Search results for AT 101

218 hits were found for AT 101

# Family MCID Name MIFTS Score
1
BRS047 Breast Cancer 100 0.155
2
HPT021 Hepatitis 75 0.153
3
ADN016 Adenocarcinoma 70 0.149
4
LKM002 Leukemia 72 0.140
5
LYM118 Lymphoma 70 0.137
6
DPR016 Depression 73 0.136
7
SCH015 Schizophrenia 70 0.129
8
LYM031 Lymphocytic Leukemia 61 0.124
9
CLR023 Colorectal Cancer 99 0.122
10
OVR042 Ovarian Cancer 83 0.116
11
PRS040 Prostate Cancer 94 0.115
12
KDN018 Kidney Disease 68 0.114
13
MYL069 Myeloma, Multiple 85 0.113
14
PSY004 Psychotic Disorder 72 0.111
15
SRC014 Sarcoma 70 0.110
16
LNG032 Lung Cancer 99 0.109
17
THR024 Thrombosis 63 0.106
18
SQM006 Squamous Cell Carcinoma 59 0.106
19
MLN008 Melanoma 63 0.105
20
ACQ007 Acquired Immunodeficiency Syndrome 63 0.104
21
MNT002 Mental Depression 62 0.102
22
VRL011 Viral Infectious Disease 72 0.101
23
HPT023 Hepatocellular Carcinoma 98 0.100
24
LNG099 Lung Disease 67 0.096
25
LYM019 Lymphosarcoma 56 0.094
26
THL005 Thalassemia 65 0.094
27
c MNT224 Mental Retardation, X-Linked 101 19 0.093
28
MDD011 Mood Disorder 62 0.091
29
KDN017 Kidney Cancer 59 0.090
30
IMM136 Immune System Disease 49 0.090
31
GST053 Gastric Cancer 79 0.089
32
LKM062 Leukemia, Acute Lymphoblastic 68 0.089
33
DRM006 Dermatitis 68 0.088
34
MJR001 Major Depressive Disorder 66 0.085
35
HMN044 Human Immunodeficiency Virus Type 1 74 0.085
36
LVR013 Liver Disease 75 0.084
37
GRN037 Granulomatosis with Polyangiitis 68 0.081
38
c CNT035 Central Nervous System Disease 62 0.081
39
c LKM071 Leukemia, Chronic Lymphocytic 77 0.080
40
ESP021 Esophageal Cancer 83 0.080
41
HYP061 Hypertrophic Cardiomyopathy 58 0.079
42
c LKM004 Leukemia, B-Cell, Chronic 37 0.079
43
NRV007 Nervous System Disease 69 0.078
44
CRV035 Cervical Cancer 76 0.077
45
BCL006 B-Cell Lymphomas 65 0.076
46
LYN001 Lynch Syndrome 71 0.075
47
c HPT007 Hepatitis E 56 0.075
48
MNN013 Meningitis 71 0.074
49
BRN106 Burns 55 0.074
50
CYS001 Cystic Fibrosis 83 0.073
51
URN009 Urinary System Disease 49 0.072
52
GLM045 Glioma 55 0.071
53
ART023 Arthropathy 64 0.070
54
TRC086 Trichohepatoenteric Syndrome 1 51 0.070
55
ETN001 Eating Disorder 64 0.070
56
GLB002 Glioblastoma 74 0.069
57
CLF001 Cleft Lip 56 0.069
58
ENC004 Encephalitis 66 0.068
59
OPN001 Open-Angle Glaucoma 53 0.068
60
c OVR114 Ovarian Cancer 1 62 0.068
61
STR020 Strabismus 56 0.067
62
ADM013 Adamantinoma of Long Bones 48 0.067
63
HYP086 Hypothyroidism 63 0.066
64
c BTT014 Beta-Thalassemia 71 0.066
65
c GLC092 Glaucoma, Primary Open Angle 58 0.065
66
HML002 Hemolytic Anemia 63 0.065
67
CRB086 Cerebral Aneurysms 44 0.065
68
FLL037 Follicular Lymphoma 71 0.065
69
CNJ013 Conjunctivitis 63 0.064
70
NSP012 Nasopharyngeal Carcinoma 65 0.064
71
c LKM056 Leukemia, Chronic Lymphocytic 2 66 0.064
72
MSC005 Muscular Dystrophy 66 0.063
73
KRT006 Keratoconjunctivitis 54 0.062
74
DFF005 Diffuse Large B-Cell Lymphoma 56 0.062
75
HMT018 Hematopoietic Stem Cell Transplantation 58 0.062
76
AST007 Astrocytoma 49 0.062
77
OVR063 Overnutrition 48 0.061
78
THY028 Thyroid Cancer 71 0.060
79
TRN044 Transposition of the Great Arteries 41 0.060
80
SFT003 Soft Tissue Sarcoma 56 0.060
81
CRN024 Corneal Disease 44 0.060
82
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.060
83
c LRG017 Large Intestine Cancer 59 0.059
84
SNS001 Sensorineural Hearing Loss 58 0.059
85
VSC011 Vasculitis 66 0.059
86
c ACT073 Acute Leukemia 61 0.059
87
ART016 Aortic Aneurysm 70 0.058
88
PRD008 Periodontitis 66 0.058
89
PRS042 Prostate Disease 42 0.058
90
ACR007 Acromegaly 71 0.058
91
SPN046 Spinal Muscular Atrophy 66 0.058
92
ART002 Arts Syndrome 54 0.058
93
HRN028 Horns in Sheep 22 0.057
94
END044 Endometriosis 65 0.057
95
SZR006 Seizure Disorder 58 0.057
96
MSC003 Muscular Atrophy 55 0.057
97
DRY001 Dry Eye Syndrome 53 0.056
98
ANR007 Anorexia Nervosa 68 0.055
99
MYL005 Myelofibrosis 69 0.055
100
TND004 Tendinopathy 44 0.055
101
CRT013 Carotid Stenosis 53 0.054
102
XP2001 Xp22.3 Microdeletion Syndrome 25 0.054
103
KRT001 Keratoconjunctivitis Sicca 60 0.054
104
CNJ012 Conjunctival Disease 44 0.054
105
LCR008 Lacrimal Apparatus Disease 41 0.054
106
MCP006 Mucoepidermoid Carcinoma 52 0.054
107
PRD007 Periodontal Disease 65 0.053
108
HMN010 Hemangioma 60 0.053
109
LYM067 Lymphoid Leukemia 43 0.053
110
CHL067 Cholecystitis 58 0.053
111
INT066 Interstitial Lung Disease 63 0.052
112
GNT008 Giant Cell Tumor 49 0.052
113
DBL004 Double Discordia 25 0.052
114
CRB011 Cerebrotendinous Xanthomatosis 62 0.052
115
c PRG042 Progressive Familial Heart Block, Type Ia 60 0.052
116
PTY003 Pityriasis Rubra Pilaris 50 0.052
117
c BPL002 Bipolar I Disorder 50 0.052
118
SMN007 Seminoma 47 0.052
119
MYS005 Myositis 64 0.051
120
CHR072 Chordoma 64 0.051
121
CHN012 Chondrosarcoma 58 0.051
122
BRS090 Breast Reconstruction 43 0.051
123
CNG134 Congenitally Corrected Transposition of the Great Arteries 32 0.051
124
HYP265 Hypotonia 41 0.051
125
NTR005 Nutritional Deficiency Disease 58 0.050
126
HMP005 Hemiplegia 56 0.050
127
MYM013 Moyamoya Disease 1 52 0.050
128
DRM010 Dermatomyositis 66 0.049
129
PRD006 Prader-Willi Syndrome 63 0.049
130
FNC043 Fanconi Anemia, Complementation Group E 54 0.049
131
ART153 Arthrochalasia Ehlers-Danlos Syndrome 24 0.048
132
JPN002 Japanese Encephalitis 60 0.048
133
PNL012 Penile Cancer 57 0.048
134
PLM017 Pulmonary Alveolar Microlithiasis 51 0.048
135
KRT020 Keratoconus Posticus Circumscriptus 31 0.048
136
c ART138 Aortic Aneurysm, Familial Abdominal, 1 65 0.047
137
CHL068 Cholestasis 60 0.047
138
HYP035 Hypophosphatasia 59 0.047
139
IMP005 Impotence 57 0.047
140
PLL012 Pollen Allergy 51 0.047
141
c HYD064 Hydrocephalus, Congenital, 1 46 0.047
142
HMF004 Hemifacial Spasm 42 0.047
143
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 35 0.047
144
CRN036 Craniopharyngioma 66 0.047
145
NRM004 Neuroma 49 0.047
146
PRX014 Proximal Spinal Muscular Atrophy 46 0.047
147
c BRS110 Breast-Ovarian Cancer, Familial 1 38 0.046
148
GNT033 Genetic Prion Diseases 30 0.046
149
c MLG079 Malignant Pleural Mesothelioma 44 0.046
150
KRT047 Keratosis Pilaris Atrophicans 29 0.046
151
FLL027 Fallopian Tube Carcinoma 63 0.046
152
OPT003 Opiate Dependence 55 0.046
153
ECT006 Ectodermal Dysplasia 61 0.045
154
MCR141 Mucormycosis 49 0.045
155
HDG002 Hodgkin\'s Lymphoma, Lymphocytic-Histiocytic Predominance 47 0.045
156
BNN005 Bunion 33 0.045
157
CMM004 Common Variable Immunodeficiency 71 0.044
158
MST009 Mastocytosis 63 0.044
159
OVR046 Ovarian Cyst 53 0.044
160
SPL018 Splenomegaly 45 0.044
161
CMP010 Complex Regional Pain Syndrome 62 0.043
162
GST037 Gastroparesis 59 0.043
163
CYS008 Cystic Echinococcosis 48 0.043
164
PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.043
165
THR013 Thoracic Outlet Syndrome 55 0.042
166
MCR004 Macroglobulinemia 53 0.042
167
CYS009 Cystadenoma 42 0.042
168
VRR004 Verrucous Carcinoma 55 0.041
169
HMG002 Hemoglobinuria 51 0.041
170
RGH001 Right Bundle Branch Block 45 0.041
171
PLS016 Plasma Cell Leukemia 43 0.041
172
TRC062 Tricuspid Atresia 41 0.041
173
MST019 Mastoiditis 34 0.041
174
ACN002 Acanthosis Nigricans 66 0.040
175
BNG032 Benign Mesothelioma 47 0.040
176
IMM003 Immunoglobulin Alpha Deficiency 47 0.040
177
c PRG043 Progressive Familial Heart Block, Type Ib 45 0.040
178
ATX010 Ataxia Neuropathy Spectrum 32 0.040
179
LMB006 Limb-Girdle Muscular Dystrophy 55 0.039
180
CYS010 Cystinosis 55 0.039
181
CLC001 Calciphylaxis 53 0.039
182
PSD007 Pseudomyxoma Peritonei 53 0.039
183
CPL006 Capillary Hemangioma 52 0.039
184
CRN017 Coronary Thrombosis 48 0.039
185
GLT009 Gelatinous Ascites 22 0.039
186
PND002 Pendred Syndrome 59 0.038
187
DBN001 Dubin-Johnson Syndrome 58 0.038
188
PHH001 Phaeohyphomycosis 49 0.038
189
c ADN012 Adenocarcinoma in Situ 40 0.038
190
BNG018 Benign Paroxysmal Positional Nystagmus 39 0.038
191
MYS001 Myositis Ossificans 39 0.038
192
EPD005 Epidural Abscess 36 0.038
193
c MLT010 Multiple Personality Disorder 33 0.038
194
GST007 Gastric Dilatation 31 0.038
195
ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 70 0.036
196
MLN066 Melanoma, Cutaneous Malignant 1 66 0.036
197
ANR048 Aniridia 1 65 0.036
198
PTT014 Pitt-Hopkins Syndrome 54 0.036
199
ESN020 Eosinophilic Granulomatosis with Polyangiitis 54 0.036
200
CYS036 Cystinosis, Nephropathic 52 0.036
201
ADP007 Adie Pupil 43 0.036
202
PRS123 Persistent Generalized Lymphadenopathy 39 0.036
203
VRT013 Vertigo, Benign Recurrent 37 0.036
204
NCR001 Necrotizing Ulcerative Gingivitis 36 0.036
205
EXF003 Exfoliative Dermatitis 28 0.036
206
BLD137 Blood Group--Ahonen 24 0.036
207
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 46 0.034
208
c NNS007 Nonsyndromic Deafness 46 0.034
209
c BRN108 Branchiootic Syndrome 1 45 0.034
210
CNT046 Central Nervous System Vasculitis 43 0.034
211
EXC002 Exocrine Pancreatic Insufficiency 40 0.034
212
STT004 Steatorrhea 40 0.034
213
ANK008 Ankyloglossia 39 0.034
214
C3G002 C3 Glomerulopathy 37 0.034
215
END075 Endocervical Adenocarcinoma 37 0.034
216
ACT232 Acute Necrotizing Encephalopathy 33 0.034
217
c ATS006 Autosomal Recessive Nonsyndromic Deafness 30 0.034
218
HLS001 Heel Spur 27 0.034
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