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Search results for nog

354 hits were found for nog

# Family MCID Name MIFTS Score
1
TRS002 Tarsal-Carpal Coalition Syndrome 42 54.147
2
P PRX021 Proximal Symphalangism 50 41.727
3
c MLT059 Multiple Synostoses Syndrome 1 32 40.960
4
c BRC052 Brachydactyly, Type B2 40 40.156
5
c SYM022 Symphalangism, Proximal, 1a 29 39.175
6
P MLT072 Multiple Synostoses Syndrome 44 37.114
7
STP011 Stapes Ankylosis with Broad Thumbs and Toes 31 34.152
8
ANK001 Ankylosis 51 20.661
9
P BRC006 Brachydactyly 51 18.452
10
SYN005 Synostosis 43 16.692
11
SVR004 Severe Combined Immunodeficiency 72 16.040
12
P OTS001 Otosclerosis 49 15.351
13
ESP020 Esophageal Atresia 60 14.535
14
FBR011 Fibrodysplasia Ossificans Progressiva 67 14.007
15
P PRS040 Prostate Cancer 95 13.300
16
NRL016 Neural Tube Defects 81 13.001
17
c BRC051 Brachydactyly, Type B1 50 12.372
18
CLF027 Cleft Palate, Isolated 64 12.259
19
P OST002 Osteoporosis 76 12.133
20
P CRN037 Craniosynostosis 68 12.019
21
CHR619 Chromosome 2q35 Duplication Syndrome 64 11.795
22
P HLP001 Holoprosencephaly 69 11.436
23
P SCL048 Sclerosteosis 58 11.408
24
P BND020 Bone Disease 59 10.113
25
PFF001 Pfeiffer Syndrome 77 9.404
26
OSS012 Osseous Heteroplasia, Progressive 61 9.404
27
FRS019 Farsightedness 36 8.937
28
ABR009 Abruzzo-Erickson Syndrome 45 8.456
29
c BRC079 Brachydactyly, Type A2 50 7.358
30
c BRC078 Brachydactyly, Type A1 54 7.151
31
DPN005 Du Pan Syndrome 47 6.650
32
SYN031 Synovial Chondromatosis 41 6.650
33
c BRC080 Brachydactyly, Type A1, B 37 6.650
34
SGR001 Sugarman Brachydactyly 32 6.650
35
P RTN008 Retinitis Pigmentosa 80 6.650
36
SYN086 Synostoses, Tarsal, Carpal, and Digital 37 6.650
37
P JVN014 Juvenile Polyposis Syndrome 64 6.650
38
CHR569 Chromosomal Duplication Syndrome 21 6.650
39
P ORF002 Orofacial Cleft 43 6.650
40
HYL004 Hyaline Fibromatosis Syndrome 67 6.650
41
HMR015 Humeroradial Synostosis 36 6.650
42
c DMN023 Diamond-Blackfan Anemia 1 66 6.650
43
c BRC075 Brachydactyly, Type A1, C 34 6.650
44
DYS018 Dysostosis 44 6.650
45
GST026 Gastric Fundus Cancer 32 6.650
46
P BND014 Bone Development Disease 33 6.650
47
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 50 6.650
48
GRM001 Germ Cell and Embryonal Cancer 25 6.650
49
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 5.984
50
P GRF003 Graft-Versus-Host Disease 71 5.603
51
CMB007 Combined Immunodeficiency 57 5.022
52
c BRN108 Branchiootic Syndrome 1 62 4.109
53
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 3.661
54
c LKM005 Leukemia, T-Cell, Chronic 34 3.661
55
P ADL017 Adult T-Cell Leukemia 56 3.620
56
c HMN021 Human T-Cell Leukemia Virus Type 1 47 3.520
57
P HRP006 Herpes Simplex 65 3.355
58
MYL069 Myeloma, Multiple 77 2.995
59
GLB002 Glioblastoma 67 2.910
60
P PNC035 Pancreatic Cancer 86 2.860
61
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 54 2.855
62
P SNS001 Sensorineural Hearing Loss 59 2.810
63
P BRS047 Breast Cancer 98 2.728
64
HMN044 Human Immunodeficiency Virus Type 1 78 2.555
65
CLF001 Cleft Lip 53 2.489
66
SPP007 Suppression Amblyopia 38 2.489
67
AMB002 Amblyopia 50 2.489
68
P TRT010 Teratoma 51 2.489
69
c HPT016 Hepatitis B 62 2.489
70
c ACT134 Acute Liver Failure 59 2.373
71
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 2.350
72
P RHB003 Rhabdomyosarcoma 66 2.350
73
CLF056 Cleft Lip with or Without Cleft Palate 42 2.350
74
c PRX100 Proximal Symphalangism 2 5 2.287
75
P MLN008 Melanoma 76 2.276
76
P STR020 Strabismus 56 2.199
77
MCH006 Mechanical Strabismus 40 2.199
78
P ALP008 Alopecia 54 2.118
79
P CTR002 Cataract 60 2.118
80
P RTN018 Retinal Disease 53 2.118
81
P OST001 Osteopetrosis 71 2.118
82
P VTR007 Vitreoretinopathy 46 2.032
83
RTN017 Retinal Detachment 60 2.032
84
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 61 2.032
85
c LKM063 Leukemia, Chronic Myeloid 71 2.032
86
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 2.032
87
ADN018 Adenoma 59 2.032
88
P OVR082 Overgrowth Syndrome 49 1.990
89
MYL005 Myelofibrosis 71 1.940
90
P LVR013 Liver Disease 69 1.940
91
P SKN015 Skin Carcinoma 71 1.940
92
c SYM019 Symphalangism, Proximal, 1b 25 1.940
93
c SPN225 Spondyloarthropathy 1 70 1.874
94
P NRB001 Neuroblastoma 66 1.874
95
SPN051 Spondylitis 51 1.874
96
INF009 Inflammatory Spondylopathy 30 1.874
97
P LKM002 Leukemia 67 1.874
98
P MYS005 Myositis 56 1.872
99
OST017 Osteomyelitis 63 1.872
100
P HYP083 Hypopituitarism 52 1.872
101
P ENC004 Encephalitis 61 1.872
102
c EXD008 Exudative Vitreoretinopathy 1 71 1.842
103
SFT003 Soft Tissue Sarcoma 57 1.842
104
SPL018 Splenomegaly 49 1.842
105
PLY001 Polycythemia Vera 69 1.735
106
P PLY018 Polycythemia 56 1.735
107
P ESS003 Essential Thrombocythemia 69 1.735
108
PRM013 Premature Menopause 58 1.735
109
THY006 Thymus Lymphoma 27 1.661
110
P HPT021 Hepatitis 69 1.661
111
TRS030 Tarsal Coalition 25 1.617
112
c LKM061 Leukemia, Acute Myeloid 83 1.617
113
P LKM062 Leukemia, Acute Lymphoblastic 69 1.584
114
P SPN237 Spina Bifida Aperta 19 1.483
115
SPS019 Spastic Paraparesis 38 1.483
116
AGM019 Agammaglobulinemia, X-Linked 72 1.483
117
P LYM118 Lymphoma 67 1.483
118
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.483
119
MYL057 Myelopathy, Htlv-1-Associated 38 1.483
120
HPT067 Hepatocellular Adenoma 43 1.483
121
P MYL006 Myeloid Leukemia 61 1.483
122
MCR173 Microform Holoprosencephaly 44 1.483
123
FDL002 Food Allergy 47 1.483
124
P LCT001 Lactic Acidosis 51 1.483
125
MLK006 Milk Allergy 47 1.483
126
BLR001 Biliary Atresia 55 1.483
127
P AGM001 Agammaglobulinemia 68 1.483
128
CWM001 Cow Milk Allergy 36 1.483
129
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.483
130
TRP002 Tropical Spastic Paraparesis 49 1.483
131
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 38 1.483
132
P RCT021 Rectum Cancer 54 1.416
133
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.376
134
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.325
135
BRK010 Burkitt Lymphoma 66 1.324
136
ANX010 Anxiety 70 1.227
137
P SLP006 Sleep Apnea 69 1.227
138
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.227
139
P PRP019 Peripheral Nervous System Disease 58 1.227
140
P LMY004 Leiomyosarcoma 62 1.227
141
c CNG596 Congenital Ectropion 16 1.120
142
CNG335 Congenital Ectropion Uveae 12 1.120
143
WBR001 Weber Syndrome 38 1.120
144
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 1.120
145
BCL014 B-Cell Growth Factor 33 1.120
146
AGN016 Aging 54 1.120
147
P PHC003 Pheochromocytoma 69 1.120
148
STR039 Sturge-Weber Syndrome 61 1.120
149
c OTS005 Otosclerosis 1 25 1.120
150
c OTS007 Otosclerosis 3 18 1.120
151
P ATR011 Atrial Fibrillation 66 1.120
152
c PRM032 Primary Congenital Glaucoma 41 1.120
153
c OTS006 Otosclerosis 2 16 1.120
154
INT323 Intraocular Pressure Quantitative Trait Locus 64 1.120
155
c OTS009 Otosclerosis 5 12 1.120
156
ADR040 Adrenal Gland Pheochromocytoma 46 1.120
157
P RBL001 Rubella 58 1.120
158
P THR014 Thrombocytopenia 66 1.120
159
SPN035 Spindle Cell Sarcoma 54 1.120
160
TXC005 Toxic Shock Syndrome 62 1.120
161
P ADN016 Adenocarcinoma 63 1.120
162
SRC014 Sarcoma 65 1.120
163
CRB039 Cerebrovascular Disease 66 1.120
164
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 1.120
165
ISC004 Ischemia 61 1.120
166
P TMP001 Temporal Lobe Epilepsy 49 1.120
167
P ECT005 Ectropion 41 1.120
168
CNG124 Congenital Rubella 43 1.120
169
P PLY006 Polydactyly 59 1.116
170
THS001 Thai Symphalangism Syndrome 12 1.116
171
LNG105 Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome 35 1.116
172
P PTS002 Ptosis 52 1.116
173
STR067 Stroke, Ischemic 80 1.002
174
P RHM011 Rheumatoid Arthritis 82 1.002
175
P MLN069 Melanoma, Uveal 61 1.002
176
P LKM071 Leukemia, Chronic Lymphocytic 75 1.002
177
FCT001 Factor Viii Deficiency 60 1.002
178
IMM167 Immune Deficiency Disease 78 1.002
179
c OTS010 Otosclerosis 7 15 1.002
180
c HMP029 Hemophilia a 68 1.002
181
P ART022 Arthritis 71 1.002
182
HPT085 Hepatitis, Fulminant Viral 33 1.002
183
GTR002 Goiter 53 1.002
184
TCL001 T-Cell Adult Acute Lymphocytic Leukemia 43 1.002
185
EMB004 Embryonal Carcinoma 56 1.002
186
P HMP007 Hemophilia 52 1.002
187
c PRX099 Proximal Symphalangism 1 5 0.871
188
LYM133 Lymphoma, Hodgkin, Classic 74 0.867
189
P NSP012 Nasopharyngeal Carcinoma 61 0.867
190
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.867
191
PLY150 Polykaryocytosis Inducer 29 0.867
192
INT029 Interleukin-7 Receptor Alpha Deficiency 28 0.867
193
LMY014 Leiomyoma, Uterine 56 0.867
195
c NPH055 Nephrotic Syndrome, Type 1 52 0.867
196
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.867
197
c HYP864 Hypoparathyroidism, Familial Isolated, 1 30 0.867
198
P SCL018 Scoliosis 57 0.867
199
LMY002 Leiomyoma 51 0.867
200
OCL006 Ocular Hypertension 53 0.867
201
P PRS038 Personality Disorder 65 0.867
202
THY022 Thymic Carcinoma 57 0.867
203
P PLM036 Pulmonary Fibrosis 66 0.867
204
P RTN016 Retinal Degeneration 52 0.867
205
LNG099 Lung Disease 62 0.867
206
P PRD008 Periodontitis 64 0.867
207
RTN003 Retinal Ischemia 49 0.867
208
MST005 Mastitis 53 0.867
209
P MCR010 Microcephaly 60 0.867
210
ANT011 Antisocial Personality Disorder 47 0.867
211
LVR012 Liver Cirrhosis 63 0.867
212
PRM024 Primary Angle-Closure Glaucoma 39 0.867
213
HYP056 Hypoglycemia 65 0.867
215
P LNG032 Lung Cancer 98 0.708
216
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 0.708
217
ART140 Arteries, Anomalies of 53 0.708
218
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.708
219
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.708
220
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.708
221
CRV035 Cervical Cancer 73 0.708
222
c BRC081 Brachydactyly, Type C 48 0.708
223
c MST023 Mesothelioma, Malignant 56 0.708
224
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.708
225
P PLM037 Pulmonary Hypertension 72 0.708
227
FTL006 Fetal Alcohol Spectrum Disorder 43 0.708
228
DFF005 Diffuse Large B-Cell Lymphoma 54 0.708
229
LPP008 Lipoprotein Quantitative Trait Locus 65 0.708
230
P CTN015 Cutaneous T Cell Lymphoma 48 0.708
231
TRC097 Tracheomalacia 43 0.708
232
P LYM033 Lymphoproliferative Syndrome 59 0.708
233
BNR002 Bone Resorption Disease 47 0.708
234
P FTL001 Fetal Alcohol Syndrome 55 0.708
235
P CHN012 Chondrosarcoma 57 0.708
236
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.708
237
HSH003 Hashimoto Thyroiditis 60 0.708
238
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.708
239
c MLT166 Multiple Synostoses Syndrome 4 20 0.708
240
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.708
241
c PCH010 Pachyonychia Congenita 3 43 0.708
242
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.708
243
CHR381 Chromosome 17q23.1-Q23.2 Deletion Syndrome 34 0.708
244
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.708
245
SVR097 Severe Cutaneous Adverse Reaction 69 0.708
246
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.708
247
RDL040 Radioulnar Synostosis, Nonsyndromic 29 0.708
248
HRW001 Hair Whorl 35 0.708
249
c MLT060 Multiple Synostoses Syndrome 2 29 0.708
250
CHL065 Cholangiocarcinoma 58 0.708
251
ERY066 Erythema Multiforme Major 29 0.708
252
c ACT073 Acute Leukemia 58 0.708
253
P BCL017 B-Cell Lymphoma 59 0.708
254
SKN019 Skin Melanoma 71 0.708
255
P RDL002 Radioulnar Synostosis 47 0.708
256
MTH009 Mouth Disease 57 0.708
257
P THY032 Thyroiditis 57 0.708
258
MLG079 Malignant Pleural Mesothelioma 42 0.708
259
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.708
260
ERY003 Erythema Multiforme 56 0.708
261
PLC002 Plica Syndrome 35 0.708
262
OLG003 Oligohydramnios 51 0.708
263
MYL031 Myeloproliferative Neoplasm 66 0.708
264
P HYD006 Hydrocephalus 61 0.708
265
INT079 Intrahepatic Cholangiocarcinoma 51 0.708
266
PRP030 Purpura 54 0.708
267
SYN007 Synovitis 55 0.708
268
P BNG032 Benign Mesothelioma 53 0.708
269
NRN004 Neuroendocrine Tumor 59 0.708
270
c ACT135 Acute Graft Versus Host Disease 51 0.708
271
ACT200 Acute Monoblastic Leukemia 41 0.708
272
IDP033 Idiopathic Edema 41 0.708
273
P HYP265 Hypotonia 42 0.708
274
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 0.708
275
P MYC084 Mycobacterium Tuberculosis 1 68 0.615
276
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.615
277
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.615
278
TRC035 Tracheal Agenesis 30 0.573
279
CLF004 Cleft Lip/palate 57 0.501
280
SPN186 Spinal Cord Injury 61 0.501
281
P ALZ034 Alzheimer Disease 87 0.501
282
P BLD134 Bladder Cancer 79 0.501
283
RST023 Resting Heart Rate, Variation in 40 0.501
284
ANR007 Anorexia Nervosa 60 0.501
285
P DRM053 Dermatitis, Atopic 65 0.501
286
BRT054 Brittle Bone Disorder 74 0.501
287
END057 Endometrial Cancer 72 0.501
288
P OVR042 Ovarian Cancer 88 0.501
289
P ALG028 Alagille Syndrome 1 73 0.501
290
P MLT020 Multiple Sclerosis 79 0.501
291
PRN038 Prune Belly Syndrome 56 0.501
292
PRP080 Peripheral Artery Disease 54 0.501
293
PRP036 Peripheral T-Cell Lymphoma 53 0.501
294
P INF037 Inflammatory Bowel Disease 53 0.501
295
LMB062 Limb Ischemia 55 0.501
296
CLT003 Colitis 63 0.501
297
c RTN041 Retinitis Pigmentosa 11 42 0.501
298
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.501
299
SPN060 Spondylocarpotarsal Synostosis Syndrome 49 0.501
300
c CHR320 Chiari Malformation Type I 46 0.501
301
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.501
302
P GST053 Gastric Cancer 83 0.501
303
SMT018 Smith-Mccort Dysplasia 2 34 0.501
304
c OTS012 Otosclerosis 10 16 0.501
305
c HPT073 Hepatitis C Virus 71 0.501
306
c OTS011 Otosclerosis 8 15 0.501
307
ACT119 Acute Promyelocytic Leukemia 62 0.501
308
DWN001 Down Syndrome 70 0.501
309
P SRC025 Sarcoidosis 1 71 0.501
310
ESP021 Esophageal Cancer 83 0.501
311
P HPT023 Hepatocellular Carcinoma 96 0.501
312
SYM012 Symphalangism, Distal, with Microdontia, Dental Pulp Stones, and Narrowed Zygomatic Arch 14 0.501
313
GST019 Gastrointestinal Stromal Tumor 78 0.501
314
THY029 Thyroid Carcinoma 51 0.501
315
P HYP730 Hypogonadotropic Hypogonadism 53 0.501
316
TRM010 Traumatic Brain Injury 51 0.501
317
URM002 Uremia 47 0.501
318
ALL006 Allergic Asthma 56 0.501
319
P HYP098 Hypereosinophilic Syndrome 66 0.501
320
ORF053 Orofacial Clefting Syndrome 31 0.501
321
WHT017 Wheat Allergy 31 0.501
322
INT002 Intermittent Claudication 61 0.501
323
c HPT001 Hepatitis C 62 0.501
324
ACQ007 Acquired Immunodeficiency Syndrome 59 0.501
325
OST012 Osteoarthritis 77 0.501
326
P MNC007 Monocytic Leukemia 47 0.501
327
CRB004 Cerebral Artery Occlusion 45 0.501
328
P LNG064 Lung Cancer Susceptibility 3 70 0.501
329
SCR003 Secretory Diarrhea 35 0.501
330
P KLP003 Klippel-Feil Syndrome 47 0.501
331
ALL029 Allergic Disease 59 0.501
332
P MLN007 Male Infertility 56 0.501
333
P DDN001 Duodenal Ulcer 53 0.501
334
P HYP040 Hypospadias 51 0.501
335
THY020 Thyroid Hyalinizing Trabecular Adenoma 20 0.501
336
P END047 Endophthalmitis 53 0.501
337
P INF032 Infertility 57 0.501
338
CRT015 Carotid Artery Occlusion 45 0.501
339
DRM006 Dermatitis 62 0.501
340
GNT004 Gnathomiasis 29 0.501
341
HYP080 Hypogonadism 50 0.501
342
SQM006 Squamous Cell Carcinoma 60 0.501
343
ORL011 Oral Cancer 60 0.501
344
P PRC019 Precocious Puberty 47 0.501
345
BRN071 Brain Injury 50 0.501
346
HYP266 Hypoxia 57 0.501
347
P CHR342 Chiari Malformation 41 0.501
348
CHR178 Chromosomal Triplication 34 0.501
349
EXN003 Exencephaly 30 0.501
350
GNT023 Gnathostoma Infection 19 0.501
351
GLM045 Glioma 63 0.501
352
ETN001 Eating Disorder 59 0.501
353
HPT070 Hepatosplenic T-Cell Lymphoma 36 0.430
354
CHR020 Chronic Interstitial Cystitis 36 0.430
The MalaCards human disease database index: 1-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
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