Search results for ache

186 hits were found for ache

# Family MCID Name MIFTS Score
1
ACH004 Achondroplasia 66 5.653
2
DMN002 Dementia 65 3.554
3
P MYS003 Myasthenia Gravis 67 3.515
4
P HRS035 Hirschsprung Disease 1 58 3.515
5
P PLY019 Polyneuropathy 56 3.515
6
P CNG001 Congenital Myasthenic Syndrome 55 3.515
7
VSC002 Vascular Dementia 54 3.515
8
P ALZ034 Alzheimer Disease 92 3.187
9
c MYS051 Myasthenic Syndrome, Congenital, 5 40 3.187
10
MLR004 Malaria 83 3.144
11
NRL016 Neural Tube Defects 76 3.144
12
CRB039 Cerebrovascular Disease 63 3.144
13
P DMN033 Dementia, Frontotemporal 62 3.144
14
DMN031 Dementia, Lewy Body 58 3.144
15
P INT070 Intestinal Obstruction 57 3.144
16
P SPR098 Supranuclear Palsy, Progressive 56 3.144
17
GST009 Gastroschisis 47 3.144
18
MGC001 Megacolon 45 3.144
19
WRN002 Wernicke-Korsakoff Syndrome 44 3.144
20
AMN003 Amnestic Disorder 43 3.144
21
CLN006 Colonic Pseudo-Obstruction 31 3.144
22
c PTS008 Ptosis, Congenital 31 3.144
23
P ORT004 Orthostatic Intolerance 64 2.722
24
ANN002 Anencephaly 54 2.722
25
PRT058 Pure Autonomic Failure 52 2.722
26
P APL006 Aplasia Cutis Congenita 52 2.722
27
TXC002 Toxic Encephalopathy 51 2.722
28
CLN019 Colonic Disease 51 2.722
29
BNS003 Binswanger's Disease 42 2.722
30
RMS001 Rem Sleep Behavior Disorder 41 2.722
31
ATN011 Autoinflammation with Infantile Enterocolitis 39 2.722
32
TND006 Tendinosis 38 2.722
33
HYP022 Hypohidrosis 37 2.722
34
MYP100 Myopathy, X-Linked, with Excessive Autophagy 37 2.722
35
AGR018 Agraphia 36 2.722
36
NRM006 Neuromuscular Junction Disease 35 2.722
37
RMN001 Rumination Disorder 34 2.722
38
NMN001 Nominal Aphasia 33 2.722
39
IRN007 Irinotecan Toxicity 30 2.722
40
CHL035 Cholinergic Urticaria 29 2.722
41
HYP572 Hypoganglionosis 29 2.722
42
CNG116 Congenital Nephrotic Syndrome Finnish Type 28 2.722
43
NRN029 Neuronal Intestinal Dysplasia 18 2.722
44
PRM227 Primary Orthostatic Hypotension 18 2.722
45
c CNT035 Central Nervous System Disease 60 2.254
46
P NRV007 Nervous System Disease 71 2.223
47
EPD045 Epidermolysis Bullosa, Junctional, with Pyloric Stenosis 46 2.223
48
EPD061 Epidermolysis Bullosa, Junctional, Herlitz Type 38 2.223
49
c CTR118 Cataract 14, Multiple Types 37 2.223
50
c CTR098 Cataract 1, Multiple Types 37 2.223
51
NRN002 Neuronitis 41 0.145
52
P MMP001 Mumps 58 0.097
53
BCK006 Back Pain 43 0.097
54
PHL003 Phlebotomus Fever 33 0.097
55
AVN001 Avian Influenza 54 0.084
56
EHR002 Ehrlichiosis 38 0.084
57
WST003 West Nile Fever 34 0.084
58
LYM017 Lyme Disease 63 0.069
59
HYP066 Hyperglycemia 61 0.069
60
c SVR001 Severe Acute Respiratory Syndrome 57 0.069
61
NRM005 Neuromuscular Disease 56 0.069
62
c PND001 Pain Disorder 54 0.069
63
SPT005 Spotted Fever 53 0.069
64
PLG002 Plague 51 0.069
65
HMN014 Human Immunodeficiency Virus Infectious Disease 50 0.069
66
VCC001 Vaccinia 46 0.069
67
LYM009 Lymphocytic Choriomeningitis 43 0.069
68
INH001 Inhalation Anthrax 42 0.069
69
EBL001 Ebola Hemorrhagic Fever 40 0.069
70
ACR005 Acrodermatitis 36 0.069
71
GLN002 Glanders 35 0.069
72
MNK002 Monkeypox 35 0.069
73
HMN002 Human Granulocytic Anaplasmosis 33 0.069
74
HMN001 Human Monocytic Ehrlichiosis 24 0.069
75
MYS045 Myasthenia, Congenital, 12, with Tubular Aggregates 23 0.069
76
BRZ001 Brazilian Hemorrhagic Fever 14 0.069
77
GST018 Gastrointestinal Tularemia 11 0.069
78
P BRS047 Breast Cancer 100 0.048
79
P HPT023 Hepatocellular Carcinoma 92 0.048
80
P HYP607 Hypercholesterolemia, Familial 76 0.048
81
P CRN211 Coronary Artery Disease 74 0.048
82
P RTN024 Retinoblastoma 74 0.048
83
P INF038 Influenza 72 0.048
84
P PLM036 Pulmonary Fibrosis 71 0.048
85
P LKM002 Leukemia 71 0.048
86
P ADN016 Adenocarcinoma 69 0.048
87
P HPT021 Hepatitis 69 0.048
88
P GLB002 Glioblastoma 68 0.048
89
PSY004 Psychotic Disorder 67 0.048
90
CHG001 Chagas Disease 67 0.048
91
P MNN013 Meningitis 67 0.048
92
P ATR011 Atrial Fibrillation 66 0.048
93
P EPL164 Epilepsy 66 0.048
94
P MSC005 Muscular Dystrophy 65 0.048
95
P BPL003 Bipolar Disorder 62 0.048
96
P LYM026 Lymphoblastic Leukemia 62 0.048
97
P TXP001 Toxoplasmosis 61 0.048
98
P ANR007 Anorexia Nervosa 61 0.048
99
MDD011 Mood Disorder 61 0.048
100
P CLR108 Colorectal Adenoma 60 0.048
101
c ATM011 Autoimmune Hepatitis 60 0.048
102
c MCP004 Mucopolysaccharidosis Iv 60 0.048
103
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.048
104
CNT097 Central Hypoventilation Syndrome, Congenital 59 0.048
105
P NRP001 Neuropathy 59 0.048
106
LPD008 Lipid Metabolism Disorder 58 0.048
107
PPT005 Peptic Ulcer Disease 58 0.048
108
TRG002 Trigeminal Neuralgia 57 0.048
109
P RBL001 Rubella 57 0.048
110
TNS005 Tonsillitis 57 0.048
111
INT002 Intermittent Claudication 56 0.048
112
c HYP615 Hyperparathyroidism, Familial Primary 56 0.048
113
ART111 Artery Disease 55 0.048
114
CCC001 Coccidioidomycosis 55 0.048
115
RHM001 Rheumatic Fever 54 0.048
116
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 53 0.048
117
WST005 West Nile Virus 53 0.048
118
SLP005 Sleep Disorder 53 0.048
119
P SYP003 Syphilis 53 0.048
120
DSS008 Disease of Mental Health 52 0.048
121
OST015 Osteochondrodysplasia 52 0.048
122
HNT002 Hantavirus Pulmonary Syndrome 51 0.048
123
GNR004 Generalized Anxiety Disorder 51 0.048
124
P PLY017 Polyarteritis Nodosa 51 0.048
125
STM006 Stomach Disease 50 0.048
126
CLN015 Colon Adenocarcinoma 50 0.048
127
P HYP614 Hyperlipidemia, Familial Combined 50 0.048
128
PLR008 Pleurisy 50 0.048
129
P CNG046 Congenital Fiber-Type Disproportion 50 0.048
130
BRX001 Bruxism 49 0.048
131
SRT004 Serotonin Syndrome 49 0.048
132
LMB002 Lambert-Eaton Myasthenic Syndrome 49 0.048
133
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.048
134
P FML035 Familial Hyperlipidemia 48 0.048
135
MTB004 Metabolic Acidosis 48 0.048
136
DWR001 Dwarfism 47 0.048
137
c SPR009 Sporadic Breast Cancer 47 0.048
138
BRD001 Brody Myopathy 47 0.048
139
PST095 Post-Thrombotic Syndrome 47 0.048
140
SKL014 Skeletal Dysplasia 46 0.048
141
SCR002 Scurvy 46 0.048
142
ATN004 Autonomic Neuropathy 45 0.048
143
ACD009 Acid-Labile Subunit, Deficiency of 45 0.048
144
SKL017 Skeletal Dysplasias 45 0.048
145
VTM002 Vitamin B12 Deficiency 44 0.048
146
DNG001 Dengue Shock Syndrome 43 0.048
147
CRT015 Carotid Artery Occlusion 43 0.048
148
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 43 0.048
149
HYP017 Hypophosphatemia 43 0.048
150
BHR001 Behr Syndrome 42 0.048
151
END072 Endotheliitis 42 0.048
152
GLC008 Glucose Metabolism Disease 42 0.048
153
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.048
154
P MYF003 Myofibrillar Myopathy 42 0.048
155
PNM013 Pneumococcal Meningitis 41 0.048
156
c SCN006 Secondary Syphilis 41 0.048
157
c SBC007 Subacute Thyroiditis 40 0.048
158
BND014 Bone Development Disease 40 0.048
159
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 39 0.048
160
HPT004 Hepatic Coma 39 0.048
161
P MXL015 Maxillary Sinusitis 38 0.048
162
LGN004 Legionaire Disease 38 0.048
163
DRG001 Drug Psychosis 38 0.048
164
HYP189 Hypoadrenalism 37 0.048
165
BNS002 Bone Structure Disease 37 0.048
166
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 36 0.048
167
SPN185 Spinal Cord Infarction 34 0.048
168
ACR002 Acrocapitofemoral Dysplasia 33 0.048
169
c HYP272 Hypercholesterolemia, Familial, 3 32 0.048
170
PNT001 Pontiac Fever 32 0.048
171
c MYS058 Myasthenic Syndrome, Congenital, 13, with Tubular Aggregates 32 0.048
172
PRS037 Periostitis 30 0.048
173
c CNT068 Central Pain Syndrome 29 0.048
174
PHS010 Phosphoglycerate Mutase Deficiency 26 0.048
175
PRF003 Piriformis Syndrome 26 0.048
176
c SPN098 Spinocerebellar Ataxia 25 25 0.048
177
CNT067 Central Cord Syndrome 23 0.048
178
BRR001 Barre-Lieou Syndrome 16 0.048
179
MYP071 Myopathy Due to Myoadenylate Deaminase Deficiency 16 0.048
180
LVT001 Levator Syndrome 15 0.048
181
STT044 Statin Toxicity 14 0.048
182
CHR280 Chronic Erosive Gastritis 13 0.048
183
MLL006 Mollaret Meningitis 12 0.048
184
CNT066 Central Cervical Cord Syndrome 11 0.048
185
TRC088 Trochleitis 10 0.048
186
ERY018 Erythema Nodosum, Idiopathic 5 0.048
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