Search results for Pyridoxine

835 hits were found for Pyridoxine

# Family MCID Name MIFTS Score
1
EPL131 Epilepsy, Pyridoxine-Dependent 49 10.200
2
c ANM033 Anemia, Sideroblastic, 2, Pyridoxine-Refractory 23 5.396
3
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 45 5.010
4
PYR016 Pyridoxine Deficiency 30 4.913
5
c ANM039 Anemia, Sideroblastic, Pyridoxine-Responsive, Autosomal Recessive 19 4.633
6
P PYR006 Pyridoxine-Responsive Sideroblastic Anemia 17 4.151
7
c ANM032 Anemia, Sideroblastic, 3, Pyridoxine-Refractory 25 4.084
8
PYR009 Pyridoxine Deficiency Anemia 34 3.136
9
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 52 3.051
10
PYR021 Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency 47 3.009
11
c ANM036 Anemia, Sideroblastic, 1 57 2.225
12
c ATS408 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 3 4 2.072
13
DSR075 Disorder of Pyridoxine Metabolism 4 2.072
14
P SZR006 Seizure Disorder 56 0.326
15
VSL002 Visual Epilepsy 59 0.322
16
P EPL164 Epilepsy 71 0.258
17
DFC004 Deficiency Anemia 70 0.233
18
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.233
19
P NRP001 Neuropathy 56 0.225
20
P HMC002 Homocystinuria 53 0.199
21
ATS010 Autosomal Recessive Disease 48 0.155
22
P SDR003 Sideroblastic Anemia 49 0.153
23
STT001 Status Epilepticus 60 0.149
24
P PRP019 Peripheral Nervous System Disease 58 0.149
25
SNS003 Sensory Peripheral Neuropathy 54 0.149
26
P PRM002 Primary Hyperoxaluria 62 0.130
27
WST001 West Syndrome 61 0.125
28
CRP001 Carpal Tunnel Syndrome 67 0.122
29
P ENC018 Encephalopathy 61 0.122
30
HMC014 Homocysteinemia 53 0.117
31
PLM001 Pulmonary Tuberculosis 69 0.114
32
c HYP794 Hyperoxaluria, Primary, Type I 63 0.102
33
PRM020 Premenstrual Tension 40 0.099
34
IMM167 Immune Deficiency Disease 78 0.096
35
P MYC084 Mycobacterium Tuberculosis 1 68 0.096
36
RBF001 Riboflavin Deficiency 49 0.096
37
HMN044 Human Immunodeficiency Virus Type 1 71 0.092
38
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.088
39
P HYP035 Hypophosphatasia 61 0.088
40
ACQ007 Acquired Immunodeficiency Syndrome 60 0.088
41
IRN002 Iron Metabolism Disease 57 0.088
42
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.088
43
URL001 Urolithiasis 45 0.088
44
P HYP265 Hypotonia 43 0.088
45
ATH013 Atherosclerosis Susceptibility 65 0.085
46
DPR016 Depression 63 0.085
47
OCL069 Ocular Motor Apraxia 51 0.085
48
ALC007 Alcohol Dependence 66 0.081
49
P TRC086 Trichohepatoenteric Syndrome 1 62 0.081
50
DRM006 Dermatitis 61 0.081
51
P PLY019 Polyneuropathy 56 0.081
52
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.081
53
P RRH023 Rare Hereditary Hemochromatosis 41 0.081
54
c HMC039 Hemochromatosis, Type 1 74 0.077
55
P KDN018 Kidney Disease 72 0.077
56
P LKM062 Leukemia, Acute Lymphoblastic 69 0.077
57
AMN001 Amenorrhea 54 0.077
58
MTB004 Metabolic Acidosis 50 0.077
59
P LKM002 Leukemia 68 0.072
60
P DBT009 Diabetes Mellitus 64 0.072
61
c HYP292 Hypophosphatasia, Infantile 57 0.072
62
NPH009 Nephrolithiasis 55 0.072
63
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.072
64
TRD006 Tardive Dyskinesia 54 0.072
65
THR013 Thoracic Outlet Syndrome 54 0.072
66
LYM019 Lymphosarcoma 46 0.072
67
CYS019 Cystathioninuria 45 0.072
68
P SCH015 Schizophrenia 74 0.068
69
P LYM118 Lymphoma 68 0.068
70
P LVR013 Liver Disease 68 0.068
71
c RHB024 Rhabdomyosarcoma 2 67 0.068
72
ALL026 Allergic Hypersensitivity Disease 62 0.068
73
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.068
74
P CTR002 Cataract 60 0.068
75
HMS001 Hemosiderosis 54 0.068
76
END086 End Stage Renal Disease 51 0.068
77
RFR010 Refractory Anemia 48 0.068
78
GLC096 Galactorrhea 42 0.068
79
P LNG032 Lung Cancer 98 0.063
80
P ATX030 Ataxia-Telangiectasia 82 0.063
81
P MYC007 Myocardial Infarction 70 0.063
82
MYL005 Myelofibrosis 70 0.063
83
ART001 Arterial Tortuosity Syndrome 66 0.063
84
AND002 Androgen Insensitivity Syndrome 66 0.063
85
P HYD006 Hydrocephalus 66 0.063
86
TTN003 Tetanus 65 0.063
87
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.063
88
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.063
89
HYP020 Hyperprolactinemia 64 0.063
90
P NTR004 Neutropenia 63 0.063
91
P VSC007 Vascular Disease 63 0.063
92
P CRN300 Coronary Heart Disease 1 63 0.063
93
P MVM001 Movement Disease 63 0.063
94
FTT001 Fatty Liver Disease 61 0.063
95
ACN002 Acanthosis Nigricans 60 0.063
96
P AXN002 Axenfeld-Rieger Syndrome 59 0.063
97
GYR004 Gyrate Atrophy of Choroid and Retina 57 0.063
98
P ALP106 Alport Syndrome 1, X-Linked 55 0.063
99
DBT010 Diabetic Neuropathy 54 0.063
100
P SBR004 Seborrheic Dermatitis 45 0.063
101
ALR002 Al-Raqad Syndrome 33 0.063
102
c HYP595 Hypertension, Essential 84 0.057
103
NRL016 Neural Tube Defects 82 0.057
104
STR067 Stroke, Ischemic 81 0.057
105
P RHM011 Rheumatoid Arthritis 80 0.057
106
P PRK057 Parkinson Disease, Late-Onset 78 0.057
107
P HRT032 Heart Disease 75 0.057
108
PHN003 Phenylketonuria 75 0.057
109
c HYP836 Hypercholesterolemia, Familial, 1 73 0.057
110
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.057
111
ADL002 Adult Syndrome 70 0.057
112
LYM133 Lymphoma, Hodgkin, Classic 69 0.057
113
P HYP086 Hypothyroidism 69 0.057
114
P HPT021 Hepatitis 67 0.057
115
CRB039 Cerebrovascular Disease 67 0.057
116
c MGR028 Migraine with or Without Aura 1 67 0.057
117
HYP056 Hypoglycemia 66 0.057
118
SRC014 Sarcoma 65 0.057
119
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.057
120
P ANR048 Aniridia 1 63 0.057
121
ANR007 Anorexia Nervosa 63 0.057
122
LPP008 Lipoprotein Quantitative Trait Locus 62 0.057
123
NTR005 Nutritional Deficiency Disease 62 0.057
124
HYP066 Hyperglycemia 61 0.057
125
P MCR010 Microcephaly 59 0.057
126
ADN018 Adenoma 59 0.057
127
PPT005 Peptic Ulcer Disease 59 0.057
128
MNT002 Mental Depression 58 0.057
129
P CRD246 Cardiovascular System Disease 57 0.057
130
HYP266 Hypoxia 57 0.057
131
CMR002 Coumarin Resistance 56 0.057
132
P ART021 Arteriosclerosis 54 0.057
133
P PTS002 Ptosis 53 0.057
134
SPN035 Spindle Cell Sarcoma 53 0.057
135
DNT012 Dental Caries 53 0.057
136
ART140 Arteries, Anomalies of 52 0.057
137
NPH003 Nephrocalcinosis 51 0.057
138
P LCT001 Lactic Acidosis 51 0.057
139
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.057
140
P SCK005 Sickle Cell Disease 50 0.057
141
c MCR120 Microvascular Complications of Diabetes 7 47 0.057
142
KRT002 Keratomalacia 47 0.057
143
GRN017 Granulocytopenia 44 0.057
144
48X005 48,xyyy 39 0.057
145
ATX010 Ataxia Neuropathy Spectrum 34 0.057
146
ACT064 Acute Necrotizing Encephalitis 33 0.057
147
TTN001 Tetanus Neonatorum 29 0.057
148
CHL079 Children's Interstitial Lung Disease 26 0.057
149
c ATS210 Autosomal Recessive Sideroblastic Anemia 26 0.057
150
ADG002 Audiogenic Seizures 25 0.057
151
BLD137 Blood Group--Ahonen 16 0.057
152
FLN005 Folinic Acid-Responsive Seizures 11 0.057
153
P OVR042 Ovarian Cancer 88 0.051
154
MYL069 Myeloma, Multiple 85 0.051
155
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.051
156
c SPN225 Spondyloarthropathy 1 73 0.051
157
P GRF003 Graft-Versus-Host Disease 72 0.051
158
MYL009 Myelodysplastic Syndrome 70 0.051
159
DWN001 Down Syndrome 70 0.051
160
c CHR684 Chronic Kidney Disease 70 0.051
161
CNG034 Congestive Heart Failure 69 0.051
162
P ART022 Arthritis 69 0.051
163
P ANG001 Angelman Syndrome 69 0.051
164
RCK004 Rickets 68 0.051
165
P THR014 Thrombocytopenia 67 0.051
166
PSY004 Psychotic Disorder 67 0.051
167
P CLC063 Celiac Disease 1 66 0.051
168
ANG054 Angina Pectoris 66 0.051
169
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.051
170
P DYS154 Dystonia 65 0.051
171
BRR014 Barrett Esophagus 65 0.051
172
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.051
173
LVR012 Liver Cirrhosis 62 0.051
174
P PRP029 Porphyria 62 0.051
175
GST033 Gestational Diabetes 61 0.051
176
P LPS004 Lupus Erythematosus 61 0.051
177
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.051
178
ISC004 Ischemia 58 0.051
179
P BCL017 B-Cell Lymphoma 58 0.051
180
P ALC033 Alcohol Use Disorder 58 0.051
181
DSS008 Disease of Mental Health 58 0.051
182
THR024 Thrombosis 57 0.051
183
AYM001 Ayme-Gripp Syndrome 57 0.051
184
P BPL003 Bipolar Disorder 56 0.051
185
SCH003 Schizophreniform Disorder 56 0.051
186
AGN016 Aging 56 0.051
187
CRC006 Carcinoid Syndrome 55 0.051
188
P TRM003 Tremor 54 0.051
189
TXC002 Toxic Encephalopathy 53 0.051
190
PRN011 Pernicious Anemia 53 0.051
191
PRP080 Peripheral Artery Disease 53 0.051
192
c MCR113 Microvascular Complications of Diabetes 3 52 0.051
193
NRT004 Neuritis 52 0.051
194
PLS009 Plasma Cell Neoplasm 51 0.051
195
MGL001 Megaloblastic Anemia 51 0.051
196
BHR001 Behr Syndrome 51 0.051
197
HYP781 Hypoascorbemia 51 0.051
198
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.051
199
URM002 Uremia 49 0.051
200
NRL018 Neural Tube Defects, Folate-Sensitive 48 0.051
201
VTM002 Vitamin B12 Deficiency 48 0.051
202
ATN005 Autonomic Dysfunction 46 0.051
203
P BRB001 Beriberi 46 0.051
204
c PRM038 Primary Agammaglobulinemia 44 0.051
205
c HYP597 Hyperprolinemia, Type Ii 43 0.051
206
P MJR007 Major Affective Disorder 1 43 0.051
207
c MCR130 Microvascular Complications of Diabetes 6 41 0.051
208
c MCR133 Microvascular Complications of Diabetes 4 41 0.051
209
c MJR024 Major Affective Disorder 9 41 0.051
210
OVR094 Ovarian Epithelial Cancer 38 0.051
211
c MJR022 Major Affective Disorder 8 38 0.051
212
c MJR008 Major Affective Disorder 2 35 0.051
213
c MJR023 Major Affective Disorder 7 33 0.051
214
PPL052 Papillomatosis, Confluent and Reticulated 33 0.051
215
c MJR003 Major Affective Disorder 6 33 0.051
216
c MJR006 Major Affective Disorder 5 33 0.051
217
MYC088 Mycobacterium Avium Complex Infections 29 0.051
218
c MJR004 Major Affective Disorder 4 28 0.051
219
NDD001 Nodding Syndrome 21 0.051
220
AND005 Androgen Insensitivity Syndrome, Mild 19 0.051
221
HMC030 Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency 13 0.051
222
P HPT023 Hepatocellular Carcinoma 100 0.044
223
P BRS047 Breast Cancer 97 0.044
224
P ALZ034 Alzheimer Disease 88 0.044
225
c FNC027 Fanconi Anemia, Complementation Group a 81 0.044
226
P BLD134 Bladder Cancer 79 0.044
227
END057 Endometrial Cancer 74 0.044
228
CRH001 Crohn's Disease 74 0.044
229
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.044
230
c THR092 Thrombophilia Due to Thrombin Defect 73 0.044
231
P MLT020 Multiple Sclerosis 72 0.044
232
c LKM063 Leukemia, Chronic Myeloid 72 0.044
233
P ATS364 Autism 70 0.044
234
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.044
235
P TRN020 Turner Syndrome 67 0.044
236
c MCR129 Microvascular Complications of Diabetes 1 66 0.044
237
MYL031 Myeloproliferative Neoplasm 66 0.044
238
c SML038 Small Cell Cancer of the Lung 65 0.044
239
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.044
240
KRT019 Keratitis, Hereditary 65 0.044
241
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.044
242
c PRC016 Pre-Eclampsia 63 0.044
243
c MLG084 Malignant Fibrous Histiocytoma 63 0.044
244
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.044
245
P ACR001 Aicardi-Goutieres Syndrome 62 0.044
246
GLY010 Glycine Encephalopathy 62 0.044
247
MSL001 Measles 62 0.044
248
P SJG008 Sjogren Syndrome 61 0.044
249
P MYL006 Myeloid Leukemia 60 0.044
250
P THL005 Thalassemia 60 0.044
251
IRN001 Iron Deficiency Anemia 59 0.044
252
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.044
253
CNT047 Contact Dermatitis 58 0.044
254
CNS004 Constipation 58 0.044
255
c CHR417 Chronic Graft Versus Host Disease 57 0.044
256
P HDC001 Headache 57 0.044
257
c ACT075 Acute Myocardial Infarction 57 0.044
258
P PRV006 Pervasive Developmental Disorder 57 0.044
259
GLT035 Glutaric Acidemia I 57 0.044
260
P FBR017 Fibrosarcoma 56 0.044
261
HMG005 Hemoglobinopathy 56 0.044
262
P DRR001 Diarrhea 55 0.044
263
DFF005 Diffuse Large B-Cell Lymphoma 55 0.044
264
P HYP076 Hyperthyroidism 55 0.044
265
INT007 Intermediate Coronary Syndrome 55 0.044
266
PRT038 Protein-Energy Malnutrition 54 0.044
267
c XNT010 Xanthinuria, Type I 53 0.044
268
P FBR031 Febrile Seizures 53 0.044
269
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.044
270
ONC002 Onchocerciasis 52 0.044
271
P ECL001 Eclampsia 50 0.044
272
PLC008 Placenta Disease 50 0.044
273
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.044
274
VLV047 Volvulus of Midgut 49 0.044
275
DFN270 Deafness, Dystonia, and Cerebral Hypomyelination 48 0.044
276
c HYD064 Hydrocephalus, Congenital, 1 48 0.044
277
RTC005 Reticulosarcoma 47 0.044
278
c INH020 Inherited Metabolic Disorder 47 0.044
279
ASP004 Asphyxia Neonatorum 46 0.044
280
KRT013 Keratolytic Winter Erythema 46 0.044
281
c DRR009 Diarrhea 6 46 0.044
282
P HYP111 Hyperprolinemia 44 0.044
283
HPT082 Hepatic Adenomas, Familial 44 0.044
284
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.044
285
PHY002 Physical Disorder 42 0.044
286
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.044
287
DBT002 Diabetic Autonomic Neuropathy 41 0.044
288
CHL045 Choline Deficiency Disease 39 0.044
289
PMP002 Pemphigoid Gestationis 39 0.044
290
ADP007 Adie Pupil 39 0.044
291
c CHR682 Chronic Bilirubin Encephalopathy 39 0.044
292
HYP001 Hypochromic Microcytic Anemia 38 0.044
293
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.044
295
c BLD140 Blood Group, I System 32 0.044
296
P CRN133 Coronary Artery Disease, Autosomal Dominant, 1 32 0.044
297
HNM002 Hinman Syndrome 27 0.044
298
MLG164 Malignant Epithelial Tumor of Ovary 26 0.044
299
BLD163 Blood Group, Dombrock System 24 0.044
300
HYP690 Hyper-Beta-Alaninemia 24 0.044
301
BRN040 Bronchus Adenoma 23 0.044
302
c INF185 Infantile Epilepsy Syndrome 22 0.044
303
EPL166 Epilepsy, Early-Onset, Vitamin B6-Dependent 22 0.044
304
ORN004 Ornithinemia 17 0.044
305
P CLR023 Colorectal Cancer 99 0.036
306
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.036
307
c SYS001 Systemic Lupus Erythematosus 86 0.036
308
P PNC035 Pancreatic Cancer 84 0.036
309
MLR004 Malaria 81 0.036
310
c NRF023 Neurofibromatosis, Type Ii 80 0.036
311
AST005 Asthma 76 0.036
312
P RSP003 Respiratory Failure 74 0.036
313
SCK003 Sickle Cell Anemia 74 0.036
314
P OST002 Osteoporosis 74 0.036
315
c BTT014 Beta-Thalassemia 74 0.036
316
ANX010 Anxiety 73 0.036
317
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.036
318
P NRB001 Neuroblastoma 72 0.036
319
WLS001 Wilson Disease 71 0.036
320
PRP027 Peripheral Vascular Disease 71 0.036
321
P PNM007 Pneumonia 68 0.036
322
FLL027 Fallopian Tube Carcinoma 67 0.036
323
P MCR115 Microvascular Complications of Diabetes 5 66 0.036
324
P MNN013 Meningitis 66 0.036
325
P NRV007 Nervous System Disease 66 0.036
326
PRP001 Propionic Acidemia 65 0.036
327
PND002 Pendred Syndrome 65 0.036
328
c DBT099 Diabetes Mellitus, Type I 65 0.036
329
CLF027 Cleft Palate, Isolated 64 0.036
330
PRP083 Porphyria, Acute Intermittent 64 0.036
331
PLM031 Poliomyelitis 64 0.036
332
TYP007 Typhoid Fever 63 0.036
333
LPD008 Lipid Metabolism Disorder 62 0.036
334
P PSR002 Psoriasis 62 0.036
335
c HPT003 Hepatitis a 62 0.036
336
c GLY004 Glycogen Storage Disease V 62 0.036
337
ATM095 Autoimmune Disease 62 0.036
338
TXC005 Toxic Shock Syndrome 62 0.036
339
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.036
340
c PNS012 Paine Syndrome 61 0.036
341
c SCL052 Scleroderma, Familial Progressive 61 0.036
342
ALC006 Alcoholic Hepatitis 61 0.036
343
P NPH012 Nephrotic Syndrome 60 0.036
344
SQM006 Squamous Cell Carcinoma 60 0.036
345
PRT013 Portal Hypertension 59 0.036
346
P BND020 Bone Disease 59 0.036
347
PLM033 Pulmonary Embolism 59 0.036
348
c ACT073 Acute Leukemia 58 0.036
349
FBR047 Fibromyalgia 58 0.036
350
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.036
351
APP015 Apparent Mineralocorticoid Excess 58 0.036
352
P RHN004 Rhinitis 57 0.036
353
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.036
354
ERY051 Erythroleukemia, Familial 56 0.036
355
ALL010 Allergic Contact Dermatitis 56 0.036
356
P ISL078 Isolated Ectopia Lentis 56 0.036
357
P AGN002 Agnosia 55 0.036
358
ICH001 Ichthyosis Vulgaris 55 0.036
359
P ANT006 Antiphospholipid Syndrome 55 0.036
360
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.036
361
P VNS003 Venous Insufficiency 55 0.036
362
END040 Endogenous Depression 55 0.036
363
GLC003 Glucose Intolerance 54 0.036
364
P INF037 Inflammatory Bowel Disease 54 0.036
365
LYM040 Lymphoblastic Lymphoma 54 0.036
366
ABL002 Ablepharon-Macrostomia Syndrome 53 0.036
367
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.036
368
c GLL024 Gallbladder Disease 1 53 0.036
369
c HYP293 Hypophosphatasia, Adult 52 0.036
370
PST011 Pustulosis of Palm and Sole 52 0.036
371
P DDN001 Duodenal Ulcer 52 0.036
372
P RCT021 Rectum Cancer 52 0.036
373
P NRC002 Narcolepsy 52 0.036
374
P THY032 Thyroiditis 52 0.036
375
APR001 Apraxia 52 0.036
376
ARM002 Aromatic L-Amino Acid Decarboxylase Deficiency 52 0.036
377
P MGR003 Migraine with Aura 52 0.036
378
PNG002 Pain Agnosia 51 0.036
379
P THR015 Thrombophilia 51 0.036
380
c ACT078 Acute Porphyria 51 0.036
381
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.036
382
STM007 Stomatitis 50 0.036
383
PPL021 Papilledema 49 0.036
384
c CHR431 Chronic Venous Insufficiency 49 0.036
385
47X002 47,xyy 49 0.036
386
P CTN015 Cutaneous T Cell Lymphoma 49 0.036
387
LRN003 Learning Disability 49 0.036
388
ANT018 Anthracosis 48 0.036
389
MCR018 Microcytic Anemia 47 0.036
390
CRC014 Carcinoid Tumors, Intestinal 47 0.036
391
RTN023 Retinitis 46 0.036
392
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.036
393
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 46 0.036
394
P PLL002 Pellagra 46 0.036
395
OBS004 Obstructive Hydrocephalus 46 0.036
396
P MYC033 Myoclonus 46 0.036
397
ATN004 Autonomic Neuropathy 45 0.036
398
SBC016 Subacute Delirium 44 0.036
399
ORG002 Organic Acidemia 44 0.036
400
KWS001 Kwashiorkor 44 0.036
401
PPL001 Papillary Adenoma 44 0.036
402
c HYP272 Hypercholesterolemia, Familial, 3 44 0.036
403
CYT002 Cytokine Deficiency 42 0.036
404
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.036
405
BCK006 Back Pain 42 0.036
406
MYF002 Myofascial Pain Syndrome 42 0.036
407
NRR001 Neuroretinitis 42 0.036
408
PRS063 Paresthesia 41 0.036
409
c MCR112 Microvascular Complications of Diabetes 2 41 0.036
410
MLY001 Molybdenum Cofactor Deficiency 40 0.036
411
ANG049 Angioedema Induced by Ace Inhibitors 40 0.036
412
c OVR114 Ovarian Cancer 1 38 0.036
413
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.036
414
CRT012 Cortical Blindness 37 0.036
415
P ADT009 Auditory Neuropathy Spectrum Disorder 36 0.036
416
VSL003 Visual Agnosia 34 0.036
417
NRN002 Neuronitis 32 0.036
418
BLP006 Blepharoconjunctivitis 31 0.036
419
c EPL249 Epileptic Encephalopathy, Early Infantile, 82 23 0.036
420
P HYD015 Hydroa Vacciniforme 22 0.036
421
AMN015 Amenorrhea-Galactorrhea Syndrome 21 0.036
422
MNS015 Monosodium Glutamate Sensitivity 20 0.036
423
ANG010 Angular Blepharoconjunctivitis 11 0.036
424
P PRS040 Prostate Cancer 97 0.026
425
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.026
427
c LKM061 Leukemia, Acute Myeloid 84 0.026
428
P RTN008 Retinitis Pigmentosa 79 0.026
429
P LKM071 Leukemia, Chronic Lymphocytic 79 0.026
430
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.026
431
c ATR087 Atrial Standstill 1 75 0.026
432
SVR004 Severe Combined Immunodeficiency 73 0.026
433
P CNR004 Cone-Rod Dystrophy 2 73 0.026
434
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.026
435
P HNT016 Huntington Disease 72 0.026
436
ACR007 Acromegaly 71 0.026
437
c EPL184 Epileptic Encephalopathy, Early Infantile, 6 70 0.026
438
P FRG001 Fragile X Syndrome 70 0.026
439
P TBR001 Tuberous Sclerosis 70 0.026
440
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.026
441
CRB037 Cerebral Palsy 69 0.026
442
P OCL013 Oculodentodigital Dysplasia 69 0.026
443
P LPR021 Leprosy 3 69 0.026
444
P SYS005 Systemic Scleroderma 68 0.026
445
CMM004 Common Variable Immunodeficiency 68 0.026
446
P MYS003 Myasthenia Gravis 68 0.026
447
P ESS003 Essential Thrombocythemia 68 0.026
448
P MJR001 Major Depressive Disorder 68 0.026
449
CHR103 Charge Syndrome 67 0.026
450
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.026
451
FCT007 Factor Vii Deficiency 67 0.026
452
P HYP098 Hypereosinophilic Syndrome 67 0.026
453
c ATS007 Autism Spectrum Disorder 67 0.026
454
GLL008 Gilles De La Tourette Syndrome 66 0.026
455
P DMN002 Dementia 66 0.026
456
P ATR011 Atrial Fibrillation 66 0.026
457
P DRM053 Dermatitis, Atopic 66 0.026
458
KHL003 Kohlschutter-Tonz Syndrome 65 0.026
459
P PLM036 Pulmonary Fibrosis 65 0.026
460
IRR002 Irritable Bowel Syndrome 65 0.026
461
P HRP006 Herpes Simplex 65 0.026
462
P PRS038 Personality Disorder 65 0.026
463
P ADL010 Adult Respiratory Distress Syndrome 65 0.026
464
PRT036 Peritonitis 64 0.026
465
MNK001 Menkes Disease 64 0.026
466
CLR108 Colorectal Adenoma 64 0.026
467
P FRD001 Friedreich Ataxia 64 0.026
468
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.026
469
P PRD008 Periodontitis 64 0.026
470
c CNG006 Congenital Hypothyroidism 64 0.026
471
P ADN016 Adenocarcinoma 64 0.026
472
KRN002 Kearns-Sayre Syndrome 63 0.026
473
P HML002 Hemolytic Anemia 63 0.026
474
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.026
475
P HYP069 Hyperparathyroidism 63 0.026
476
SKN016 Skin Disease 63 0.026
477
P SHR029 Short Syndrome 63 0.026
478
CHN016 Cohen Syndrome 63 0.026
479
TRN015 Transient Cerebral Ischemia 63 0.026
480
c ATM011 Autoimmune Hepatitis 63 0.026
481
c ALP101 Alpha-Thalassemia 62 0.026
482
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.026
483
HMT002 Hematologic Cancer 62 0.026
484
c FNC043 Fanconi Anemia, Complementation Group E 62 0.026
485
RTN209 Retinoschisis 1, X-Linked, Juvenile 62 0.026
486
P ART023 Arthropathy 62 0.026
487
P ORT004 Orthostatic Intolerance 62 0.026
488
INT002 Intermittent Claudication 61 0.026
489
CHR066 Chronic Fatigue Syndrome 61 0.026
490
WLD007 Waldenstroem's Macroglobulinemia 61 0.026
491
P PNC044 Pancreatitis 61 0.026
492
c PRT132 Protoporphyria, Erythropoietic, 1 61 0.026
493
PNM010 Pneumothorax, Primary Spontaneous 60 0.026
494
RGH009 Right Atrial Isomerism 60 0.026
495
DRR016 Diarrhea 2, with Microvillus Atrophy 60 0.026
496
P TST021 Testicular Germ Cell Tumor 60 0.026
497
FND001 Fundus Albipunctatus 60 0.026
498
c ACT027 Acute Pancreatitis 60 0.026
499
HPT019 Hepatic Encephalopathy 60 0.026
500
LNG099 Lung Disease 60 0.026
501
DNG002 Dengue Hemorrhagic Fever 60 0.026
502
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.026
503
VRC005 Varicose Veins 60 0.026
504
c ACT071 Acute Kidney Failure 60 0.026
505
P CHR285 Chronic Myelomonocytic Leukemia 60 0.026
506
P OPT006 Optic Nerve Disease 60 0.026
507
c HPT016 Hepatitis B 59 0.026
508
LKN001 Leukoencephalopathy with Vanishing White Matter 59 0.026
509
P SLP005 Sleep Disorder 59 0.026
510
c LTN004 Late-Onset Retinal Degeneration 59 0.026
511
P BRS044 Breast Adenocarcinoma 59 0.026
512
P DNG005 Dengue Virus 59 0.026
513
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.026
514
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.026
515
P PLY017 Polyarteritis Nodosa 58 0.026
516
P ANP001 Anaplastic Large Cell Lymphoma 58 0.026
517
P TYR004 Tyrosinemia 58 0.026
518
P HYP726 Hypercalcemia, Infantile, 1 58 0.026
519
ERY029 Erythermalgia, Primary 58 0.026
520
P PGT001 Paget's Disease of Bone 58 0.026
521
SCR008 Scrub Typhus 58 0.026
522
c PTT056 Pituitary Adenoma 1, Multiple Types 58 0.026
523
c PRM005 Primary Hyperparathyroidism 58 0.026
524
P MMP001 Mumps 58 0.026
525
LYM027 Lymphopenia 58 0.026
526
CHR081 Choroideremia 57 0.026
527
P INF032 Infertility 57 0.026
528
P GLM007 Glomerulonephritis 57 0.026
529
GLS018 Glass Syndrome 57 0.026
530
P OPT009 Optic Neuritis 57 0.026
531
CHL067 Cholecystitis 57 0.026
532
P EXN002 Exanthem 57 0.026
533
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.026
534
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.026
535
P END033 Endocarditis 57 0.026
536
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.026
537
P FTL001 Fetal Alcohol Syndrome 57 0.026
538
BLR008 Bilirubin Metabolic Disorder 57 0.026
539
SCH014 Schistosomiasis 57 0.026
540
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.026
541
INT303 Intracranial Hypertension, Idiopathic 57 0.026
542
P PYL005 Pyelonephritis 56 0.026
543
PNM008 Pneumothorax 56 0.026
544
c ACT134 Acute Liver Failure 56 0.026
545
LMY014 Leiomyoma, Uterine 56 0.026
546
c ESS001 Essential Tremor 56 0.026
547
BCT022 Bacterial Infectious Disease 56 0.026
548
GST050 Gastrointestinal System Disease 56 0.026
549
P LBR014 Leber Congenital Amaurosis 4 56 0.026
550
c GLY005 Glycogen Storage Disease Vi 56 0.026
551
P GST044 Gastritis 56 0.026
552
HYP005 Hypokalemia 55 0.026
553
LMB062 Limb Ischemia 55 0.026
554
P MLN007 Male Infertility 55 0.026
555
ANG005 Anogenital Venereal Wart 55 0.026
556
P MYP006 Myopia 55 0.026
557
ESN005 Eosinophilic Gastroenteritis 55 0.026
558
HRY003 Hairy Cell Leukemia 55 0.026
559
RSC001 Rosacea 54 0.026
560
PYD001 Pyoderma Gangrenosum 54 0.026
561
ACD008 Acid-Labile Subunit Deficiency 54 0.026
562
CRT017 Cartilage Disease 54 0.026
563
FCL014 Focal Epilepsy 54 0.026
564
PLM010 Pulmonary Edema 54 0.026
565
ANL018 Analbuminemia 54 0.026
566
HLL004 Hellp Syndrome 54 0.026
567
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.026
568
MYM001 Myoma 54 0.026
569
PNC001 Pancytopenia 54 0.026
570
MMM001 Mammary Paget's Disease 53 0.026
571
TRC023 Trichinosis 53 0.026
572
HYP801 Hyperferritinemia with or Without Cataract 53 0.026
573
P TCD001 Tic Disorder 53 0.026
574
CRY001 Cryptogenic Organizing Pneumonia 53 0.026
575
P EPD016 Epidermolysis Bullosa 53 0.026
576
RHM028 Rheumatic Heart Disease 53 0.026
577
GTR002 Goiter 53 0.026
578
HYP063 Hypersplenism 53 0.026
579
NRT001 Neurotic Disorder 53 0.026
580
GST023 Gastric Ulcer 53 0.026
581
P RTN022 Retinal Vein Occlusion 53 0.026
582
c HPT007 Hepatitis E 53 0.026
583
ALC009 Alcoholic Liver Cirrhosis 53 0.026
584
c PSR017 Psoriasis 2 53 0.026
585
P RTN018 Retinal Disease 53 0.026
586
CHR073 Choreatic Disease 52 0.026
587
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.026
588
c NGH026 Night Blindness, Congenital Stationary, Type 1a 52 0.026
589
c VRL010 Viral Hepatitis 52 0.026
590
ACR041 Acromelic Frontonasal Dysostosis 52 0.026
591
BTT001 Bietti Crystalline Corneoretinal Dystrophy 52 0.026
592
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.026
593
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.026
594
NRP045 Neuropathy, Ataxia, and Retinitis Pigmentosa 52 0.026
595
c PSR023 Psoriasis 1 52 0.026
596
BWN001 Bowen-Conradi Syndrome 52 0.026
597
PTH003 Pathologic Nystagmus 52 0.026
598
ACT200 Acute Monoblastic Leukemia 52 0.026
599
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.026
600
PRL019 Prolidase Deficiency 52 0.026
601
LMY002 Leiomyoma 52 0.026
602
SPS003 Spastic Diplegia 51 0.026
603
THR004 Thrombocytosis 51 0.026
604
RYS001 Reye Syndrome 51 0.026
605
c HYP602 Hyperoxaluria, Primary, Type Ii 51 0.026
606
KRT009 Keratosis 51 0.026
607
MLL018 Miller-Dieker Lissencephaly Syndrome 51 0.026
608
ENT011 Enterocolitis 51 0.026
609
ESP002 Esophageal Varix 51 0.026
610
P PRC012 Pericardial Effusion 51 0.026
611
P PST095 Post-Thrombotic Syndrome 51 0.026
612
P CHL066 Cholangitis 51 0.026
613
HYP081 Hypolipoproteinemia 51 0.026
614
CHR005 Chorioamnionitis 51 0.026
615
SCH012 Schizoaffective Disorder 50 0.026
616
PLR007 Pleural Empyema 50 0.026
617
PLR008 Pleurisy 50 0.026
618
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.026
619
P OVR082 Overgrowth Syndrome 50 0.026
620
RDC002 Radiculopathy 50 0.026
621
PST021 Postpartum Depression 50 0.026
622
HPT014 Hepatorenal Syndrome 50 0.026
623
c HYP603 Hyperoxaluria, Primary, Type Iii 50 0.026
624
BRN009 Burning Mouth Syndrome 50 0.026
625
c SVR005 Severe Pre-Eclampsia 50 0.026
626
P MTR003 Mitral Valve Stenosis 50 0.026
627
AZS001 Azoospermia 50 0.026
628
CRT013 Carotid Stenosis 50 0.026
629
c HRD202 Hereditary Lymphedema I 50 0.026
630
c INF145 Infantile Liver Failure Syndrome 1 50 0.026
631
PYD002 Pyoderma 50 0.026
632
P OBS001 Obstructive Jaundice 50 0.026
633
P OMP004 Omphalocele 50 0.026
634
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.026
635
WRN002 Wernicke-Korsakoff Syndrome 50 0.026
636
P ATR005 Atrophic Gastritis 50 0.026
637
c THR090 Thrombocythemia 1 49 0.026
638
ENT004 Enthesopathy 49 0.026
639
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.026
640
CRP032 Corpus Callosum, Agenesis of 49 0.026
641
MCR004 Macroglobulinemia 49 0.026
642
DDN006 Duodenitis 49 0.026
643
EPD006 Epidermolysis Bullosa Acquisita 49 0.026
644
P MGR001 Migraine Without Aura 49 0.026
645
P CMP008 Compartment Syndrome 49 0.026
646
c HPT015 Hepatitis D 49 0.026
647
RYN001 Raynaud Disease 48 0.026
648
INT017 Intestinal Schistosomiasis 48 0.026
649
P HYP058 Hypervitaminosis a 48 0.026
650
WTH001 Withdrawal Disorder 48 0.026
651
ASP007 Aspiration Pneumonia 48 0.026
652
P NGH001 Night Blindness 48 0.026
653
ACT098 Acute Erythroid Leukemia 48 0.026
654
VTM033 Vitamin K Deficiency Bleeding 48 0.026
655
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.026
656
SPL018 Splenomegaly 48 0.026
657
CHL056 Cheilitis 48 0.026
658
HMC041 Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity 48 0.026
659
TBR011 Tuberculous Meningitis 48 0.026
660
INT010 Intracranial Embolism 48 0.026
661
RCT020 Rectum Adenocarcinoma 48 0.026
662
PYL006 Pyloric Stenosis 48 0.026
663
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.026
664
HPR003 Heparin-Induced Thrombocytopenia 48 0.026
665
MLT006 Multidrug-Resistant Tuberculosis 48 0.026
666
SXL003 Sexual Disorder 47 0.026
667
CRD001 Cardiac Tamponade 47 0.026
668
CRN017 Coronary Thrombosis 47 0.026
669
c PSR032 Psoriasis 11 47 0.026
670
c OPT050 Opitz Gbbb Syndrome, Type Ii 47 0.026
671
GLS007 Glossitis 47 0.026
672
WRN003 Wernicke Encephalopathy 47 0.026
673
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.026
674
P RTN014 Retinal Artery Occlusion 47 0.026
675
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.026
676
TST044 Testicular Torsion 47 0.026
677
NSS002 Neisseria Meningitidis Infection 47 0.026
678
RYN005 Raynaud Phenomenon 47 0.026
679
HYP034 Hypertensive Encephalopathy 46 0.026
680
BCK003 Background Diabetic Retinopathy 46 0.026
681
ORC001 Orchitis 46 0.026
682
MDS022 Mediastinitis 46 0.026
683
MNN020 Meningococcal Infection 46 0.026
684
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.026
685
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.026
686
VGN019 Vaginal Discharge 46 0.026
687
ANR004 Anuria 46 0.026
688
c ACT042 Acute Pyelonephritis 46 0.026
689
EPD015 Epidemic Typhus 45 0.026
690
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.026
691
SYN036 Syncope 45 0.026
692
GLC022 Glucose/galactose Malabsorption 45 0.026
693
c TRC022 Tricuspid Valve Insufficiency 45 0.026
694
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.026
695
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.026
696
HPT004 Hepatic Coma 45 0.026
697
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.026
698
PRL008 Paralytic Ileus 45 0.026
699
P OCY003 Oocyte Maturation Defect 1 45 0.026
701
c HMP012 Hemophagocytic Lymphohistiocytosis, Familial, 2 45 0.026
702
c ZLL011 Zellweger Spectrum Disorder 45 0.026
703
MYF001 Myofibroma 45 0.026
704
SPS057 Spasticity 45 0.026
705
P FTL033 Fetal Hemoglobin Quantitative Trait Locus 1 45 0.026
706
ASP026 Asplenia, Isolated Congenital 44 0.026
707
P TRC087 Tricuspid Valve Disease 44 0.026
708
ISC015 Ischemic Colitis 44 0.026
709
c SPR086 Spermatogenic Failure 3 44 0.026
710
MCR017 Macrocytic Anemia 44 0.026
711
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.026
712
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.026
713
MND023 Mend Syndrome 43 0.026
714
MYX004 Myxedema 43 0.026
715
IDP073 Idiopathic Hypercalciuria 43 0.026
716
ORL015 Oral Squamous Cell Carcinoma 43 0.026
717
HMP009 Haemophilus Influenzae 43 0.026
718
DRG002 Drug-Induced Hepatitis 43 0.026
719
TRP009 Triple X Syndrome 42 0.026
720
c RTN047 Retinitis Pigmentosa 18 42 0.026
721
P VND001 Vein Disease 42 0.026
722
c PSR028 Psoriasis 7 42 0.026
723
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.026
724
DRG024 Drug Allergy 42 0.026
725
P HYP441 Hyperphosphatasia with Mental Retardation Syndrome 1 42 0.026
726
ATX019 Ataxia with Vitamin E Deficiency 42 0.026
727
FSC002 Fascioliasis 42 0.026
728
GLT005 Glutamate Formiminotransferase Deficiency 41 0.026
729
GST020 Gastric Antral Vascular Ectasia 41 0.026
730
49X006 49, Xxxxy Syndrome 41 0.026
731
LYM010 Lymph Node Tuberculosis 41 0.026
732
c PSR018 Psoriasis 13 41 0.026
733
P CRB045 Cerebellar Hypoplasia 41 0.026
734
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.026
735
RDN001 Reading Disorder 40 0.026
736
ANX004 Anoxia 40 0.026
737
HPR006 Heparin Cofactor Ii Deficiency 40 0.026
738
PYR004 Pyuria 40 0.026
739
P PRG092 Pregnancy Loss, Recurrent 1 40 0.026
740
RFL002 Reflex Epilepsy 40 0.026
741
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 40 0.026
742
LNG030 Lung Adenoma 39 0.026
743
P DYS021 Dysautonomia 39 0.026
744
LKP003 Leukoplakia 39 0.026
745
RCK002 Rocky Mountain Spotted Fever 39 0.026
746
HYP344 Hyperthyroidism, Familial Gestational 39 0.026
747
CHL070 Cholesterol Embolism 39 0.026
748
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.026
749
NRD004 Neurodegeneration Due to Cerebral Folate Transport Deficiency 39 0.026
750
ESN002 Eosinophilia-Myalgia Syndrome 38 0.026
751
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.026
752
ABD004 Abdominal Tuberculosis 38 0.026
753
SPL006 Splenic Infarction 38 0.026
754
CHL039 Choledocholithiasis 38 0.026
755
P PRC031 Preeclampsia/eclampsia 1 38 0.026
756
HYP264 Hypertonia 38 0.026
757
MLN003 Melancholia 38 0.026
758
CHL073 Cholestasis-Lymphedema Syndrome 38 0.026
759
VSM001 Vasomotor Rhinitis 38 0.026
760
MCP033 Mucopolysaccharidoses 38 0.026
761
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 38 0.026
762
CRB009 Cerebritis 37 0.026
763
ORL019 Oral Hairy Leukoplakia 37 0.026
764
ASP024 Asparagine Synthetase Deficiency 37 0.026
765
MYC017 Mycobacterium Kansasii 36 0.026
766
c HMG004 Hemoglobin D Disease 36 0.026
767
ABD010 Abdominal Wall Defect 36 0.026
768
MLD002 Mild Pre-Eclampsia 36 0.026
769
P AXN001 Axonal Neuropathy 36 0.026
770
HRW001 Hair Whorl 36 0.026
771
LVD003 Livedoid Vasculitis 36 0.026
772
c ACT036 Acute Cholangitis 36 0.026
773
ACL001 Acalculous Cholecystitis 35 0.026
774
PRM329 Premature Aging 35 0.026
775
END072 Endotheliitis 35 0.026
776
PCT001 Pectus Carinatum 35 0.026
777
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.026
778
CHR034 Chromophobe Adenoma 34 0.026
779
P HPT020 Hepatic Vascular Disease 34 0.026
780
HNS001 Hansen's Disease 34 0.026
781
GRM010 Germ Cells Tumors 34 0.026
782
FCL090 Facial Cleft 34 0.026
784
MTH086 Methotrexate Toxicity 33 0.026
785
c PRS136 Prostate Cancer, Hereditary, 6 33 0.026
786
HPT081 Hepatic Infarction 33 0.026
787
ART110 Arteritic Anterior Ischemic Optic Neuropathy 33 0.026
788
HPT008 Hepatic Tuberculosis 32 0.026
789
c PRS130 Prostate Cancer, Hereditary, 8 32 0.026
790
SGT001 Sagittal Sinus Thrombosis 32 0.026
791
SLW005 Slowed Nerve Conduction Velocity, Autosomal Dominant 32 0.026
792
c CLR079 Colorectal Cancer 2 32 0.026
793
CCL002 Cecal Disease 31 0.026
794
RFR009 Refractory Cytopenia with Multilineage Dysplasia 31 0.026
795
c ALC016 Alcohol Sensitivity, Acute 31 0.026
796
EMP002 Emphysematous Cholecystitis 30 0.026
797
ISL119 Isolated Optic Neuritis 30 0.026
798
FNT004 Fainting 30 0.026
799
CLF051 Cleft Larynx, Posterior 30 0.026
800
MTY003 Mutyh Polyposis 30 0.026
801
ACT228 Acute Radiation Syndrome 29 0.026
802
P PRC050 Pericardium Disease 29 0.026
803
ASC003 Ascending Cholangitis 29 0.026
804
TMP019 Temporomandibular Joint Anomaly 28 0.026
805
THY039 Thyrotropin-Releasing Hormone Deficiency 28 0.026
806
SPL007 Splenic Abscess 28 0.026
807
URG001 Urogenital Tuberculosis 28 0.026
808
PYL002 Pylorospasm 27 0.026
809
c CMM007 Common Bile Duct Disease 27 0.026
810
PRT025 Protein-Deficiency Anemia 27 0.026
811
CYT018 Cytochrome P450 2d6 Variant 27 0.026
812
LRY026 Laryngeal Cleft 27 0.026
813
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.026
814
MLR020 Malaria, Mild 27 0.026
815
ANG061 Angular Cheilitis 26 0.026
816
GMM004 Gamma-Amino Butyric Acid Metabolism Disorder 26 0.026
817
MDN002 Median Neuropathy 26 0.026
818
ETH012 Ethylene Glycol Poisoning 26 0.026
819
PRQ002 Paraquat Poisoning 26 0.026
820
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.026
821
NRM022 Neurometabolic Disease 25 0.026
822
PRN071 Parenteral Nutrition-Associated Cholestasis 25 0.026
823
c PNM004 Pneumoconiosis Due to Talc 24 0.026
825
P PHC014 Phocomelia 24 0.026
826
GNT018 Gianotti Crosti Syndrome 23 0.026
827
HPT066 Hepatoportal Sclerosis 23 0.026
828
c ANK021 Ankylosing Spondylitis 1 23 0.026
829
CHR158 Charles Bonnet Syndrome 23 0.026
830
c CLR082 Colorectal Cancer 7 22 0.026
831
PNC007 Pancreas Lymphoma 18 0.026
832
CRB089 Cerebral Beriberi 18 0.026
833
LNR001 Leiner Disease 17 0.026
834
UNC008 Unclassified Myelodysplastic Syndrome 14 0.026
835
CNV019 Convulsive Disorder, Familial, with Prenatal or Early Onset 9 0.026
Content
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