Search results for MN1

204 hits were found for MN1

# Family MCID Name MIFTS Score
1
MN1003 Mn1 C-Terminal Truncation Syndrome 26 46.143
2
MNN043 Meningioma, Familial 79 37.738
3
CBL011 Cebalid Syndrome 28 33.458
4
AST058 Astroblastoma, Mn1-Altered 6 26.390
5
CHR072 Chordoma 57 15.683
6
c LKM061 Leukemia, Acute Myeloid 83 14.792
7
AST002 Astroblastoma 34 14.663
8
RHM015 Rhombencephalosynapsis 29 13.208
9
MYX001 Myxopapillary Ependymoma 38 8.651
10
TNY001 Tanycytic Ependymoma 27 8.651
11
TNS014 Tenosynovitis 45 8.180
12
P LRG012 Large Congenital Melanocytic Nevus 47 7.819
13
FML345 Familial Expansile Osteolysis 46 7.819
14
P ATS426 Autosomal Dominant Distal Hereditary Motor Neuronopathy 33 7.819
15
c DST106 Distal Hereditary Motor Neuronopathy Type 2 41 7.819
16
INT395 Intracranial Meningioma 48 6.623
17
SCR001 Secretory Meningioma 40 6.623
18
P MYL006 Myeloid Leukemia 60 6.158
19
LYM002 Lymphoplasmacyte-Rich Meningioma 35 5.938
20
P LKM002 Leukemia 66 5.103
21
CLF027 Cleft Palate, Isolated 64 2.854
22
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 30 2.775
23
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 2.479
24
c NRF023 Neurofibromatosis, Type Ii 70 2.191
25
c ACT073 Acute Leukemia 59 2.190
26
P BNG030 Benign Ependymoma 51 2.171
27
PLY183 Polymicrogyria with or Without Vascular-Type Ehlers-Danlos Syndrome 41 2.150
28
HYP748 Hypertelorism 46 2.150
29
PLY024 Polymicrogyria 46 2.150
30
CLL010 Cellular Ependymoma 58 1.990
31
MYL009 Myelodysplastic Syndrome 67 1.922
32
P NRF002 Neurofibromatosis 60 1.795
33
RPD005 Rapidly Involuting Congenital Hemangioma 48 1.768
34
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.655
35
P CRN037 Craniosynostosis 67 1.655
36
NRF007 Neurofibroma 64 1.615
37
c DPH024 Diaphragmatic Hernia, Congenital 64 1.513
38
P HPT023 Hepatocellular Carcinoma 95 1.513
39
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 1.513
40
P ATR010 Atrial Heart Septal Defect 58 1.513
41
HPT022 Hepatoblastoma 54 1.513
42
INT276 Interatrial Communication 50 1.513
43
P CHR285 Chronic Myelomonocytic Leukemia 59 1.486
44
GLM045 Glioma 62 1.396
45
GLL048 Glial Tumor 52 1.396
47
PLM020 Pleomorphic Xanthoastrocytoma 40 1.300
48
CHR178 Chromosomal Triplication 34 1.300
49
P LKM062 Leukemia, Acute Lymphoblastic 69 1.226
50
P CTR002 Cataract 59 1.226
51
MYL031 Myeloproliferative Neoplasm 66 1.164
52
OST159 Osteogenic Sarcoma 66 1.141
53
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 1.141
54
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.117
55
P PRR016 Pierre Robin Syndrome 50 1.092
56
CLF028 Cleft Soft Palate 38 1.092
57
P GLM040 Glioma Susceptibility 1 70 1.092
58
MLG169 Malignant Astrocytoma 57 1.092
59
P MCR010 Microcephaly 59 1.092
60
ISL075 Isolated Pierre Robin Sequence 29 1.092
61
P PLC011 Pilocytic Astrocytoma 55 1.065
62
GNG004 Ganglioglioma 53 1.065
63
ACT250 Acute Megakaryocytic Leukemia 63 1.036
64
CNS022 Cns Neuroblastoma with Foxr2 Activation 10 1.005
65
EWN003 Ewing Sarcoma 70 1.005
66
P NRB001 Neuroblastoma 66 1.005
67
MNN042 Meningioma, Radiation-Induced 51 0.968
68
MLG077 Malignant Peripheral Nerve Sheath Tumor 54 0.931
69
RRS010 Rare Soft Tissue Tumor 18 0.931
70
CRP032 Corpus Callosum, Agenesis of 49 0.884
71
NRL005 Neurilemmoma 60 0.884
72
P BRS047 Breast Cancer 97 0.873
73
P PRS040 Prostate Cancer 95 0.866
74
P LNG032 Lung Cancer 98 0.866
75
P PLY014 Polycystic Kidney Disease 71 0.862
76
P END044 Endometriosis 62 0.862
77
ANP006 Anaplastic Ependymoma 46 0.832
78
P OVR042 Ovarian Cancer 88 0.713
79
P PNC035 Pancreatic Cancer 86 0.713
80
LWC002 Lowe Oculocerebrorenal Syndrome 68 0.685
81
c FNC043 Fanconi Anemia, Complementation Group E 62 0.685
82
ADP007 Adie Pupil 40 0.685
83
c BRT038 Baraitser-Winter Syndrome 1 42 0.685
84
c ATS007 Autism Spectrum Disorder 72 0.685
85
CNT109 Central Nervous System Benign Neoplasm 30 0.685
86
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.685
87
P ATS364 Autism 72 0.685
88
VSL002 Visual Epilepsy 39 0.685
89
ANG009 Angiomatous Meningioma 25 0.685
90
SPN040 Spinal Cancer 44 0.685
91
SPN021 Spinal Meningioma 43 0.685
92
P SPN039 Spinal Canal and Spinal Cord Meningioma 24 0.685
93
MCN009 Mucinous Stomach Adenocarcinoma 24 0.685
94
c CNT035 Central Nervous System Disease 53 0.685
95
SKL030 Skull Base Cancer 23 0.685
96
NRL002 Neurilemmomatosis 52 0.685
97
P SZR006 Seizure Disorder 69 0.685
98
CLR018 Clear Cell Meningioma 30 0.685
99
P SKL005 Skull Base Meningioma 27 0.685
100
P BNG002 Benign Meningioma 36 0.685
101
MNN004 Meningothelial Meningioma 25 0.685
102
TRN002 Transitional Meningioma 25 0.685
103
EXP004 Exophthalmos 50 0.685
104
PRP018 Peripheral Nerve Schwannoma 23 0.685
105
HNM002 Hinman Syndrome 26 0.685
106
AGN016 Aging 54 0.676
107
P CLR023 Colorectal Cancer 100 0.550
108
LNG039 Lung Squamous Cell Carcinoma 57 0.513
109
P SCH015 Schizophrenia 74 0.504
110
GLB002 Glioblastoma 67 0.488
111
PST092 Posttransplant Acute Limbic Encephalitis 29 0.441
112
ANP032 Anaplastic Pleomorphic Xanthoastrocytoma 16 0.416
113
IDH005 Idh-Wildtype Glioblastoma 12 0.416
114
P GST053 Gastric Cancer 82 0.362
115
P TMR010 Tumor Predisposition Syndrome 69 0.362
116
ADN011 Adenoid Cystic Carcinoma 68 0.362
117
BLD173 Bladder Small Cell Carcinoma 44 0.362
118
VNH007 Von Hippel-Lindau Syndrome 73 0.362
119
END057 Endometrial Cancer 71 0.362
120
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.362
121
c CLR087 Colorectal Cancer 12 34 0.362
122
P LNG064 Lung Cancer Susceptibility 3 70 0.362
123
GST103 Gastric Cancer, Hereditary Diffuse 68 0.362
124
ADN089 Adenosquamous Lung Carcinoma 49 0.362
125
LNG012 Lung Occult Squamous Cell Carcinoma 20 0.362
126
SML009 Small Intestine Adenocarcinoma 57 0.362
127
CLN015 Colon Adenocarcinoma 64 0.362
128
GST040 Gastric Adenocarcinoma 66 0.362
129
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 60 0.362
130
MLT003 Multilocular Clear Cell Renal Cell Carcinoma 32 0.362
131
CLR030 Clear Cell Renal Cell Carcinoma 54 0.362
132
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 0.362
133
LNG007 Lung Mixed Small Cell and Squamous Cell Carcinoma 20 0.362
134
MLT165 Multilocular Cystic Renal Neoplasm of Low Malignant Potential 28 0.362
135
c MYT020 Myotonic Dystrophy 2 57 0.360
136
P BRS044 Breast Adenocarcinoma 58 0.360
137
STM007 Stomatitis 52 0.360
138
MYT011 Myotonia 38 0.360
139
P MYT002 Myotonic Dystrophy 51 0.360
140
P SPP010 Suppressor of Tumorigenicity 3 51 0.329
141
LNG105 Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome 36 0.329
142
CLR109 Colorectal Adenocarcinoma 50 0.329
143
ALL029 Allergic Disease 61 0.329
144
P MYP004 Myopathy 67 0.294
145
MYT003 Myotonic Disease 36 0.294
146
SPL018 Splenomegaly 47 0.294
147
P RRT020 Rare Tumor 39 0.294
148
DWN001 Down Syndrome 70 0.255
149
CRB138 Core Binding Factor Acute Myeloid Leukemia 44 0.255
150
HGH043 High Grade Glioma 46 0.255
151
CHK001 Chikungunya 60 0.208
152
HLX001 Helix Syndrome 47 0.208
153
DSS032 Disease by Infectious Agent 55 0.208
154
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.208
155
BRN032 Brain Glioma 45 0.208
156
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.208
157
P SPN046 Spinal Muscular Atrophy 62 0.208
158
P LTR001 Lateral Sclerosis 58 0.208
159
P RCT021 Rectum Cancer 54 0.208
160
TXC005 Toxic Shock Syndrome 62 0.208
161
CHL149 Childhood Acute Myeloid Leukemia 42 0.208
162
P MSC003 Muscular Atrophy 52 0.208
163
P INF038 Influenza 68 0.208
164
P MSC005 Muscular Dystrophy 66 0.208
165
OCL069 Ocular Motor Apraxia 57 0.147
166
c LKM063 Leukemia, Chronic Myeloid 71 0.147
167
KSH004 Kashin-Beck Disease 37 0.147
168
LWG006 Low Grade Glioma 41 0.147
169
PLY150 Polykaryocytosis Inducer 29 0.147
170
OST006 Osteoblastoma 38 0.147
171
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.147
172
P KLZ004 Kala-Azar 1 41 0.147
173
P WSK001 Wiskott-Aldrich Syndrome 72 0.147
174
LTH043 Lithium Transport 17 0.147
175
PST113 Posterior Fossa Ependymoma 27 0.147
176
SPR168 Supratentorial Ependymoma 21 0.147
177
PNC001 Pancytopenia 52 0.147
178
PLM021 Pilomyxoid Astrocytoma 42 0.147
179
ADN009 Adenosquamous Carcinoma 49 0.147
180
PNC127 Pancreatic Adenosquamous Carcinoma 34 0.147
181
P PNB001 Pineoblastoma 49 0.147
182
CNT019 Central Neurocytoma 46 0.147
183
CHL123 Chlamydia 58 0.147
184
PNC129 Pancreatic Adenocarcinoma 65 0.147
185
LYS002 Lysosomal Storage Disease 51 0.147
186
OST160 Osteoid Osteoma 37 0.147
187
VSC003 Visceral Leishmaniasis 54 0.147
188
CLF001 Cleft Lip 54 0.147
189
BBS001 Babesiosis 49 0.147
190
PPL013 Papillary Ependymoma 29 0.147
191
PNL014 Pineal Gland Cancer 40 0.147
192
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 0.147
193
MCP033 Mucopolysaccharidoses 44 0.147
194
LSH001 Leishmaniasis 63 0.147
195
P ART022 Arthritis 70 0.147
196
47X002 47,xyy 48 0.147
197
PNC056 Pineocytoma 44 0.147
198
CTN007 Cutaneous Leishmaniasis 61 0.147
199
ACT114 Acute Myeloblastic Leukemia Without Maturation 26 0.147
200
CLF056 Cleft Lip with or Without Cleft Palate 43 0.147
201
ANG050 Angiocentric Glioma 27 0.147
202
CLF004 Cleft Lip/palate 57 0.147
203
PPL050 Papillary Tumor of the Pineal Region 31 0.147
204
c MNS014 Monosomy 22 34 0.147
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