANR007 Anorexia Nervosa 63 2.172
29
AMY082 Amyloidosis, Familial Visceral 57 2.172
30
PRT038 Protein-Energy Malnutrition 54 2.172
31
P OBS001 Obstructive Jaundice 48 2.172
32
P CHR573 Choroid Plexus Cancer 45 2.172
33
ATN004 Autonomic Neuropathy 44 1.988
34
P AMY084 Amyloidosis, Finnish Type 49 1.894
35
P PRK057 Parkinson Disease, Late-Onset 76 1.831
36
P DMY001 Demyelinating Polyneuropathy 41 1.831
37
MYL069 Myeloma, Multiple 85 1.804
38
c HYP595 Hypertension, Essential 84 1.804
39
CRB039 Cerebrovascular Disease 69 1.804
40
INT323 Intraocular Pressure Quantitative Trait Locus 62 1.804
41
P DRR001 Diarrhea 57 1.804
42
P MYP006 Myopia 55 1.804
43
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 1.773
44
P HYD006 Hydrocephalus 65 1.773
45
FND001 Fundus Albipunctatus 61 1.773
46
P CTR002 Cataract 60 1.773
47
HPT019 Hepatic Encephalopathy 60 1.773
48
P BNG030 Benign Ependymoma 60 1.773
49
DCB001 Decubitus Ulcer 60 1.773
50
P SCL018 Scoliosis 60 1.773
51
P END033 Endocarditis 57 1.773
52
IRN002 Iron Metabolism Disease 57 1.773
53
PPL058 Papilloma of Choroid Plexus 57 1.773
54
P NRM002 Normal Pressure Hydrocephalus 56 1.773
55
P ART021 Arteriosclerosis 54 1.773
56
c CNT035 Central Nervous System Disease 54 1.773
57
HLL004 Hellp Syndrome 53 1.773
58
BRT005 Barth Syndrome 53 1.773
59
P SHR001 Short Bowel Syndrome 52 1.773
60
DYS015 Dysentery 50 1.773
61
P HYP058 Hypervitaminosis a 49 1.773
62
GLS007 Glossitis 47 1.773
63
c CHR096 Chronic Pulmonary Heart Disease 43 1.773
64
MLY001 Molybdenum Cofactor Deficiency 42 1.773
65
TST018 Testicular Yolk Sac Tumor 39 1.773
66
ATR073 Atrophic Glossitis 35 1.773
67
P HRD207 Hereditary Transthyretin Amyloidosis 25 1.646
68
AMY005 Amyloid Neuropathy 27 1.523
69
P PRP019 Peripheral Nervous System Disease 57 1.509
70
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 1.415
71
PRT058 Pure Autonomic Failure 59 1.396
72
RRD019 Rare Deficiency Anemia 23 1.352
73
P BRG001 Brugada Syndrome 70 1.326
74
PLS009 Plasma Cell Neoplasm 51 1.295
75
XRP001 Xerophthalmia 42 1.295
76
P RTN008 Retinitis Pigmentosa 77 1.254
77
DGR001 Digeorge Syndrome 63 1.254
78
ANL018 Analbuminemia 54 1.254
79
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 53 1.254
80
CHR100 Chronic Ulcer of Skin 53 1.254
81
P ATN002 Autonomic Nervous System Disease 52 1.254
82
MSC190 Muscular Disease 51 1.254
83
P PRC012 Pericardial Effusion 51 1.254
84
c AMY009 Amyloidosis Aa 50 1.254
85
SPN019 Spondylolisthesis 49 1.254
86
MDS022 Mediastinitis 47 1.254
87
INT010 Intracranial Embolism 46 1.254
88
MNN020 Meningococcal Infection 45 1.254
89
KWS001 Kwashiorkor 45 1.254
90
c BLC007 Bile Acid Synthesis Defect, Congenital, 1 44 1.254
91
MRS001 Marasmus 43 1.254
92
SPN029 Spondylolysis 41 1.254
93
P INT260 Intracranial Berry Aneurysm 40 1.254
94
LGN005 Ligneous Conjunctivitis 40 1.254
95
NRV004 Nerve Compression Syndrome 38 1.254
96
BLN006 Blind Loop Syndrome 37 1.254
97
PDT025 Pediatric Multiple Sclerosis 36 1.254
98
PLM180 Pulmonary Artery Disease 35 1.254
99
HRT008 Heart Conduction Disease 33 1.254
100
CCL002 Cecal Disease 32 1.254
101
P PRC050 Pericardium Disease 32 1.254
102
OVR015 Ovarian Mixed Germ Cell Neoplasm 31 1.254
103
IMM005 Immature Teratoma of Ovary 31 1.254
104
MXD001 Mixed Cerebral Palsy 31 1.254
105
BRS043 Breast Leiomyosarcoma 30 1.254
106
c CHR047 Chronic Ethmoiditis 30 1.254
107
P ACQ009 Acquired Metabolic Disease 28 1.254
108
P BNG022 Benign Pleural Mesothelioma 27 1.254
109
MDD009 Middle Ear Carcinoma 27 1.254
110
c ATS009 Autosomal Genetic Disease 27 1.254
111
c CTR125 Cataract 7 27 1.254
112
PPL013 Papillary Ependymoma 27 1.254
113
MDN002 Median Neuropathy 27 1.254
114
LPM002 Lipoma of Colon 26 1.254
115
AMY002 Amyloid Tumor 25 1.254
116
CRT011 Carotenemia 24 1.254
117
BLD003 Bladder Lateral Wall Cancer 24 1.254
118
GLL009 Gallbladder Signet Ring Cell Adenocarcinoma 23 1.254
119
c LCL003 Localized Pulmonary Fibrosis 22 1.254
120
CRB202 Cerebrovascular Benign Neoplasm 22 1.254
121
INT034 Intracranial Cavernous Angioma 21 1.254
122
LRG007 Large Intestine Lipoma 21 1.254
123
CNJ011 Conjunctival Deposit 20 1.254
124
PRP008 Parapharyngeal Meningioma 20 1.254
125
PRM123 Paramyloidosis 20 1.254
126
CHS001 Chest Wall Lipoma 19 1.254
127
ATN001 Autonomic Peripheral Neuropathy 18 1.254
128
ASY004 Asymmetric Motor Neuropathy 18 1.254
129
INT077 Intracranial Structure Hemangioma 14 1.254
130
P NRP001 Neuropathy 56 0.219
131
ATN005 Autonomic Dysfunction 47 0.147
132
CNG034 Congestive Heart Failure 70 0.130
133
WLD005 Wild Type Attr Amyloidosis 32 0.120
134
IMP005 Impotence 52 0.110
135
KRT002 Keratomalacia 48 0.110
136
P NRV007 Nervous System Disease 66 0.098
137
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 57 0.098
138
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.098
139
P SDR002 Siderosis 44 0.098
140
P DYS021 Dysautonomia 39 0.098
141
END030 End Stage Renal Failure 58 0.085
142
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.085
143
P AXN001 Axonal Neuropathy 36 0.085
144
ADL002 Adult Syndrome 69 0.069
145
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.069
146
P ATR011 Atrial Fibrillation 66 0.069
147
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.069
148
P MTR014 Motor Neuron Disease 64 0.069
149
NRM005 Neuromuscular Disease 63 0.069
150
c ALM001 Al Amyloidosis 50 0.069
151
SPR066 Superficial Siderosis 39 0.069
152
SPR032 Superficial Siderosis of the Central Nervous System 23 0.069
153
P LNG032 Lung Cancer 97 0.049
154
P OVR042 Ovarian Cancer 89 0.049
155
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.049
156
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.049
157
STR067 Stroke, Ischemic 80 0.049
158
c HYP836 Hypercholesterolemia, Familial, 1 72 0.049
159
P HNT016 Huntington Disease 71 0.049
160
P CNR004 Cone-Rod Dystrophy 2 71 0.049
161
P NRB001 Neuroblastoma 71 0.049
162
DWN001 Down Syndrome 70 0.049
163
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.049
164
P LPR021 Leprosy 3 67 0.049
165
P HYP061 Hypertrophic Cardiomyopathy 66 0.049
166
P MSC005 Muscular Dystrophy 66 0.049
167
P DBT009 Diabetes Mellitus 64 0.049
168
MSC007 Muscle Hypertrophy 63 0.049
169
NRF026 Neurofibromatosis, Type Iv, of Riccardi 63 0.049
170
P NPH012 Nephrotic Syndrome 63 0.049
171
INT002 Intermittent Claudication 61 0.049
172
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 61 0.049
173
NRL005 Neurilemmoma 60 0.049
174
P SLP005 Sleep Disorder 59 0.049
175
P SZR006 Seizure Disorder 58 0.049
176
VSL002 Visual Epilepsy 58 0.049
177
CNS004 Constipation 57 0.049
178
P UVT001 Uveitis 57 0.049
179
GST050 Gastrointestinal System Disease 56 0.049
180
c INT064 Intermediate Uveitis 55 0.049
181
NRG002 Neurogenic Bladder 54 0.049
182
P TCD001 Tic Disorder 54 0.049
183
P LTR001 Lateral Sclerosis 53 0.049
184
SNS003 Sensory Peripheral Neuropathy 53 0.049
185
P TRM003 Tremor 53 0.049
186
c PRM092 Primary Lateral Sclerosis, Adult, 1 52 0.049
187
PTH003 Pathologic Nystagmus 51 0.049
188
DBT004 Diabetic Polyneuropathy 50 0.049
189
DYS073 Dysphagia 50 0.049
190
KRT001 Keratoconjunctivitis Sicca 50 0.049
191
P MYT002 Myotonic Dystrophy 49 0.049
192
47X002 47,xyy 49 0.049
193
P OPN001 Open-Angle Glaucoma 49 0.049
194
PRS012 Pars Planitis 48 0.049
195
SXL003 Sexual Disorder 48 0.049
196
P VTR007 Vitreoretinopathy 46 0.049
197
P PLY020 Polyradiculoneuropathy 46 0.049
198
SYN036 Syncope 45 0.049
199
PRS063 Paresthesia 43 0.049
200
MCL003 Macular Holes 42 0.049
201
c GLL037 Guillain-Barre Syndrome, Familial 42 0.049
202
MNN028 Mononeuropathy of the Median Nerve, Mild 42 0.049
203
SPS019 Spastic Paraparesis 40 0.049
204
MNN017 Mononeuropathy 39 0.049
205
c CHR682 Chronic Bilirubin Encephalopathy 38 0.049
206
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.049
207
HNS001 Hansen's Disease 34 0.049
208
SLW005 Slowed Nerve Conduction Velocity, Autosomal Dominant 32 0.049
209
ARG004 Argyria 28 0.049
210
APM002 Aapoai Amyloidosis 16 0.049
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