Search results for mos

327 hits were found for mos

# Family MCID Name MIFTS Score
1
SRC014 Sarcoma 65 5.421
2
P CFF008 Coffin-Siris Syndrome 1 63 3.748
3
SPN030 Spondyloepimetaphyseal Dysplasia, Missouri Type 43 3.067
4
PRT009 Parotid Gland Cancer 36 2.650
5
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.145
6
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.145
7
HRW001 Hair Whorl 36 0.141
8
P LKM002 Leukemia 68 0.130
9
IRN002 Iron Metabolism Disease 57 0.125
10
SPN035 Spindle Cell Sarcoma 53 0.113
11
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.113
12
P MYL006 Myeloid Leukemia 60 0.106
13
MNK001 Menkes Disease 64 0.099
14
P TRT010 Teratoma 52 0.099
15
47X002 47,xyy 49 0.099
16
P ALZ034 Alzheimer Disease 88 0.092
17
c LKM061 Leukemia, Acute Myeloid 84 0.092
18
P LVR013 Liver Disease 68 0.092
19
P TRN020 Turner Syndrome 67 0.092
20
P ADN016 Adenocarcinoma 64 0.092
21
48X005 48,xyyy 39 0.092
22
P RSP003 Respiratory Failure 74 0.084
23
DFC004 Deficiency Anemia 70 0.084
24
ART016 Aortic Aneurysm 69 0.084
25
P DMN002 Dementia 66 0.084
26
KHL003 Kohlschutter-Tonz Syndrome 65 0.084
27
P VSC007 Vascular Disease 63 0.084
28
c FNC043 Fanconi Anemia, Complementation Group E 62 0.084
29
ALL026 Allergic Hypersensitivity Disease 62 0.084
30
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.084
31
VSL002 Visual Epilepsy 59 0.084
32
ANR040 Aneurysm 59 0.084
33
P ALC033 Alcohol Use Disorder 58 0.084
34
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.084
35
P SZR006 Seizure Disorder 56 0.084
36
PNG002 Pain Agnosia 51 0.084
37
P GND004 Gonadal Dysgenesis 48 0.084
38
PRT112 Portal Hypertension, Noncirrhotic 31 0.084
39
P LYM118 Lymphoma 68 0.075
40
IRN001 Iron Deficiency Anemia 59 0.075
41
ADN018 Adenoma 59 0.075
42
c ACT073 Acute Leukemia 58 0.075
43
P SPP010 Suppressor of Tumorigenicity 3 51 0.075
44
CHR178 Chromosomal Triplication 35 0.075
45
c PLM128 Pulmonary Hypertension, Primary, 2 29 0.075
46
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.075
47
P BRS047 Breast Cancer 97 0.065
48
c SYS001 Systemic Lupus Erythematosus 86 0.065
49
P BLD134 Bladder Cancer 79 0.065
50
DWN001 Down Syndrome 70 0.065
51
DRM006 Dermatitis 61 0.065
52
FBR047 Fibromyalgia 58 0.065
53
PLS011 Plasmacytoma 56 0.065
54
P DRR001 Diarrhea 55 0.065
55
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.065
56
DNT012 Dental Caries 53 0.065
57
BNR002 Bone Resorption Disease 48 0.065
58
HLX001 Helix Syndrome 47 0.065
59
KRT002 Keratomalacia 47 0.065
60
TRT001 Teratocarcinoma 45 0.065
61
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.065
62
BCK006 Back Pain 42 0.065
63
P CLR023 Colorectal Cancer 99 0.053
64
P LNG032 Lung Cancer 98 0.053
65
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.053
66
P OST002 Osteoporosis 74 0.053
67
SVR004 Severe Combined Immunodeficiency 73 0.053
68
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.053
69
P RTN024 Retinoblastoma 73 0.053
70
P GRF003 Graft-Versus-Host Disease 72 0.053
71
P PHC003 Pheochromocytoma 71 0.053
72
MYL005 Myelofibrosis 70 0.053
73
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.053
74
P MLN008 Melanoma 69 0.053
75
P LKM062 Leukemia, Acute Lymphoblastic 69 0.053
76
OST159 Osteogenic Sarcoma 66 0.053
77
TTN003 Tetanus 65 0.053
78
PRT037 Pertussis 65 0.053
79
c DBT099 Diabetes Mellitus, Type I 65 0.053
80
PLM031 Poliomyelitis 64 0.053
81
P CRN300 Coronary Heart Disease 1 63 0.053
82
NTR005 Nutritional Deficiency Disease 62 0.053
83
DPH001 Diphtheria 60 0.053
84
CHR288 Chronic Recurrent Multifocal Osteomyelitis 60 0.053
85
ACQ007 Acquired Immunodeficiency Syndrome 60 0.053
86
OCC006 Occipital Horn Syndrome 60 0.053
87
P GLL022 Guillain-Barre Syndrome 59 0.053
88
GST045 Gastroenteritis 59 0.053
89
BRN056 Bronchopulmonary Dysplasia 57 0.053
90
THY122 Thyroid Gland Cancer 57 0.053
91
P MLT074 Multiple Endocrine Neoplasia 56 0.053
92
TRN018 Transitional Cell Carcinoma 56 0.053
93
EMB004 Embryonal Carcinoma 56 0.053
94
P RST001 Restless Legs Syndrome 54 0.053
95
c FML008 Familial Retinoblastoma 53 0.053
96
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.053
97
P RCT021 Rectum Cancer 52 0.053
98
TRM010 Traumatic Brain Injury 51 0.053
99
BRN071 Brain Injury 49 0.053
100
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.053
101
DGN001 Degenerative Disc Disease 48 0.053
102
P OVR046 Ovarian Cyst 47 0.053
103
BLC012 Bile Acid Malabsorption, Primary 45 0.053
104
c PRM038 Primary Agammaglobulinemia 44 0.053
105
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.053
106
P RNG032 Ring Chromosome 42 0.053
107
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 20 0.053
108
c PHT011 Photoparoxysmal Response 3 14 0.053
109
P HPT023 Hepatocellular Carcinoma 100 0.038
110
ESP021 Esophageal Cancer 90 0.038
111
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.038
112
P OVR042 Ovarian Cancer 88 0.038
113
c HYP595 Hypertension, Essential 84 0.038
114
P GST053 Gastric Cancer 83 0.038
115
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.038
116
P RHM011 Rheumatoid Arthritis 80 0.038
117
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.038
118
c NRF023 Neurofibromatosis, Type Ii 80 0.038
119
INS024 Insulin-Like Growth Factor I 79 0.038
120
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.038
121
P MDL005 Medulloblastoma 77 0.038
122
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.038
123
KPS004 Kaposi Sarcoma 75 0.038
124
END057 Endometrial Cancer 74 0.038
125
c HMC039 Hemochromatosis, Type 1 74 0.038
126
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.038
127
MSC157 Muscular Dystrophy, Duchenne Type 72 0.038
128
P KDN018 Kidney Disease 72 0.038
129
P MLT020 Multiple Sclerosis 72 0.038
130
c HPT073 Hepatitis C Virus 72 0.038
131
P NRB001 Neuroblastoma 72 0.038
132
c LKM063 Leukemia, Chronic Myeloid 72 0.038
133
c EXD008 Exudative Vitreoretinopathy 1 71 0.038
134
MYL009 Myelodysplastic Syndrome 70 0.038
135
c CHR684 Chronic Kidney Disease 70 0.038
136
P MYP004 Myopathy 70 0.038
137
CRB037 Cerebral Palsy 69 0.038
138
ODN023 Odontochondrodysplasia 68 0.038
139
P PNM007 Pneumonia 68 0.038
140
CHL065 Cholangiocarcinoma 68 0.038
141
SKN019 Skin Melanoma 68 0.038
142
P MYS003 Myasthenia Gravis 68 0.038
143
P INF038 Influenza 68 0.038
144
P ESS003 Essential Thrombocythemia 68 0.038
145
RCK004 Rickets 68 0.038
146
P THR014 Thrombocytopenia 67 0.038
147
GST092 Gastroesophageal Reflux 67 0.038
148
BRK010 Burkitt Lymphoma 67 0.038
149
THY111 Thyroid Carcinoma, Familial Medullary 67 0.038
150
c RHB024 Rhabdomyosarcoma 2 67 0.038
151
ALC007 Alcohol Dependence 66 0.038
152
P MSC005 Muscular Dystrophy 66 0.038
153
P SKN015 Skin Carcinoma 66 0.038
154
P HYD006 Hydrocephalus 66 0.038
155
P MNN013 Meningitis 66 0.038
156
P DRM053 Dermatitis, Atopic 66 0.038
157
P BRD002 Bardet-Biedl Syndrome 66 0.038
158
P LPS002 Liposarcoma 65 0.038
159
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 0.038
160
P HRP006 Herpes Simplex 65 0.038
161
ATH013 Atherosclerosis Susceptibility 65 0.038
162
P THY023 Thymoma 65 0.038
163
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.038
164
PRT036 Peritonitis 64 0.038
165
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.038
166
ANG020 Angiosarcoma 64 0.038
167
CLR108 Colorectal Adenoma 64 0.038
168
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.038
169
c PRC016 Pre-Eclampsia 63 0.038
170
ACT119 Acute Promyelocytic Leukemia 63 0.038
171
P LMY004 Leiomyosarcoma 63 0.038
172
c ALP101 Alpha-Thalassemia 62 0.038
173
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.038
174
P PSR002 Psoriasis 62 0.038
175
LPP008 Lipoprotein Quantitative Trait Locus 62 0.038
176
P HYP750 Hypertriglyceridemia, Familial 62 0.038
177
P ESP024 Esophagitis 62 0.038
178
ATM095 Autoimmune Disease 62 0.038
179
TXC005 Toxic Shock Syndrome 62 0.038
180
BLD131 Bladder Urothelial Carcinoma 62 0.038
181
MCK005 Mckusick-Kaufman Syndrome 61 0.038
182
HYP066 Hyperglycemia 61 0.038
183
P ENC018 Encephalopathy 61 0.038
184
YLL002 Yellow Fever 61 0.038
185
GST033 Gestational Diabetes 61 0.038
186
RTN017 Retinal Detachment 61 0.038
187
SPN186 Spinal Cord Injury 60 0.038
188
P NPH012 Nephrotic Syndrome 60 0.038
189
STT001 Status Epilepticus 60 0.038
190
P THL005 Thalassemia 60 0.038
191
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.038
192
P MCR010 Microcephaly 59 0.038
193
CHL014 Cholera 59 0.038
194
THY029 Thyroid Carcinoma 59 0.038
195
IGR001 Ige Responsiveness, Atopic 59 0.038
196
MTC097 Mitochondrial Complex Iv Deficiency 59 0.038
197
P LYM033 Lymphoproliferative Syndrome 59 0.038
198
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.038
199
P ANP001 Anaplastic Large Cell Lymphoma 58 0.038
200
ISC004 Ischemia 58 0.038
201
P BCL017 B-Cell Lymphoma 58 0.038
202
EYD002 Eye Disease 58 0.038
203
CNS004 Constipation 58 0.038
204
EXT034 Extrinsic Allergic Alveolitis 58 0.038
205
P GLM007 Glomerulonephritis 57 0.038
206
P FCL005 Focal Segmental Glomerulosclerosis 57 0.038
207
P CRD246 Cardiovascular System Disease 57 0.038
208
HYP266 Hypoxia 57 0.038
209
P BPL003 Bipolar Disorder 56 0.038
210
CMR002 Coumarin Resistance 56 0.038
211
P MTC069 Mitochondrial Disorders 56 0.038
212
P NRP001 Neuropathy 56 0.038
213
SFT003 Soft Tissue Sarcoma 56 0.038
214
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.038
215
ORL005 Oral Candidiasis 56 0.038
216
P PLY019 Polyneuropathy 56 0.038
217
AGN016 Aging 56 0.038
218
FND002 Fundus Dystrophy 55 0.038
219
MMB001 Membranoproliferative Glomerulonephritis 55 0.038
220
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.038
221
PRP030 Purpura 54 0.038
222
MNN032 Meningococcal Meningitis 54 0.038
223
P ALP008 Alopecia 54 0.038
224
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.038
225
AMN001 Amenorrhea 54 0.038
226
P LTR001 Lateral Sclerosis 54 0.038
227
WST005 West Nile Virus 54 0.038
228
P BRC006 Brachydactyly 53 0.038
229
PST046 Post-Transplant Lymphoproliferative Disease 53 0.038
230
c EXS019 Exostoses, Multiple, Type I 53 0.038
231
P MNC007 Monocytic Leukemia 53 0.038
232
OCL006 Ocular Hypertension 53 0.038
233
P RTN022 Retinal Vein Occlusion 53 0.038
234
c PSR017 Psoriasis 2 53 0.038
235
PST011 Pustulosis of Palm and Sole 52 0.038
236
ART140 Arteries, Anomalies of 52 0.038
237
P MSC003 Muscular Atrophy 52 0.038
238
c THY107 Thymoma, Familial 52 0.038
239
c PSR023 Psoriasis 1 52 0.038
240
PPT001 Peptic Esophagitis 52 0.038
241
c INH030 Inherited Retinal Disorder 51 0.038
242
INT079 Intrahepatic Cholangiocarcinoma 51 0.038
243
SPN019 Spondylolisthesis 51 0.038
244
P HYP040 Hypospadias 51 0.038
245
P OVR082 Overgrowth Syndrome 50 0.038
246
PST021 Postpartum Depression 50 0.038
247
P MTR003 Mitral Valve Stenosis 50 0.038
248
NPH018 Nephrogenic Systemic Fibrosis 50 0.038
249
THY125 Thyroid Gland Medullary Carcinoma 50 0.038
250
P TMP001 Temporal Lobe Epilepsy 50 0.038
251
P OBS001 Obstructive Jaundice 50 0.038
252
c LRG001 Large Cell Carcinoma 50 0.038
253
HYP080 Hypogonadism 50 0.038
254
ENT004 Enthesopathy 49 0.038
255
c BRD018 Bardet-Biedl Syndrome 6 49 0.038
256
P OPN001 Open-Angle Glaucoma 49 0.038
257
MYL003 Myeloid Sarcoma 49 0.038
258
VCC001 Vaccinia 49 0.038
259
IGG001 Iga Glomerulonephritis 48 0.038
260
MLT152 Multiple Self-Healing Squamous Epithelioma 47 0.038
261
c PSR032 Psoriasis 11 47 0.038
262
TTR011 Tetraploidy 47 0.038
263
c CNG216 Congenital Hydrocephalus 47 0.038
264
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.038
265
PLC003 Placental Site Trophoblastic Tumor 47 0.038
266
CHR074 Choriocarcinoma 47 0.038
267
NSS002 Neisseria Meningitidis Infection 47 0.038
268
LYM019 Lymphosarcoma 46 0.038
269
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.038
270
c 46X082 46,xy Sex Reversal 46 0.038
272
ORC001 Orchitis 46 0.038
273
MNN020 Meningococcal Infection 46 0.038
274
P BNG032 Benign Mesothelioma 46 0.038
275
ADR040 Adrenal Gland Pheochromocytoma 46 0.038
276
HDN002 Head Injury 46 0.038
277
P HRD001 Hereditary Multiple Exostoses 46 0.038
278
OBS037 Obesity-Hypoventilation Syndrome 46 0.038
279
SYN036 Syncope 45 0.038
280
LYM008 Lymphangiosarcoma 45 0.038
282
ATN004 Autonomic Neuropathy 45 0.038
283
P OST028 Osteochondroma 45 0.038
284
c PCH010 Pachyonychia Congenita 3 44 0.038
285
P MTC004 Mitochondrial Encephalomyopathy 44 0.038
286
P PRL003 Proliferative Glomerulonephritis 44 0.038
287
SMN007 Seminoma 43 0.038
288
DNT001 Dental Fluorosis 43 0.038
289
CYT002 Cytokine Deficiency 42 0.038
290
c PSR028 Psoriasis 7 42 0.038
291
c MLG064 Malignant Ependymoma 41 0.038
292
GST020 Gastric Antral Vascular Ectasia 41 0.038
293
MTL005 Metal Allergy 41 0.038
294
c PSR018 Psoriasis 13 41 0.038
295
c MJR024 Major Affective Disorder 9 41 0.038
296
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.038
297
c EXS020 Exostoses, Multiple, Type Ii 40 0.038
298
SKL017 Skeletal Dysplasias 40 0.038
299
PLY100 Polyploidy 40 0.038
300
c ACT004 Acute Diarrhea 39 0.038
301
P OTT001 Otitis Externa 39 0.038
302
c HRD104 Hereditary Multiple Osteochondromas 39 0.038
303
c MJR022 Major Affective Disorder 8 38 0.038
304
TRP005 Trophoblastic Neoplasm 38 0.038
305
c AMY062 Amyotrophic Lateral Sclerosis 12 37 0.038
306
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 36 0.038
307
PRN029 Parainfluenza Virus Type 3 36 0.038
308
P MTP005 Metaphyseal Anadysplasia 35 0.038
309
MTH047 Methanol Poisoning 34 0.038
310
c LKM005 Leukemia, T-Cell, Chronic 34 0.038
311
NND010 Nondisjunction 34 0.038
312
GRM010 Germ Cells Tumors 34 0.038
313
RHM034 Rahman Syndrome 34 0.038
314
c RST012 Restless Legs Syndrome 1 34 0.038
315
NNN007 Non-Involuting Congenital Hemangioma 33 0.038
316
HND015 Hand Skill, Relative 33 0.038
317
CHN003 Chondroblastic Osteosarcoma 29 0.038
318
THY006 Thymus Lymphoma 26 0.038
319
MTH071 Methane Production 26 0.038
320
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.038
321
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.038
322
LSS039 Lissencephaly 6 with Microcephaly 23 0.038
323
TTR021 Tetrasomy 21 22 0.038
324
c RNG025 Ring Chromosome 9 20 0.038
325
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 0.038
326
P TLN014 Tl Antigen 19 0.038
327
OBN001 Ouabain Resistance 18 0.038
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