Search results for B2

781 hits were found for B2

# Family MCID Name MIFTS Score
1
c BRC052 Brachydactyly, Type B2 41 7.579
2
c MSC044 Muscular Dystrophy-Dystroglycanopathy , Type B, 2 30 4.149
3
c CHR651 Charcot-Marie-Tooth Disease, Axonal, Type 2b2 39 3.376
4
RBF001 Riboflavin Deficiency 49 2.535
5
CRT005 Cortical Thymoma 24 2.387
6
P CLR023 Colorectal Cancer 99 0.123
7
BRN004 Brain Edema 56 0.121
8
c MCR113 Microvascular Complications of Diabetes 3 52 0.115
9
c MCR120 Microvascular Complications of Diabetes 7 47 0.115
10
c MCR130 Microvascular Complications of Diabetes 6 41 0.115
11
c MCR133 Microvascular Complications of Diabetes 4 41 0.115
12
c PRC016 Pre-Eclampsia 63 0.109
13
P MYC008 Myocarditis 59 0.109
14
PRT037 Pertussis 65 0.106
15
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.100
16
ISC004 Ischemia 58 0.100
17
c HYP595 Hypertension, Essential 84 0.093
18
P LVR013 Liver Disease 68 0.093
19
HLX001 Helix Syndrome 47 0.093
20
P ANG015 Angioedema 57 0.089
21
P HPT023 Hepatocellular Carcinoma 100 0.085
22
P ADN016 Adenocarcinoma 64 0.085
23
P BRS047 Breast Cancer 97 0.081
24
OST012 Osteoarthritis 78 0.077
25
P KDN018 Kidney Disease 72 0.077
26
P GLM045 Glioma 63 0.077
27
c ACT068 Acute Cystitis 63 0.077
28
P RHN004 Rhinitis 57 0.077
29
TRM010 Traumatic Brain Injury 51 0.077
30
BRN071 Brain Injury 49 0.077
31
P PRS040 Prostate Cancer 97 0.073
32
P BLD134 Bladder Cancer 79 0.073
33
c HYP836 Hypercholesterolemia, Familial, 1 73 0.073
34
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.073
35
CRB039 Cerebrovascular Disease 67 0.073
36
P PLM037 Pulmonary Hypertension 67 0.073
37
ANG054 Angina Pectoris 66 0.073
38
P THY023 Thymoma 65 0.073
39
P VSC007 Vascular Disease 63 0.073
40
P PSR002 Psoriasis 62 0.073
41
LPP008 Lipoprotein Quantitative Trait Locus 62 0.073
42
ADN018 Adenoma 59 0.073
43
P INF037 Inflammatory Bowel Disease 54 0.073
44
PST011 Pustulosis of Palm and Sole 52 0.073
45
ART140 Arteries, Anomalies of 52 0.073
46
c THY107 Thymoma, Familial 52 0.073
47
P MNN013 Meningitis 66 0.068
48
TXC005 Toxic Shock Syndrome 62 0.068
49
HYP066 Hyperglycemia 61 0.068
50
P THL005 Thalassemia 60 0.068
51
MTH009 Mouth Disease 56 0.068
52
END086 End Stage Renal Disease 51 0.068
53
P ECL001 Eclampsia 50 0.068
54
GLL048 Glial Tumor 45 0.068
55
CRB004 Cerebral Artery Occlusion 45 0.068
56
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.068
57
CRV035 Cervical Cancer 76 0.063
58
CRH001 Crohn's Disease 74 0.063
59
P MYC007 Myocardial Infarction 70 0.063
60
ALL003 Allergic Rhinitis 67 0.063
61
c MGR028 Migraine with or Without Aura 1 67 0.063
62
ALL026 Allergic Hypersensitivity Disease 62 0.063
63
P TMP001 Temporal Lobe Epilepsy 50 0.063
64
RNL077 Renal Fibrosis 47 0.063
65
48X005 48,xyyy 39 0.063
66
P LNG032 Lung Cancer 98 0.058
67
STR067 Stroke, Ischemic 81 0.058
68
AST005 Asthma 76 0.058
69
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.058
70
P NRB001 Neuroblastoma 72 0.058
71
CNG034 Congestive Heart Failure 69 0.058
72
ATH013 Atherosclerosis Susceptibility 65 0.058
73
P CRN300 Coronary Heart Disease 1 63 0.058
74
SKN016 Skin Disease 63 0.058
75
P NPH012 Nephrotic Syndrome 60 0.058
76
c HRD002 Hereditary Angioedema 60 0.058
77
P INF032 Infertility 57 0.058
78
THR024 Thrombosis 57 0.058
79
P CRD246 Cardiovascular System Disease 57 0.058
80
P NRP001 Neuropathy 56 0.058
81
EMB004 Embryonal Carcinoma 56 0.058
82
INT007 Intermediate Coronary Syndrome 55 0.058
83
P ART021 Arteriosclerosis 54 0.058
84
P RCT021 Rectum Cancer 52 0.058
85
CLR109 Colorectal Adenocarcinoma 51 0.058
86
ASP003 Aseptic Meningitis 51 0.058
87
MNN009 Meningoencephalitis 49 0.058
88
BNR002 Bone Resorption Disease 48 0.058
89
URT010 Ureteral Obstruction 45 0.058
90
CYT002 Cytokine Deficiency 42 0.058
91
ESP021 Esophageal Cancer 90 0.051
92
c ATR087 Atrial Standstill 1 75 0.051
93
P PHC003 Pheochromocytoma 71 0.051
94
DFC004 Deficiency Anemia 70 0.051
95
c CHR684 Chronic Kidney Disease 70 0.051
96
ART016 Aortic Aneurysm 69 0.051
97
P CLC063 Celiac Disease 1 66 0.051
98
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.051
99
P HRP006 Herpes Simplex 65 0.051
100
PRT036 Peritonitis 64 0.051
101
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.051
102
CLR108 Colorectal Adenoma 64 0.051
103
P RHB003 Rhabdomyosarcoma 63 0.051
104
P NTR004 Neutropenia 63 0.051
105
ATM095 Autoimmune Disease 62 0.051
106
LVR012 Liver Cirrhosis 62 0.051
107
MSL001 Measles 62 0.051
108
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.051
109
FTT001 Fatty Liver Disease 61 0.051
110
P ENC004 Encephalitis 61 0.051
111
SPN186 Spinal Cord Injury 60 0.051
112
CHL014 Cholera 59 0.051
113
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.051
114
c ACT075 Acute Myocardial Infarction 57 0.051
115
ALL006 Allergic Asthma 56 0.051
116
BCT022 Bacterial Infectious Disease 56 0.051
117
P DRR001 Diarrhea 55 0.051
118
HMC014 Homocysteinemia 53 0.051
119
OCL069 Ocular Motor Apraxia 51 0.051
120
P LCT001 Lactic Acidosis 51 0.051
121
HND002 Hand, Foot and Mouth Disease 51 0.051
122
PLR008 Pleurisy 50 0.051
123
HPT014 Hepatorenal Syndrome 50 0.051
124
MTB004 Metabolic Acidosis 50 0.051
125
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.051
126
ADR040 Adrenal Gland Pheochromocytoma 46 0.051
127
c LKM005 Leukemia, T-Cell, Chronic 34 0.051
128
NNT021 Neonatal Meningitis 25 0.051
129
P ALZ034 Alzheimer Disease 88 0.045
130
c SYS001 Systemic Lupus Erythematosus 86 0.045
131
c DLT002 Dilated Cardiomyopathy 79 0.045
132
ULC004 Ulcerative Colitis 73 0.045
133
PRP027 Peripheral Vascular Disease 71 0.045
134
P SLP006 Sleep Apnea 69 0.045
135
P THR014 Thrombocytopenia 67 0.045
136
P HPT021 Hepatitis 67 0.045
137
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.045
138
c RHB024 Rhabdomyosarcoma 2 67 0.045
139
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.045
140
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.045
141
KRT019 Keratitis, Hereditary 65 0.045
142
P DBT009 Diabetes Mellitus 64 0.045
143
DPR016 Depression 63 0.045
144
c ALP101 Alpha-Thalassemia 62 0.045
145
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.045
146
NTR005 Nutritional Deficiency Disease 62 0.045
147
DRM006 Dermatitis 61 0.045
148
P ENC018 Encephalopathy 61 0.045
149
ALC006 Alcoholic Hepatitis 61 0.045
150
P PNC044 Pancreatitis 61 0.045
151
P LPS004 Lupus Erythematosus 61 0.045
152
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.045
153
LNG099 Lung Disease 60 0.045
154
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.045
155
c ACT071 Acute Kidney Failure 60 0.045
156
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.045
157
P SLP005 Sleep Disorder 59 0.045
158
PLM033 Pulmonary Embolism 59 0.045
159
P CYS018 Cystitis 59 0.045
160
IRN001 Iron Deficiency Anemia 59 0.045
161
IRN002 Iron Metabolism Disease 57 0.045
162
P EXN002 Exanthem 57 0.045
163
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.045
164
HYP266 Hypoxia 57 0.045
165
P PYL005 Pyelonephritis 56 0.045
166
HMG005 Hemoglobinopathy 56 0.045
167
FDB001 Foodborne Botulism 55 0.045
168
PRP030 Purpura 54 0.045
169
DBT010 Diabetic Neuropathy 54 0.045
170
IMP005 Impotence 52 0.045
171
STT002 Status Asthmaticus 50 0.045
172
47X002 47,xyy 49 0.045
173
INT078 Intracranial Thrombosis 49 0.045
174
P RNV001 Renovascular Hypertension 48 0.045
175
c ACT076 Acute Myocarditis 46 0.045
176
ACT003 Acute Kidney Tubular Necrosis 45 0.045
177
P CHR345 Chronic Pain 44 0.045
178
c PCH010 Pachyonychia Congenita 3 44 0.045
179
c PRM038 Primary Agammaglobulinemia 44 0.045
180
C1N001 C1 Inhibitor Deficiency 39 0.045
181
c BLD156 Bleeding Disorder, Platelet-Type, 14 32 0.045
182
PST092 Posttransplant Acute Limbic Encephalitis 29 0.045
183
CHL079 Children's Interstitial Lung Disease 26 0.045
184
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.036
185
NRL016 Neural Tube Defects 82 0.036
186
P PRK057 Parkinson Disease, Late-Onset 78 0.036
187
c TBR025 Tuberous Sclerosis 1 77 0.036
188
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.036
189
P RSP003 Respiratory Failure 74 0.036
190
END057 Endometrial Cancer 74 0.036
191
c BTT014 Beta-Thalassemia 74 0.036
192
c THR092 Thrombophilia Due to Thrombin Defect 73 0.036
193
P RTN024 Retinoblastoma 73 0.036
194
c HPT073 Hepatitis C Virus 72 0.036
195
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.036
196
HMN044 Human Immunodeficiency Virus Type 1 71 0.036
197
P SRC025 Sarcoidosis 1 70 0.036
198
DWN001 Down Syndrome 70 0.036
199
P OST001 Osteopetrosis 70 0.036
200
P MYP004 Myopathy 70 0.036
201
P TBR001 Tuberous Sclerosis 70 0.036
202
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.036
203
PLM001 Pulmonary Tuberculosis 69 0.036
204
P LYM118 Lymphoma 68 0.036
205
P MYC084 Mycobacterium Tuberculosis 1 68 0.036
206
P LKM002 Leukemia 68 0.036
207
P ESS003 Essential Thrombocythemia 68 0.036
208
RCK004 Rickets 68 0.036
209
CRP001 Carpal Tunnel Syndrome 67 0.036
210
OST159 Osteogenic Sarcoma 66 0.036
211
c FML021 Familial Hypercholesterolemia 66 0.036
212
P MSC005 Muscular Dystrophy 66 0.036
213
P SKN015 Skin Carcinoma 66 0.036
214
P ATR011 Atrial Fibrillation 66 0.036
215
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.036
216
P VNW001 Von Willebrand's Disease 65 0.036
217
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.036
218
c DBT099 Diabetes Mellitus, Type I 65 0.036
219
CLN015 Colon Adenocarcinoma 65 0.036
220
APN008 Apnea, Obstructive Sleep 64 0.036
221
GT001 Gout 64 0.036
222
OST017 Osteomyelitis 64 0.036
223
LSH001 Leishmaniasis 63 0.036
224
P END044 Endometriosis 63 0.036
225
LPD008 Lipid Metabolism Disorder 62 0.036
226
c HPT001 Hepatitis C 62 0.036
227
P HYP750 Hypertriglyceridemia, Familial 62 0.036
228
CHR619 Chromosome 2q35 Duplication Syndrome 62 0.036
229
BRS099 Breast Ductal Carcinoma 62 0.036
230
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 61 0.036
231
c PNS012 Paine Syndrome 61 0.036
232
P MYL006 Myeloid Leukemia 60 0.036
233
c ACT027 Acute Pancreatitis 60 0.036
234
P CTR002 Cataract 60 0.036
235
STT001 Status Epilepticus 60 0.036
236
c HPT016 Hepatitis B 59 0.036
237
VSL002 Visual Epilepsy 59 0.036
238
GNG013 Gingivitis 59 0.036
239
GST045 Gastroenteritis 59 0.036
240
HLC007 Helicobacter Pylori Infection 59 0.036
241
PPT005 Peptic Ulcer Disease 59 0.036
242
FBR047 Fibromyalgia 58 0.036
243
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.036
244
P MTR012 Mitral Valve Disease 58 0.036
245
MNT002 Mental Depression 58 0.036
246
P GLM007 Glomerulonephritis 57 0.036
247
P ZLL001 Zellweger Syndrome 57 0.036
248
P HDC001 Headache 57 0.036
249
DSS009 Disseminated Intravascular Coagulation 57 0.036
250
CPR004 Coproporphyria, Hereditary 57 0.036
251
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.036
252
P PLY018 Polycythemia 56 0.036
253
P ADL017 Adult T-Cell Leukemia 56 0.036
254
P FBR017 Fibrosarcoma 56 0.036
255
LST001 Listeriosis 56 0.036
256
P MLT074 Multiple Endocrine Neoplasia 56 0.036
257
ERY051 Erythroleukemia, Familial 56 0.036
258
P SZR006 Seizure Disorder 56 0.036
259
CYS008 Cystic Echinococcosis 56 0.036
260
MCS002 Mucositis 56 0.036
261
P PLY019 Polyneuropathy 56 0.036
262
P GST044 Gastritis 56 0.036
263
LMB062 Limb Ischemia 55 0.036
264
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.036
265
P MYP006 Myopia 55 0.036
266
SYN007 Synovitis 54 0.036
267
P ALP008 Alopecia 54 0.036
268
PRC013 Pericarditis 54 0.036
269
PLM010 Pulmonary Edema 54 0.036
270
ECH003 Echinococcosis 53 0.036
271
P HML001 Hemolytic-Uremic Syndrome 53 0.036
272
GTR002 Goiter 53 0.036
273
NNT012 Neonatal Jaundice 53 0.036
274
c FML008 Familial Retinoblastoma 53 0.036
275
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.036
276
P DDN001 Duodenal Ulcer 52 0.036
277
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.036
278
P HMP007 Hemophilia 51 0.036
279
THR004 Thrombocytosis 51 0.036
280
ENT011 Enterocolitis 51 0.036
281
P LSS002 Lissencephaly 51 0.036
282
STM007 Stomatitis 50 0.036
283
PLC008 Placenta Disease 50 0.036
284
NTR046 Neutrophil Migration 50 0.036
285
RNL078 Renal Dysplasia 50 0.036
286
P MTC133 Mitochondrial Myopathy 49 0.036
287
c MTR002 Mitral Valve Insufficiency 48 0.036
288
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.036
289
HPR003 Heparin-Induced Thrombocytopenia 48 0.036
290
CRN017 Coronary Thrombosis 47 0.036
291
KRT002 Keratomalacia 47 0.036
292
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.036
293
CRD137 Cardiogenic Shock 47 0.036
294
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.036
295
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.036
296
HDN002 Head Injury 46 0.036
297
c MLG068 Malignant Glioma 46 0.036
298
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.036
299
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.036
300
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.036
301
P MTC004 Mitochondrial Encephalomyopathy 44 0.036
302
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.036
303
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.036
304
RFR003 Refractive Error 43 0.036
305
P CRN026 Corneal Edema 43 0.036
306
RNL025 Renal Hypoplasia 42 0.036
307
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.036
308
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.036
309
EPT021 Epithelial Recurrent Erosion Dystrophy 42 0.036
310
P KLZ004 Kala-Azar 1 41 0.036
311
ASP030 Aspirin Resistance 39 0.036
312
ALL014 Allergic Encephalomyelitis 38 0.036
313
EPL199 Epilepsy, Progressive Myoclonic, 4, with or Without Renal Failure 36 0.036
314
PLC002 Plica Syndrome 36 0.036
315
PYR009 Pyridoxine Deficiency Anemia 34 0.036
316
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.036
317
CMP040 Complement Component 4, Partial Deficiency of 33 0.036
318
c PRS136 Prostate Cancer, Hereditary, 6 33 0.036
319
c PRS130 Prostate Cancer, Hereditary, 8 32 0.036
320
PYR016 Pyridoxine Deficiency 30 0.036
321
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.036
322
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.036
323
IMM165 Immunoglobulin Switch Sequences 15 0.036
324
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.026
325
P OVR042 Ovarian Cancer 88 0.026
327
c LKM061 Leukemia, Acute Myeloid 84 0.026
328
P PNC035 Pancreatic Cancer 84 0.026
329
P GST053 Gastric Cancer 83 0.026
330
MLR004 Malaria 81 0.026
331
P RTT002 Rett Syndrome 80 0.026
332
P RHM011 Rheumatoid Arthritis 80 0.026
333
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.026
334
c NRF023 Neurofibromatosis, Type Ii 80 0.026
335
INS024 Insulin-Like Growth Factor I 79 0.026
336
IMM167 Immune Deficiency Disease 78 0.026
337
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.026
338
KPS004 Kaposi Sarcoma 75 0.026
339
P HRT032 Heart Disease 75 0.026
340
PHN003 Phenylketonuria 75 0.026
341
GLB015 Glioblastoma Multiforme 75 0.026
342
BRN028 Brain Cancer 74 0.026
343
P SCH015 Schizophrenia 74 0.026
344
P OST002 Osteoporosis 74 0.026
345
SVR004 Severe Combined Immunodeficiency 73 0.026
346
c SPN225 Spondyloarthropathy 1 73 0.026
347
ANX010 Anxiety 73 0.026
348
MSC157 Muscular Dystrophy, Duchenne Type 72 0.026
349
P MLT020 Multiple Sclerosis 72 0.026
350
P FML011 Familial Adenomatous Polyposis 72 0.026
351
P AMY004 Amyloidosis 70 0.026
352
GST040 Gastric Adenocarcinoma 70 0.026
353
MLT157 Multiple System Atrophy 1 70 0.026
354
LGH007 Leigh Syndrome 70 0.026
355
P HYP061 Hypertrophic Cardiomyopathy 70 0.026
356
PLY001 Polycythemia Vera 69 0.026
357
P MLN008 Melanoma 69 0.026
358
P ART022 Arthritis 69 0.026
359
SVR097 Severe Cutaneous Adverse Reaction 69 0.026
360
CRB037 Cerebral Palsy 69 0.026
361
P OCL013 Oculodentodigital Dysplasia 69 0.026
362
P HYP086 Hypothyroidism 69 0.026
363
P LKM062 Leukemia, Acute Lymphoblastic 69 0.026
364
P TMP003 Temporal Arteritis 68 0.026
365
P PNM007 Pneumonia 68 0.026
366
P MYS003 Myasthenia Gravis 68 0.026
367
BRN024 Bronchitis 68 0.026
368
CNN005 Connective Tissue Disease 68 0.026
369
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.026
370
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.026
371
c INF071 Inflammatory Bowel Disease 1 67 0.026
372
BRK010 Burkitt Lymphoma 67 0.026
373
P CHR012 Chronic Granulomatous Disease 67 0.026
374
P TRN020 Turner Syndrome 67 0.026
375
P HYP098 Hypereosinophilic Syndrome 67 0.026
376
LPT001 Leptospirosis 66 0.026
377
ALC007 Alcohol Dependence 66 0.026
378
GLN010 Glanzmann Thrombasthenia 66 0.026
379
P NSP012 Nasopharyngeal Carcinoma 66 0.026
380
P MCR115 Microvascular Complications of Diabetes 5 66 0.026
381
c FML346 Familial Adenomatous Polyposis 1 66 0.026
382
HYP056 Hypoglycemia 66 0.026
383
P HYD006 Hydrocephalus 66 0.026
384
P DRM053 Dermatitis, Atopic 66 0.026
385
MYL031 Myeloproliferative Neoplasm 66 0.026
386
c SML038 Small Cell Cancer of the Lung 65 0.026
387
P PLM036 Pulmonary Fibrosis 65 0.026
388
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.026
389
P ART005 Arteriovenous Malformation 65 0.026
390
P CNJ013 Conjunctivitis 65 0.026
391
PPL049 Papillon-Lefevre Syndrome 65 0.026
392
PND002 Pendred Syndrome 65 0.026
393
P PRS038 Personality Disorder 65 0.026
394
P ADL010 Adult Respiratory Distress Syndrome 65 0.026
395
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.026
396
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.026
397
P MST009 Mastocytosis 64 0.026
398
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.026
399
P PRD008 Periodontitis 64 0.026
400
MSC007 Muscle Hypertrophy 64 0.026
401
c DPH024 Diaphragmatic Hernia, Congenital 63 0.026
402
INC021 Incontinentia Pigmenti 63 0.026
403
P HML002 Hemolytic Anemia 63 0.026
404
P ANR048 Aniridia 1 63 0.026
405
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.026
406
TYP007 Typhoid Fever 63 0.026
407
P HYP069 Hyperparathyroidism 63 0.026
408
ACT119 Acute Promyelocytic Leukemia 63 0.026
409
INT146 Intervertebral Disc Disease 63 0.026
410
c SYS004 Systemic Mastocytosis 63 0.026
411
TRN015 Transient Cerebral Ischemia 63 0.026
412
ANR007 Anorexia Nervosa 63 0.026
413
c GLC092 Glaucoma, Primary Open Angle 62 0.026
414
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.026
415
CLT003 Colitis 62 0.026
416
c FNC043 Fanconi Anemia, Complementation Group E 62 0.026
417
c HPT003 Hepatitis a 62 0.026
418
c BRN108 Branchiootic Syndrome 1 62 0.026
419
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.026
420
c SVR001 Severe Acute Respiratory Syndrome 62 0.026
421
P ESP024 Esophagitis 62 0.026
422
P TRC086 Trichohepatoenteric Syndrome 1 62 0.026
423
BLL006 Bullous Pemphigoid 62 0.026
424
CTN007 Cutaneous Leishmaniasis 62 0.026
425
MDD011 Mood Disorder 62 0.026
426
BLD131 Bladder Urothelial Carcinoma 62 0.026
427
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.026
428
OSS012 Osseous Heteroplasia, Progressive 61 0.026
429
ART141 Arteriovenous Malformations of the Brain 61 0.026
430
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.026
431
DRR016 Diarrhea 2, with Microvillus Atrophy 60 0.026
432
DPH001 Diphtheria 60 0.026
433
P SCL018 Scoliosis 60 0.026
434
P VNT002 Ventricular Septal Defect 60 0.026
435
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.026
436
ACN002 Acanthosis Nigricans 60 0.026
437
ACQ007 Acquired Immunodeficiency Syndrome 60 0.026
438
SQM006 Squamous Cell Carcinoma 60 0.026
439
DNG002 Dengue Hemorrhagic Fever 60 0.026
440
VRC005 Varicose Veins 60 0.026
441
P PTN014 Patent Ductus Arteriosus 1 60 0.026
442
ORL011 Oral Cancer 60 0.026
443
INS001 Insulinoma 60 0.026
444
HYD002 Hydronephrosis 60 0.026
445
P BRN019 Bernard-Soulier Syndrome 60 0.026
446
P OPT006 Optic Nerve Disease 60 0.026
447
SPP011 Suppression of Tumorigenicity 12 59 0.026
448
P RBL001 Rubella 59 0.026
449
P BND020 Bone Disease 59 0.026
450
c DNG003 Dengue Disease 59 0.026
451
PRN019 Perinatal Necrotizing Enterocolitis 59 0.026
452
DCT002 Ductal Carcinoma in Situ 59 0.026
453
P BRS044 Breast Adenocarcinoma 59 0.026
454
AVN001 Avian Influenza 59 0.026
455
BRN002 Bronchiolitis 59 0.026
456
ANR040 Aneurysm 59 0.026
457
PST028 Post-Traumatic Stress Disorder 58 0.026
458
P ALC033 Alcohol Use Disorder 58 0.026
459
CNT047 Contact Dermatitis 58 0.026
460
ERY003 Erythema Multiforme 58 0.026
461
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.026
462
P EHL001 Ehlers-Danlos Syndrome 58 0.026
463
EYD002 Eye Disease 58 0.026
464
DSS008 Disease of Mental Health 58 0.026
465
P MMP001 Mumps 58 0.026
466
CNS004 Constipation 58 0.026
467
c DWL002 Dowling-Degos Disease 1 58 0.026
468
P CND004 Candidiasis 58 0.026
469
P PRP019 Peripheral Nervous System Disease 58 0.026
470
GLS018 Glass Syndrome 57 0.026
471
P PLV020 Pelvic Organ Prolapse 57 0.026
472
CHL067 Cholecystitis 57 0.026
473
P PLY041 Polymyositis 57 0.026
474
c MST023 Mesothelioma, Malignant 57 0.026
475
APH001 Aphthous Stomatitis 57 0.026
476
P FCL005 Focal Segmental Glomerulosclerosis 57 0.026
477
CMM005 Common Cold 57 0.026
478
BLR008 Bilirubin Metabolic Disorder 57 0.026
479
SCH014 Schistosomiasis 57 0.026
480
SKN022 Skin Squamous Cell Carcinoma 57 0.026
481
PHR003 Pharyngitis 57 0.026
482
P MYS005 Myositis 56 0.026
483
CMR002 Coumarin Resistance 56 0.026
484
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.026
485
TRN018 Transitional Cell Carcinoma 56 0.026
486
c ACT134 Acute Liver Failure 56 0.026
487
LMY014 Leiomyoma, Uterine 56 0.026
488
PRS047 Prostatitis 56 0.026
489
c BRC078 Brachydactyly, Type A1 56 0.026
490
P NRF002 Neurofibromatosis 56 0.026
491
GST050 Gastrointestinal System Disease 56 0.026
492
ORL005 Oral Candidiasis 56 0.026
493
SLC006 Silicosis 56 0.026
494
ATR057 Atrioventricular Block 55 0.026
495
c FML035 Familial Hyperlipidemia 55 0.026
496
HYP005 Hypokalemia 55 0.026
497
MCL006 Macular Retinal Edema 55 0.026
498
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.026
499
P MLN007 Male Infertility 55 0.026
500
c BCT007 Bacterial Meningitis 55 0.026
501
NPH009 Nephrolithiasis 55 0.026
502
c CTS029 Cutis Laxa, Autosomal Recessive, Type Iiia 55 0.026
503
P ANT006 Antiphospholipid Syndrome 55 0.026
504
DFN344 Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome 55 0.026
505
P PTT006 Pituitary Adenoma 55 0.026
506
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.026
507
OCL020 Ocular Cicatricial Pemphigoid 55 0.026
508
P SBS003 Substance Abuse 55 0.026
509
BRN045 Brunner Syndrome 55 0.026
510
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.026
511
URN010 Urinary Tract Obstruction 55 0.026
512
END040 Endogenous Depression 55 0.026
513
P JNC001 Junctional Epidermolysis Bullosa 54 0.026
514
RSC001 Rosacea 54 0.026
515
ACD008 Acid-Labile Subunit Deficiency 54 0.026
516
P ICH004 Ichthyosis 54 0.026
517
PRT038 Protein-Energy Malnutrition 54 0.026
518
RST011 Restrictive Dermopathy, Lethal 54 0.026
519
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.026
520
THR013 Thoracic Outlet Syndrome 54 0.026
521
AMN001 Amenorrhea 54 0.026
522
SLP001 Sleeping Sickness 54 0.026
523
P TRM003 Tremor 54 0.026
524
CLL003 Cellulitis 54 0.026
525
NNL006 Non-Alcoholic Steatohepatitis 54 0.026
526
P BRC006 Brachydactyly 53 0.026
527
PLM012 Pulmonary Sarcoidosis 53 0.026
528
ABL002 Ablepharon-Macrostomia Syndrome 53 0.026
529
P END047 Endophthalmitis 53 0.026
530
P EPD016 Epidermolysis Bullosa 53 0.026
531
P INS002 in Situ Carcinoma 53 0.026
532
HRT012 Heart Valve Disease 53 0.026
533
P HMC002 Homocystinuria 53 0.026
534
CRH005 Crohn's Colitis 53 0.026
535
ICH054 Ichthyosis, X-Linked 53 0.026
536
P RTN016 Retinal Degeneration 53 0.026
537
MST005 Mastitis 53 0.026
538
CYS005 Cysticercosis 53 0.026
539
INT075 Intracranial Hypertension 53 0.026
540
GST023 Gastric Ulcer 53 0.026
541
DNT012 Dental Caries 53 0.026
542
P RTN022 Retinal Vein Occlusion 53 0.026
543
c HPT007 Hepatitis E 53 0.026
544
PRP080 Peripheral Artery Disease 53 0.026
545
ALC009 Alcoholic Liver Cirrhosis 53 0.026
546
c PSR017 Psoriasis 2 53 0.026
547
P INT068 Intestinal Disease 53 0.026
548
P RTN018 Retinal Disease 53 0.026
549
CHR073 Choreatic Disease 52 0.026
550
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.026
551
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.026
552
LYS002 Lysosomal Storage Disease 52 0.026
553
c VRL010 Viral Hepatitis 52 0.026
554
ACR041 Acromelic Frontonasal Dysostosis 52 0.026
555
DYS015 Dysentery 52 0.026
556
P MSC003 Muscular Atrophy 52 0.026
557
P NRC002 Narcolepsy 52 0.026
558
NRP045 Neuropathy, Ataxia, and Retinitis Pigmentosa 52 0.026
559
c PSR023 Psoriasis 1 52 0.026
560
BWN001 Bowen-Conradi Syndrome 52 0.026
561
PTH003 Pathologic Nystagmus 52 0.026
562
HYP014 Hyperuricemia 52 0.026
563
ART074 Aortic Dissection 52 0.026
564
LMY002 Leiomyoma 52 0.026
565
SPN051 Spondylitis 51 0.026
566
SPS003 Spastic Diplegia 51 0.026
567
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.026
568
FDL002 Food Allergy 51 0.026
569
ILS001 Ileus 51 0.026
570
ANK001 Ankylosis 51 0.026
571
c PRM108 Primary Progressive Multiple Sclerosis 51 0.026
572
CYS014 Cystadenocarcinoma 51 0.026
573
CCC002 Coccidiosis 51 0.026
574
P PRC012 Pericardial Effusion 51 0.026
575
P THR015 Thrombophilia 51 0.026
576
c VRL007 Viral Encephalitis 51 0.026
577
CCT002 Cicatricial Pemphigoid 51 0.026
578
P RNL007 Renal Tubular Acidosis 51 0.026
579
c BRC051 Brachydactyly, Type B1 51 0.026
580
c SCN007 Secondary Hyperparathyroidism 51 0.026
581
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.026
582
c BRC079 Brachydactyly, Type A2 51 0.026
583
c EHL078 Ehlers-Danlos Syndrome, Kyphoscoliotic Type, 1 51 0.026
584
HYP781 Hypoascorbemia 51 0.026
585
c RBN018 Robinow Syndrome, Autosomal Dominant 1 51 0.026
586
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.026
587
HYP081 Hypolipoproteinemia 51 0.026
588
P MMB011 Membranous Nephropathy 50 0.026
589
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.026
590
P OVR082 Overgrowth Syndrome 50 0.026
591
P BRT029 Brittle Cornea Syndrome 2 50 0.026
592
PST021 Postpartum Depression 50 0.026
593
c SVR005 Severe Pre-Eclampsia 50 0.026
594
TRY001 Trypanosomiasis 50 0.026
595
P KRT007 Keratoconus 50 0.026
596
HRT011 Heart Septal Defect 50 0.026
597
c INF023 Inflammatory Breast Carcinoma 50 0.026
598
P ATR005 Atrophic Gastritis 50 0.026
599
DBT004 Diabetic Polyneuropathy 49 0.026
600
ADR038 Adermatoglyphia 49 0.026
601
KRT001 Keratoconjunctivitis Sicca 49 0.026
602
BLL004 Bullous Keratopathy 49 0.026
603
MCN001 Mucinous Adenocarcinoma 49 0.026
604
VLV047 Volvulus of Midgut 49 0.026
605
PLP001 Pulpitis 49 0.026
606
CCN002 Cocaine Abuse 49 0.026
607
P OPN001 Open-Angle Glaucoma 49 0.026
608
P RBN002 Robinow Syndrome 49 0.026
609
STP011 Stapes Ankylosis with Broad Thumbs and Toes 49 0.026
610
URM002 Uremia 49 0.026
611
c DSB006 Desbuquois Dysplasia 1 48 0.026
612
NRL018 Neural Tube Defects, Folate-Sensitive 48 0.026
613
CCN001 Cocaine Dependence 48 0.026
614
VTM033 Vitamin K Deficiency Bleeding 48 0.026
615
DPN005 Du Pan Syndrome 48 0.026
616
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.026
617
SPL018 Splenomegaly 48 0.026
618
HMP001 Hemopericardium 48 0.026
619
TBR011 Tuberculous Meningitis 48 0.026
620
RCT020 Rectum Adenocarcinoma 48 0.026
621
OPD006 Opioid Addiction 48 0.026
622
c HYD064 Hydrocephalus, Congenital, 1 48 0.026
623
SXL003 Sexual Disorder 47 0.026
624
PRP007 Priapism 47 0.026
625
DRG003 Drug Dependence 47 0.026
626
P CRN028 Corneal Ulcer 47 0.026
627
KRT008 Keratopathy 47 0.026
628
AST006 Astigmatism 47 0.026
629
c PSR032 Psoriasis 11 47 0.026
630
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.026
631
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.026
632
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.026
633
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.026
634
P CRC039 Coarctation of Aorta 47 0.026
635
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.026
636
ASP004 Asphyxia Neonatorum 46 0.026
637
RTN020 Retinal Vascular Disease 46 0.026
638
CLN045 Colonic Benign Neoplasm 46 0.026
639
P BRB001 Beriberi 46 0.026
640
P PLL002 Pellagra 46 0.026
641
P BNG032 Benign Mesothelioma 46 0.026
642
c RBN017 Robinow Syndrome, Autosomal Dominant 2 46 0.026
643
CRN019 Coronary Artery Vasospasm 46 0.026
644
P PRX021 Proximal Symphalangism 46 0.026
645
LKS001 Leukostasis 46 0.026
646
c DRR009 Diarrhea 6 46 0.026
647
ANR004 Anuria 46 0.026
648
PLC001 Placenta Accreta 46 0.026
649
TRT001 Teratocarcinoma 45 0.026
650
NWC001 Newcastle Disease 45 0.026
651
SYN005 Synostosis 45 0.026
652
P SBR004 Seborrheic Dermatitis 45 0.026
653
MYF001 Myofibroma 45 0.026
654
SBC016 Subacute Delirium 44 0.026
655
DBT008 Diabetic Angiopathy 44 0.026
656
APP009 Appendix Adenocarcinoma 44 0.026
657
GRN017 Granulocytopenia 44 0.026
658
IMM064 Immunodeficiency, Common Variable, 10 44 0.026
659
ORG002 Organic Acidemia 44 0.026
660
CNN002 Cannabis Abuse 44 0.026
661
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.026
662
KWS001 Kwashiorkor 44 0.026
663
c HYP272 Hypercholesterolemia, Familial, 3 44 0.026
664
HPT082 Hepatic Adenomas, Familial 44 0.026
665
P CRN024 Corneal Disease 44 0.026
666
P HYP121 Hypoalphalipoproteinemia 43 0.026
667
SKN005 Skin Atrophy 43 0.026
668
ECC004 Eccrine Porocarcinoma 43 0.026
669
c CHR096 Chronic Pulmonary Heart Disease 43 0.026
670
MGS001 Megaesophagus 43 0.026
671
c SRC023 Sarcoidosis 2 43 0.026
672
PLY068 Polysubstance Abuse 43 0.026
673
PRS042 Prostate Disease 43 0.026
674
P PRP034 Purpura Fulminans 43 0.026
675
TRP009 Triple X Syndrome 42 0.026
676
PNM013 Pneumococcal Meningitis 42 0.026
677
c RTN047 Retinitis Pigmentosa 18 42 0.026
678
BRC004 Brachydactyly-Syndactyly Syndrome 42 0.026
679
c PSR028 Psoriasis 7 42 0.026
680
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.026
681
P DST107 Distal Renal Tubular Acidosis 42 0.026
682
TRS002 Tarsal-Carpal Coalition Syndrome 42 0.026
683
ATX019 Ataxia with Vitamin E Deficiency 42 0.026
684
c MLG079 Malignant Pleural Mesothelioma 42 0.026
685
BNB002 Bainbridge-Ropers Syndrome 42 0.026
686
MYF002 Myofascial Pain Syndrome 42 0.026
687
FSC002 Fascioliasis 42 0.026
688
c CTR132 Cataract 3, Multiple Types 41 0.026
689
EPC002 Epicondylitis 41 0.026
690
c ATS082 Autosomal Dominant Robinow Syndrome 41 0.026
691
XRP001 Xerophthalmia 41 0.026
692
MMM006 Mammographic Density 41 0.026
693
c PSR018 Psoriasis 13 41 0.026
694
PRS063 Paresthesia 41 0.026
695
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.026
696
DHY010 Dihydrolipoamide Dehydrogenase Deficiency 40 0.026
697
THR035 Thrombasthenia 40 0.026
698
ANX004 Anoxia 40 0.026
699
MCN008 Mucinous Cystadenocarcinoma 40 0.026
700
CNS002 Constrictive Pericarditis 40 0.026
701
HPR006 Heparin Cofactor Ii Deficiency 40 0.026
702
FNG016 Fungal Keratitis 40 0.026
703
HYP030 Hypoactive Sexual Desire Disorder 40 0.026
704
P PRG092 Pregnancy Loss, Recurrent 1 40 0.026
705
PLY100 Polyploidy 40 0.026
706
CNN001 Cannabis Dependence 40 0.026
707
ART008 Arteriosclerosis Obliterans 40 0.026
708
WND001 Wound Botulism 39 0.026
709
c CTR130 Cataract 9, Multiple Types 39 0.026
710
PCH007 Pouchitis 39 0.026
711
ADP007 Adie Pupil 39 0.026
712
P MLT072 Multiple Synostoses Syndrome 39 0.026
713
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.026
714
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.026
715
c SYS043 Systemic Lupus Erythematosus 1 38 0.026
716
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.026
717
HPT070 Hepatosplenic T-Cell Lymphoma 38 0.026
718
CRT004 Carotid Artery Thrombosis 38 0.026
719
CNT060 Central Serous Chorioretinopathy 38 0.026
720
FRS019 Farsightedness 38 0.026
721
c BRC080 Brachydactyly, Type A1, B 38 0.026
722
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.026
723
P FML187 Familial Hypertension 37 0.026
724
ATM052 Autoimmune Disease 1 37 0.026
725
GLM044 Glomerular Disease 37 0.026
726
CRN022 Corneal Degeneration 36 0.026
727
GRN055 Granular Corneal Dystrophy 36 0.026
728
SYN086 Synostoses, Tarsal, Carpal, and Digital 35 0.026
729
BRK012 Broken Heart Syndrome 35 0.026
730
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.026
731
BCL014 B-Cell Growth Factor 35 0.026
732
ATX010 Ataxia Neuropathy Spectrum 34 0.026
733
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 34 0.026
734
ACT064 Acute Necrotizing Encephalitis 33 0.026
735
P VSC018 Visceral Steatosis 33 0.026
736
c KRT029 Keratoconus 1 33 0.026
737
HND015 Hand Skill, Relative 33 0.026
738
c BRC099 Brachydactyly, Type A4 32 0.026
739
c BRC075 Brachydactyly, Type A1, C 32 0.026
740
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.026
741
P SCL047 Sclerocornea 32 0.026
742
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.026
743
INF009 Inflammatory Spondylopathy 31 0.026
744
DRF001 Dirofilariasis 31 0.026
745
GST007 Gastric Dilatation 31 0.026
746
SGR001 Sugarman Brachydactyly 30 0.026
747
ERY066 Erythema Multiforme Major 30 0.026
748
ERY069 Erythrokeratoderma ''en Cocardes'' 30 0.026
749
IRR001 Irregular Astigmatism 30 0.026
751
GNT019 Giant Cell Myocarditis 30 0.026
752
PRN008 Peroneal Nerve Paralysis 29 0.026
753
PRN035 Perniosis 28 0.026
755
CRC001 Cercarial Dermatitis 28 0.026
756
c FTL067 Fetal Hemoglobin Quantitative Trait Locus 6 28 0.026
757
CLN002 Colon Mucinous Adenocarcinoma 28 0.026
758
ARG004 Argyria 27 0.026
759
HNM002 Hinman Syndrome 27 0.026
760
HYP855 Hyperpigmentation of the Skin 27 0.026
761
URN022 Urinary Tract Infections, Recurrent 27 0.026
762
MLR020 Malaria, Mild 27 0.026
763
CTR014 Cataract Microcornea Syndrome 26 0.026
764
PRQ002 Paraquat Poisoning 26 0.026
765
c CRD150 Cardiomyopathy, Familial Hypertrophic, 18 26 0.026
766
CNR001 Coenurosis 25 0.026
767
ADG002 Audiogenic Seizures 25 0.026
768
SYM024 Symphalangism, Distal 22 0.026
769
FNG003 Fungal Esophagitis 22 0.026
770
PLL009 Pellucid Marginal Degeneration 22 0.026
771
c BLD123 Bleeding Disorder, Platelet-Type, 13 22 0.026
773
c PST001 Posterior Myocardial Infarction 21 0.026
774
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 0.026
775
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 19 0.026
776
P TLN014 Tl Antigen 19 0.026
777
PRL045 Proline-Negative Auxotroph of Hamster, Complementation of 18 0.026
778
P RSS029 Resistance to Thyroid Hormone Due to a Mutation in Thyroid Hormone Receptor Alpha 16 0.026
779
BLD137 Blood Group--Ahonen 16 0.026
780
MYC004 Mycotic Corneal Ulcer 14 0.026
781
P EST010 Esterase B 14 0.026
Content
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