Search results for ache

188 hits were found for ache

# Family MCID Name MIFTS Score
1
ACH004 Achondroplasia 66 5.664
2
P MYS003 Myasthenia Gravis 67 3.119
3
CRB039 Cerebrovascular Disease 63 3.119
4
P HRS035 Hirschsprung Disease 1 58 3.119
5
P CNG001 Congenital Myasthenic Syndrome 54 3.119
6
P PLY019 Polyneuropathy 54 3.119
7
VSC002 Vascular Dementia 52 3.119
8
c MYS051 Myasthenic Syndrome, Congenital, 5 45 2.770
9
P ALZ034 Alzheimer Disease 76 2.750
10
DMN002 Dementia 52 2.750
11
MLR004 Malaria 82 2.701
12
NRL016 Neural Tube Defects 76 2.701
13
P DMN033 Dementia, Frontotemporal 65 2.701
14
DMN031 Dementia, Lewy Body 59 2.701
15
P SPR098 Supranuclear Palsy, Progressive 59 2.701
16
P INT070 Intestinal Obstruction 55 2.701
17
ANN002 Anencephaly 53 2.701
18
WRN002 Wernicke-Korsakoff Syndrome 46 2.701
19
MGC001 Megacolon 46 2.701
20
AMN003 Amnestic Disorder 43 2.701
21
GST009 Gastroschisis 40 2.701
22
CLN006 Colonic Pseudo-Obstruction 31 2.701
23
c PTS008 Ptosis, Congenital 31 2.701
24
P PRK057 Parkinson Disease, Late-Onset 68 2.205
25
P ORT004 Orthostatic Intolerance 63 2.205
26
CLN019 Colonic Disease 51 2.205
27
PRT058 Pure Autonomic Failure 50 2.205
28
TXC002 Toxic Encephalopathy 50 2.205
29
P APL006 Aplasia Cutis Congenita 48 2.205
30
EPD045 Epidermolysis Bullosa, Junctional, with Pyloric Stenosis 47 2.205
31
CNN011 Cenani-Lenz Syndactyly Syndrome 42 2.205
32
BNS003 Binswanger's Disease 40 2.205
33
EPD061 Epidermolysis Bullosa, Junctional, Herlitz Type 40 2.205
34
RMS001 Rem Sleep Behavior Disorder 40 2.205
35
MYP100 Myopathy, X-Linked, with Excessive Autophagy 39 2.205
36
TND006 Tendinosis 38 2.205
37
c CTR118 Cataract 14, Multiple Types 38 2.205
38
c CTR098 Cataract 1, Multiple Types 38 2.205
39
NRM006 Neuromuscular Junction Disease 36 2.205
40
HYP022 Hypohidrosis 36 2.205
41
AGR018 Agraphia 35 2.205
42
RMN001 Rumination Disorder 35 2.205
43
ATN011 Autoinflammation with Infantile Enterocolitis 33 2.205
44
NMN001 Nominal Aphasia 33 2.205
45
IRN007 Irinotecan Toxicity 31 2.205
46
CHL035 Cholinergic Urticaria 28 2.205
47
HYP572 Hypoganglionosis 28 2.205
48
CNG116 Congenital Nephrotic Syndrome Finnish Type 27 2.205
49
PRM227 Primary Orthostatic Hypotension 20 2.205
50
NRN029 Neuronal Intestinal Dysplasia 18 2.205
51
P NRV007 Nervous System Disease 70 1.599
52
c CNT035 Central Nervous System Disease 60 1.599
53
NRN002 Neuronitis 39 0.145
54
BCK006 Back Pain 41 0.097
55
P MMP001 Mumps 54 0.084
56
LYM017 Lyme Disease 62 0.069
57
HYP066 Hyperglycemia 59 0.069
58
NRM005 Neuromuscular Disease 55 0.069
59
AVN001 Avian Influenza 50 0.069
60
PLG002 Plague 50 0.069
61
THR013 Thoracic Outlet Syndrome 49 0.069
62
DRG001 Drug Psychosis 41 0.069
63
INH001 Inhalation Anthrax 39 0.069
64
EHR002 Ehrlichiosis 39 0.069
65
ACR005 Acrodermatitis 35 0.069
66
WST003 West Nile Fever 30 0.069
67
PHL003 Phlebotomus Fever 29 0.069
68
MYS045 Myasthenia, Congenital, 12, with Tubular Aggregates 24 0.069
69
c MYS068 Myasthenic Syndrome, Congenital, 20, Presynaptic 20 0.069
70
P BRS047 Breast Cancer 100 0.048
71
P HPT023 Hepatocellular Carcinoma 89 0.048
72
P RTN024 Retinoblastoma 75 0.048
73
P CRN211 Coronary Artery Disease 73 0.048
74
P LKM002 Leukemia 72 0.048
75
P INF038 Influenza 71 0.048
76
P ADN016 Adenocarcinoma 69 0.048
77
P HPT021 Hepatitis 68 0.048
78
P PLM036 Pulmonary Fibrosis 68 0.048
79
PSY004 Psychotic Disorder 67 0.048
80
CHG001 Chagas Disease 66 0.048
81
P GLB002 Glioblastoma 66 0.048
82
P ATR011 Atrial Fibrillation 65 0.048
83
P MNN013 Meningitis 65 0.048
84
P MSC005 Muscular Dystrophy 65 0.048
85
P EPL164 Epilepsy 65 0.048
86
P LYM026 Lymphoblastic Leukemia 60 0.048
87
P BPL003 Bipolar Disorder 60 0.048
88
c MCP004 Mucopolysaccharidosis Iv 60 0.048
89
P TXP001 Toxoplasmosis 60 0.048
90
P ANR007 Anorexia Nervosa 60 0.048
91
MDD011 Mood Disorder 59 0.048
92
P CLR108 Colorectal Adenoma 59 0.048
93
CNT097 Central Hypoventilation Syndrome, Congenital 57 0.048
94
c ATM011 Autoimmune Hepatitis 57 0.048
95
P NRP001 Neuropathy 57 0.048
96
LPD008 Lipid Metabolism Disorder 57 0.048
97
PPT005 Peptic Ulcer Disease 57 0.048
98
TRG002 Trigeminal Neuralgia 56 0.048
99
TNS005 Tonsillitis 56 0.048
100
ART111 Artery Disease 55 0.048
101
INT002 Intermittent Claudication 55 0.048
102
c PND001 Pain Disorder 55 0.048
103
RHM001 Rheumatic Fever 54 0.048
104
SLP005 Sleep Disorder 54 0.048
105
c HYP615 Hyperparathyroidism, Familial Primary 53 0.048
106
P RBL001 Rubella 53 0.048
107
c SVR001 Severe Acute Respiratory Syndrome 53 0.048
108
CCC001 Coccidioidomycosis 53 0.048
109
DSS008 Disease of Mental Health 53 0.048
110
OST015 Osteochondrodysplasia 52 0.048
111
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 52 0.048
112
P THY054 Thyrotoxic Periodic Paralysis 51 0.048
113
WST005 West Nile Virus 51 0.048
114
P SYP003 Syphilis 51 0.048
115
P PLY017 Polyarteritis Nodosa 51 0.048
116
LST001 Listeriosis 50 0.048
117
CLN015 Colon Adenocarcinoma 49 0.048
118
SPT005 Spotted Fever 49 0.048
119
P CNG046 Congenital Fiber-Type Disproportion 49 0.048
120
LGN001 Legionnaires' Disease 49 0.048
121
c HYP071 Hypersensitivity Reaction Type Ii Disease 48 0.048
122
PST095 Post-Thrombotic Syndrome 48 0.048
123
BRX001 Bruxism 48 0.048
124
LMB002 Lambert-Eaton Myasthenic Syndrome 48 0.048
125
P CHR345 Chronic Pain 48 0.048
126
PLR008 Pleurisy 47 0.048
127
STM006 Stomach Disease 47 0.048
128
MTB004 Metabolic Acidosis 47 0.048
129
HNT002 Hantavirus Pulmonary Syndrome 47 0.048
130
SRT004 Serotonin Syndrome 47 0.048
131
BBS001 Babesiosis 47 0.048
132
SKL014 Skeletal Dysplasia 46 0.048
133
c SPR009 Sporadic Breast Cancer 46 0.048
134
HMN014 Human Immunodeficiency Virus Infectious Disease 45 0.048
135
VTM002 Vitamin B12 Deficiency 45 0.048
136
DWR001 Dwarfism 45 0.048
137
GLC008 Glucose Metabolism Disease 44 0.048
138
SKL017 Skeletal Dysplasias 44 0.048
139
SCR002 Scurvy 43 0.048
140
VCC001 Vaccinia 43 0.048
141
EBL001 Ebola Hemorrhagic Fever 43 0.048
142
HYP017 Hypophosphatemia 42 0.048
143
ATN004 Autonomic Neuropathy 42 0.048
144
END072 Endotheliitis 41 0.048
145
CRT015 Carotid Artery Occlusion 41 0.048
146
PNM013 Pneumococcal Meningitis 41 0.048
147
P MYF003 Myofibrillar Myopathy 40 0.048
148
DNG001 Dengue Shock Syndrome 40 0.048
149
HPT004 Hepatic Coma 39 0.048
150
c SBC007 Subacute Thyroiditis 39 0.048
151
c SCN006 Secondary Syphilis 39 0.048
152
LYM009 Lymphocytic Choriomeningitis 39 0.048
153
BND014 Bone Development Disease 39 0.048
154
ADP001 Adiposis Dolorosa 38 0.048
155
HYP189 Hypoadrenalism 36 0.048
156
P MXL015 Maxillary Sinusitis 36 0.048
157
BNS002 Bone Structure Disease 36 0.048
158
c MYP078 Myopathy, Myofibrillar, 3 35 0.048
159
GLN002 Glanders 35 0.048
160
MNK002 Monkeypox 35 0.048
161
SPN185 Spinal Cord Infarction 33 0.048
162
c MYS058 Myasthenic Syndrome, Congenital, 13, with Tubular Aggregates 33 0.048
163
PNT001 Pontiac Fever 33 0.048
164
HMN002 Human Granulocytic Anaplasmosis 31 0.048
165
PRS037 Periostitis 30 0.048
166
c CNT068 Central Pain Syndrome 29 0.048
167
c SPN098 Spinocerebellar Ataxia 25 28 0.048
168
PHS010 Phosphoglycerate Mutase Deficiency 26 0.048
169
PRF003 Piriformis Syndrome 25 0.048
170
c THY084 Thyrotoxic Periodic Paralysis 1 23 0.048
171
c THY083 Thyrotoxic Periodic Paralysis 2 23 0.048
172
c PSD090 Pseudohypoaldosteronism, Type Iia 23 0.048
173
HMN001 Human Monocytic Ehrlichiosis 22 0.048
174
CNT067 Central Cord Syndrome 22 0.048
175
VNT030 Ventriculomegaly with Cystic Kidney Disease 21 0.048
176
MYP071 Myopathy Due to Myoadenylate Deaminase Deficiency 18 0.048
177
c MYS067 Myasthenic Syndrome, Congenital, 22 18 0.048
178
STT044 Statin Toxicity 17 0.048
179
LVT001 Levator Syndrome 15 0.048
180
CHR280 Chronic Erosive Gastritis 13 0.048
181
MLL006 Mollaret Meningitis 13 0.048
182
BRZ001 Brazilian Hemorrhagic Fever 11 0.048
183
TRC088 Trochleitis 10 0.048
184
CNT066 Central Cervical Cord Syndrome 8 0.048
185
GST018 Gastrointestinal Tularemia 8 0.048
186
BRR001 Barre-Lieou Syndrome 7 0.048
187
LYM055 Lyme Disease - Neurological Complications 5 0.048
188
ERY018 Erythema Nodosum, Idiopathic 5 0.048
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