Search results for AT 101

166 hits were found for AT 101

# Family MCID Name MIFTS Score
1
P BRS047 Breast Cancer 100 0.186
2
P LKM002 Leukemia 72 0.178
3
P LYM118 Lymphoma 70 0.162
4
P ADN016 Adenocarcinoma 70 0.151
5
P HPT021 Hepatitis 76 0.142
6
DPR016 Depression 72 0.136
7
P CLR023 Colorectal Cancer 97 0.127
8
P PRS040 Prostate Cancer 90 0.122
9
P SCH015 Schizophrenia 69 0.122
10
P PNC044 Pancreatitis 64 0.120
11
P LNG032 Lung Cancer 98 0.117
12
P KDN018 Kidney Disease 68 0.113
13
PSY004 Psychotic Disorder 71 0.113
14
SQM006 Squamous Cell Carcinoma 59 0.110
15
ACQ007 Acquired Immunodeficiency Syndrome 63 0.108
16
MNT002 Mental Depression 57 0.106
17
SRC014 Sarcoma 68 0.105
18
MLN008 Melanoma 62 0.103
19
P HPT023 Hepatocellular Carcinoma 94 0.103
20
c MNT224 Mental Retardation, X-Linked 101 19 0.102
21
URN009 Urinary System Disease 55 0.101
22
P MYC007 Myocardial Infarction 79 0.101
23
c OVR114 Ovarian Cancer 1 62 0.099
24
P INF038 Influenza 76 0.099
25
P OVR042 Ovarian Cancer 81 0.098
26
IMM136 Immune System Disease 56 0.096
27
RNL114 Renal Cell Carcinoma, Nonpapillary 59 0.096
28
GST053 Gastric Cancer 77 0.092
29
MYL069 Myeloma, Multiple 83 0.092
30
THR024 Thrombosis 61 0.091
31
ANR040 Aneurysm 60 0.091
32
LYM019 Lymphosarcoma 55 0.090
33
MDD011 Mood Disorder 63 0.089
34
P PNM007 Pneumonia 69 0.089
35
P LYM026 Lymphoblastic Leukemia 64 0.089
36
P MJR001 Major Depressive Disorder 65 0.087
37
c CNT035 Central Nervous System Disease 63 0.087
38
c LKM071 Leukemia, Chronic Lymphocytic 75 0.086
39
P LVR013 Liver Disease 75 0.084
40
P NRV007 Nervous System Disease 73 0.084
41
P THL005 Thalassemia 64 0.084
42
P KDN017 Kidney Cancer 58 0.084
43
LYM024 Lymphatic System Disease 54 0.083
44
c LKM004 Leukemia, B-Cell, Chronic 36 0.081
45
P ESP024 Esophagitis 63 0.080
46
CYS001 Cystic Fibrosis 84 0.076
47
BRN106 Burns 56 0.075
48
PDT001 Pediatric Lymphoma 45 0.075
49
P MNN013 Meningitis 70 0.074
50
c ADL001 Adult Lymphoma 39 0.074
51
P ART023 Arthropathy 67 0.073
52
CHL061 Childhood Leukemia 55 0.073
53
P HML002 Hemolytic Anemia 62 0.071
54
STR020 Strabismus 56 0.071
55
P HYP061 Hypertrophic Cardiomyopathy 64 0.070
56
DRM006 Dermatitis 66 0.070
57
P CNJ013 Conjunctivitis 63 0.069
58
P ENC004 Encephalitis 65 0.069
59
P OPN001 Open-Angle Glaucoma 51 0.068
60
c GLC092 Glaucoma, Primary Open Angle 57 0.067
61
P FLL037 Follicular Lymphoma 69 0.066
62
P MSC005 Muscular Dystrophy 66 0.065
63
KRT006 Keratoconjunctivitis 55 0.065
64
c LKM056 Leukemia, Chronic Lymphocytic 2 41 0.064
65
CRN024 Corneal Disease 47 0.064
66
TRN044 Transposition of the Great Arteries 40 0.064
67
CHL010 Childhood Kidney Cell Carcinoma 43 0.063
68
SNS001 Sensorineural Hearing Loss 56 0.063
69
c HPT007 Hepatitis E 53 0.063
70
OVR063 Overnutrition 53 0.062
71
PRS042 Prostate Disease 44 0.062
72
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.062
73
c ACT073 Acute Leukemia 60 0.061
74
SFT003 Soft Tissue Sarcoma 58 0.061
75
DRY001 Dry Eye Syndrome 51 0.061
76
SKN019 Skin Melanoma 69 0.059
77
CNJ012 Conjunctival Disease 48 0.059
78
ART016 Aortic Aneurysm 69 0.058
79
P MSC003 Muscular Atrophy 54 0.058
80
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 45 0.058
81
KRT001 Keratoconjunctivitis Sicca 62 0.058
82
LCR008 Lacrimal Apparatus Disease 44 0.058
83
c MCL042 Macular Degeneration, Age-Related, 1 84 0.058
84
P LYN001 Lynch Syndrome 71 0.058
85
P BRN120 Bronchus Cancer 49 0.058
86
P SPN046 Spinal Muscular Atrophy 63 0.056
87
LYM067 Lymphoid Leukemia 44 0.056
88
P HYP265 Hypotonia 40 0.055
89
VSC011 Vasculitis 65 0.054
90
c PNS012 Paine Syndrome 62 0.054
91
P HMN010 Hemangioma 60 0.054
92
CNG134 Congenitally Corrected Transposition of the Great Arteries 28 0.054
93
DBL004 Double Discordia 21 0.054
94
P EPN002 Ependymoma 55 0.054
95
c BTT014 Beta-Thalassemia 69 0.052
96
PRD007 Periodontal Disease 64 0.052
97
P MYS005 Myositis 63 0.052
98
TND004 Tendinopathy 46 0.052
99
P HYP035 Hypophosphatasia 58 0.052
100
P MYM013 Moyamoya Disease 1 51 0.051
101
c BRS110 Breast-Ovarian Cancer, Familial 1 37 0.051
102
GNT033 Genetic Prion Diseases 28 0.051
103
c ART138 Aortic Aneurysm, Familial Abdominal, 1 64 0.050
104
CHL068 Cholestasis 60 0.050
105
P HMF004 Hemifacial Spasm 41 0.050
106
c PRG042 Progressive Familial Heart Block, Type Ia 58 0.049
107
NRM004 Neuroma 51 0.049
108
FLL027 Fallopian Tube Carcinoma 62 0.048
109
IMP005 Impotence 55 0.048
110
c MLG074 Malignant Mesenchymoma 54 0.048
111
GNG011 Gingival Disease 49 0.048
112
ECT006 Ectodermal Dysplasia 57 0.047
113
CMM004 Common Variable Immunodeficiency 70 0.046
114
JPN002 Japanese Encephalitis 58 0.046
115
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 63 0.045
116
P PNL012 Penile Cancer 57 0.045
117
GST037 Gastroparesis 56 0.045
118
MCP006 Mucoepidermoid Carcinoma 51 0.045
119
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 27 0.045
120
TRC062 Tricuspid Atresia 46 0.045
121
PLS016 Plasma Cell Leukemia 42 0.045
122
RGH001 Right Bundle Branch Block 46 0.043
123
IMM003 Immunoglobulin Alpha Deficiency 41 0.043
124
c PRG043 Progressive Familial Heart Block, Type Ib 41 0.043
125
CMP010 Complex Regional Pain Syndrome 57 0.042
126
PSD007 Pseudomyxoma Peritonei 53 0.042
127
HMG002 Hemoglobinuria 52 0.042
128
P NGH001 Night Blindness 51 0.042
129
GLT009 Gelatinous Ascites 21 0.042
130
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 67 0.041
131
DBN001 Dubin-Johnson Syndrome 55 0.041
132
PND002 Pendred Syndrome 55 0.041
133
CYS010 Cystinosis 54 0.041
134
P LMB006 Limb-Girdle Muscular Dystrophy 54 0.041
135
HPT082 Hepatic Adenomas, Familial 53 0.041
136
CLC001 Calciphylaxis 52 0.041
137
c ADN012 Adenocarcinoma in Situ 44 0.041
138
PRX014 Proximal Spinal Muscular Atrophy 41 0.041
139
PHH001 Phaeohyphomycosis 39 0.041
140
MST019 Mastoiditis 33 0.041
141
GST007 Gastric Dilatation 33 0.041
142
EPD005 Epidural Abscess 32 0.041
143
END016 Endocervicitis 28 0.041
144
P ANR048 Aniridia 1 65 0.039
145
P MLN066 Melanoma, Cutaneous Malignant 1 59 0.039
146
P CPL006 Capillary Hemangioma 53 0.039
147
CYS036 Cystinosis, Nephropathic 48 0.039
148
MYS001 Myositis Ossificans 39 0.039
149
NCR001 Necrotizing Ulcerative Gingivitis 38 0.039
150
EXF003 Exfoliative Dermatitis 29 0.039
151
P CNG010 Congenital Stationary Night Blindness 55 0.037
152
P PTT014 Pitt-Hopkins Syndrome 51 0.037
153
P FNC043 Fanconi Anemia, Complementation Group E 51 0.037
154
CRB151 Cerebral Creatine Deficiency Syndrome 1 50 0.037
155
SXC001 Sex Cord-Gonadal Stromal Tumor 47 0.037
156
CNT046 Central Nervous System Vasculitis 45 0.037
157
c NNS007 Nonsyndromic Deafness 44 0.037
158
P ATS366 Autism X-Linked 2 43 0.037
159
EXC002 Exocrine Pancreatic Insufficiency 43 0.037
160
STT004 Steatorrhea 41 0.037
161
END075 Endocervical Adenocarcinoma 38 0.037
162
ANK008 Ankyloglossia 37 0.037
163
FNG004 Fungal Meningitis 31 0.037
164
c ATS006 Autosomal Recessive Nonsyndromic Deafness 29 0.037
165
HLS001 Heel Spur 28 0.037
166
BLD137 Blood Group--Ahonen 17 0.037
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