The MalaCard for "alcoholism" has been retired.
Searching MalaCards for entries containing "alcoholism"

1333 hits were found for 'alcoholism'

# ++ Fam MCID Name MIFTS Score
1
P FTL006 Fetal Alcohol Spectrum Disorder 51 7.414
2
ALC006 Alcoholic Hepatitis 52 5.674
3
ALC009 Alcoholic Liver Cirrhosis 52 5.667
4
ALC007 Alcohol Dependence 59 5.463
5
ALC011 Alcoholic Neuropathy 28 4.707
6
ALC005 Alcoholic Pancreatitis 44 4.437
7
P ALC004 Alcohol Abuse 55 4.423
8
ALC003 Alcoholic Psychosis 28 4.240
9
ALC010 Alcoholic Cardiomyopathy 44 4.209
10
ALC012 Alcoholic Gastritis 10 3.860
11
c FTL001 Fetal Alcohol Syndrome 44 3.842
12
FTT001 Fatty Liver Disease 58 3.708
13
NNL002 Nonalcoholic Steatohepatitis 50 3.159
14
WRN002 Wernicke-Korsakoff Syndrome 50 3.110
15
PRT001 Partial Fetal Alcohol Syndrome 21 3.038
16
ALC002 Alcohol-Related Neurodevelopmental Disorder 25 3.032
17
ALC001 Alcohol-Related Birth Defect 25 3.022
18
ACT189 Acute Neonatal Citrullinemia Type I 12 2.614
19
ALC017 Alcohol Dependence, Protection Against 12 2.482
20
MYC011 Myoclonus-Dystonia 51 2.439
21
c ALC016 Alcohol Sensitivity, Acute 6 2.419
22
ALC013 Alcohol-Induced Mental Disorder 4 2.419
23
ARD004 Aerodigestive Tract Cancer, Squamous Cell, Alcohol-Related, Protection Against 3 2.407
24
ESP042 Esophageal Cancer, Alcohol-Related 3 2.407
25
DMN026 Dementia Pugilistica 17 1.893
26
P DYS098 Dystonia-11, Myoclonic 22 1.767
27
P SJG002 Sjogren-Larsson Syndrome 47 1.702
28
P LVR013 Liver Disease 62 0.575
29
c HPT021 Hepatitis 65 0.500
30
c HPT003 Hepatitis a 57 0.498
31
c PNC044 Pancreatitis 58 0.377
32
P HPT001 Hepatitis C 66 0.358
33
LVR012 Liver Cirrhosis 69 0.352
34
P PNC102 Pancreatitis, Chronic 41 0.258
35
c HPT015 Hepatitis D 59 0.256
36
DRG003 Drug Dependence 50 0.237
37
NSY001 N Syndrome 57 0.221
38
c XP2001 Xp22.3 Microdeletion Syndrome 17 0.213
39
c HPT007 Hepatitis E 52 0.207
40
HNG003 Hangover 34 0.204
41
END072 Endotheliitis 51 0.198
42
P INS005 Insulin Resistance 62 0.188
43
c ACT027 Acute Pancreatitis 60 0.168
44
14Q004 14q22q23 Microdeletion Syndrome 25 0.166
45
IDP042 Idiopathic Recurrent Stupor 15 0.166
46
3Q2005 3q26q27 Microdeletion Syndrome 14 0.166
47
c HPT016 Hepatitis B 62 0.165
48
DRG011 Drug Addiction 53 0.165
49
NRP001 Neuropathy 54 0.162
50
P PRS038 Personality Disorder 56 0.157
51
HPT023 Hepatocellular Carcinoma 69 0.156
52
CCN001 Cocaine Dependence 54 0.150
53
NCT002 Nicotine Dependence 49 0.146
54
SBS003 Substance Abuse 55 0.141
55
P BRS047 Breast Cancer 85 0.137
56
P BPL003 Bipolar Disorder 76 0.137
57
SQM006 Squamous Cell Carcinoma 58 0.137
58
ANT011 Antisocial Personality Disorder 55 0.137
59
CYT018 Cytochrome P450 2d6 Variant 12 0.137
60
P OBS005 Obesity 79 0.133
61
P SCH015 Schizophrenia 69 0.130
62
GLL008 Gilles De La Tourette Syndrome 60 0.128
63
GNR028 Generalized Essential Telangiectasia 16 0.128
64
P HYP075 Hypertension 76 0.124
65
ANX002 Anxiety Disorder 73 0.124
66
CND002 Conduct Disorder 56 0.124
67
21Q001 21q22.11q22.12 Microdeletion Syndrome 13 0.122
68
ESP021 Esophageal Cancer 68 0.121
69
SPS077 Sepsis 67 0.121
70
SDR002 Siderosis 50 0.121
71
ATX002 Ataxia Telangiectasia 81 0.119
72
c ERL020 Early-Onset Schizophrenia 44 0.119
73
c HPT073 Hepatitis C Virus 43 0.119
74
ANK002 Ankylosing Spondylitis 75 0.117
75
TFT003 Tufting Enteropathy 26 0.117
76
P CLR023 Colorectal Cancer 66 0.116
77
THR013 Thoracic Outlet Syndrome 53 0.114
78
SBS004 Substance Dependence 49 0.114
79
c VRL010 Viral Hepatitis 57 0.112
80
CCN002 Cocaine Abuse 52 0.112
81
P PNC025 Panic Disorder 62 0.110
82
ALX002 Alexithymia 43 0.109
83
14Q001 14q12 Microdeletion Syndrome 23 0.109
84
c 2P1003 2p13.2 Microdeletion Syndrome 11 0.109
85
ORL011 Oral Cancer 50 0.107
86
LDP002 Lead Poisoning 47 0.107
87
MLR006 Male Reproductive Organ Cancer 21 0.105
88
c DST058 Distal Monosomy 12p 16 0.105
89
MNS013 Monosomy 13q34 14 0.105
90
c DBT009 Diabetes Mellitus 68 0.103
91
LPT005 Leptin Deficiency 40 0.103
92
P CRN157 Coronary Heart Disease 59 0.101
93
PTH002 Pathological Gambling 55 0.101
94
ADN064 Adenohypophysitis 42 0.101
95
SRC015 Sarcosinemia 34 0.101
96
17Q001 17q21.31 Microdeletion Syndrome 29 0.101
97
c CHR226 Chromosome 1q41-Q42 Deletion Syndrome 23 0.101
98
MCR071 Microdeletion 15q11.2 21 0.101
99
BRN029 Brain Disease 60 0.099
100
TBR011 Tuberculous Meningitis 51 0.099
101
SDD005 Sudden Cardiac Death Multi-Gene Panels 19 0.099
102
MMR004 Memory Impairment 52 0.097
103
CNT025 Central Pontine Myelinolysis 40 0.095
104
ATH003 Atherosclerosis 69 0.093
105
CRB088 Cerebral Atrophy 46 0.093
106
CNN001 Cannabis Dependence 37 0.093
107
c 2Q3005 2q31.1 Microdeletion Syndrome 22 0.093
108
17Q007 17q11 Microdeletion Syndrome 21 0.093
109
c HYP061 Hypertrophic Cardiomyopathy 59 0.091
110
SCN006 Secondary Syphilis 53 0.091
111
c ERL004 Early Yaws 29 0.091
112
ATT002 Attention Deficit Hyperactivity Disorder 72 0.089
113
CHR101 Char Syndrome 42 0.089
114
PRL042 Proliferating Trichilemmal Cyst 40 0.089
115
P PRK002 Parkinson's Disease 86 0.086
116
BRN024 Bronchitis 71 0.086
117
P HYP117 Hypertriglyceridemia 63 0.086
118
c PRP029 Porphyria 56 0.086
119
IDP044 Idiopathic Pulmonary Alveolar Proteinosis 47 0.086
120
ACN002 Acanthosis Nigricans 70 0.084
121
WST001 West Syndrome 64 0.084
122
MDD011 Mood Disorder 56 0.084
123
OPT003 Opiate Dependence 51 0.084
124
JCB001 Jacobsen Syndrome 49 0.084
125
WRN003 Wernicke Encephalopathy 41 0.084
126
CHL079 Children's Interstitial Lung Disease 39 0.084
127
ESP028 Esophageal Squamous Cell Carcinoma 39 0.084
128
NNT020 Neonatal Intrahepatic Cholestasis Caused by Citrin Deficiency 33 0.084
129
FLM003 Fulminant Viral Hepatitis 30 0.084
130
NNS006 Non-Suppurative Otitis Media 24 0.084
131
LPD027 Lip Disease 23 0.084
132
19Q001 19q13.11 Microdeletion Syndrome 21 0.084
133
PSY004 Psychotic Disorder 62 0.082
134
LNG032 Lung Cancer 61 0.082
135
P ADN016 Adenocarcinoma 60 0.082
136
P GST044 Gastritis 59 0.082
137
HRD057 Hereditary Pancreatitis 53 0.082
138
ADL002 Adult Syndrome 50 0.082
139
P LRY035 Laryngo-Tracheo-Esophageal Cleft 17 0.082
140
ADN018 Adenoma 67 0.079
141
PRT036 Peritonitis 67 0.079
142
BRN071 Brain Injury 57 0.079
143
EXT034 Extrinsic Allergic Alveolitis 55 0.079
144
PDT035 Pediatric Systemic Lupus Erythematosus 40 0.079
145
WRF001 Warfarin Resistance 33 0.079
146
c CHR266 Chromosome 8p23.1 Deletion 21 0.079
147
MRC001 Marchiafava Bignami Disease 21 0.079
148
P ALZ001 Alzheimer's Disease 93 0.077
149
c LCL006 Localized Scleroderma 64 0.077
150
P STM004 Stomach Cancer 62 0.077
151
P DMN002 Dementia 61 0.077
152
EVN001 Evans' Syndrome 50 0.077
153
P PLL002 Pellagra 48 0.077
154
WTH001 Withdrawal Disorder 40 0.077
155
c CRB059 Cerebellar Degeneration 36 0.077
156
c RNG028 Ring Chromosome Y 17 0.077
157
P PNC035 Pancreatic Cancer 82 0.074
158
P ANR007 Anorexia Nervosa 64 0.074
159
DRM006 Dermatitis 60 0.074
160
c BLN003 Blindness 54 0.074
161
SCL003 Social Phobia 54 0.074
162
PSR002 Psoriasis 51 0.074
163
HYP459 Hyperferritinemia Cataract Syndrome 44 0.074
164
c INT099 Intrahepatic Cholestasis of Pregnancy 37 0.074
165
EPS023 Epstein-Barr Virus-Associated Gastric Carcinoma 35 0.074
166
17Q004 17q12 Microdeletion Syndrome 32 0.074
167
BNZ002 Benzene Toxicity 28 0.074
168
P DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 23 0.074
169
AFF001 Afferent Loop Syndrome 19 0.074
170
P LNG072 Lung Cancer Susceptibility 2 16 0.074
171
VRS002 Virus-Associated Trichodysplasia Spinulosa 10 0.074
172
FNC001 Fanconi's Anemia 66 0.071
173
TRM010 Traumatic Brain Injury 54 0.071
174
c CHR345 Chronic Pain 53 0.071
175
c TRM003 Tremor 50 0.071
176
HPT014 Hepatorenal Syndrome 49 0.071
177
NCT012 Nicotine Addiction 48 0.071
178
STR077 Streptococcal Toxic-Shock Syndrome 42 0.071
179
c BPL002 Bipolar I Disorder 41 0.071
180
MYC019 Mycobacterium Marinum 37 0.071
181
PYR016 Pyridoxine Deficiency 33 0.071
182
ACT181 Acute Motor Axonal Neuropathy 19 0.071
183
P PRT013 Portal Hypertension 65 0.069
184
PST028 Post-Traumatic Stress Disorder 61 0.069
185
HMR012 Hemorrhagic Fever 58 0.069
186
DWN001 Down Syndrome 58 0.069
187
P MJR001 Major Depressive Disorder 58 0.069
188
SRT004 Serotonin Syndrome 53 0.069
189
HPT019 Hepatic Encephalopathy 51 0.069
190
NTR021 Nutrition Disease 48 0.069
191
CRB009 Cerebritis 46 0.069
192
c ACR001 Aicardi-Goutieres Syndrome 46 0.069
193
P HRM005 Hermansky-Pudlak Syndrome 1 44 0.069
194
1P3001 1p36 Deletion Syndrome 44 0.069
195
P HYP090 Hyperalphalipoproteinemia 43 0.069
196
CHL039 Choledocholithiasis 40 0.069
197
VTM002 Vitamin B12 Deficiency 35 0.069
198
FCT013 Factor V Leiden Thrombophilia 31 0.069
199
DFN039 Deafness-Infertility Syndrome 24 0.069
200
c TTL001 Total Internal Ophthalmoplegia 17 0.069
201
10P002 10p11.21p12.31 Microdeletion Syndrome 14 0.069
202
12Q001 12q15q21.1 Microdeletion Syndrome 14 0.069
203
P MYC007 Myocardial Infarction 82 0.066
204
P PRP003 Porphyria Cutanea Tarda 68 0.066
205
P PNM007 Pneumonia 67 0.066
206
CRB011 Cerebrotendinous Xanthomatosis 66 0.066
207
IRN001 Iron Deficiency Anemia 58 0.066
208
c ACT134 Acute Liver Failure 55 0.066
209
P XNT003 Xanthomatosis 54 0.066
210
c MYP004 Myopathy 52 0.066
211
HRN003 Heroin Dependence 50 0.066
212
c INS004 Insomnia 47 0.066
213
AMB002 Amblyopia 46 0.066
214
PRP023 Peripheral Neuropathy 46 0.066
215
YNG002 Young Syndrome 34 0.066
216
MDL006 Madelung Disease 28 0.066
217
DMN016 Dementia, Familial, Nonspecific 26 0.066
218
12P001 12p12.1 Microdeletion Syndrome 15 0.066
219
FBR065 Fibrocalculous Pancreatopathy 14 0.066
220
TBR010 Tuberculosis 82 0.063
221
WLS001 Wilson Disease 74 0.063
222
RLP001 Relapsing Polychondritis 66 0.063
223
c ESS002 Essential Hypertension 64 0.063
224
CRM001 Crimean-Congo Hemorrhagic Fever 58 0.063
225
MYC002 Mycobacterium Avium Complex Disease 56 0.063
226
HYP037 Hyperhomocysteinemia 55 0.063
227
GNR004 Generalized Anxiety Disorder 53 0.063
228
PRM126 Primary Peritoneal Carcinoma 51 0.063
229
P ESP024 Esophagitis 51 0.063
230
LKM001 Leukemoid Reaction 44 0.063
231
RCR001 Recurrent Corneal Erosion 43 0.063
232
RHM014 Rheumatoid Vasculitis 41 0.063
233
MLT012 Multiple Symmetric Lipomatosis 41 0.063
234
c 3Q2003 3q29 Microdeletion Syndrome 37 0.063
235
BRG002 Berger Disease 30 0.063
236
c CNG224 Congenital Disorder of Glycosylation Type 1a 28 0.063
237
CRK001 Cork-Handlers' Disease 28 0.063
238
12Q002 12q14 Microdeletion Syndrome 28 0.063
239
ADL082 Adult Pulmonary Langerhans Cell Histiocytosis 26 0.063
240
2Q3003 2q32q33 Microdeletion Syndrome 25 0.063
241
c 2Q2001 2q23.1 Microdeletion Syndrome 25 0.063
242
c 4Q2001 4q21 Microdeletion Syndrome 24 0.063
243
P STR035 Streptococcal Group a Invasive Disease 15 0.063
244
SDD004 Sudden Arrhythmia Death Syndrome 15 0.063
245
P HMC003 Hemochromatosis 73 0.059
246
PCK001 Pick's Disease 68 0.059
247
CRZ001 Crouzon Syndrome 67 0.059
248
ACQ007 Acquired Immunodeficiency Syndrome 62 0.059
249
HDC001 Headache 58 0.059
250
BNN001 Bannayan-Riley-Ruvalcaba Syndrome 57 0.059
251
ETN001 Eating Disorder 55 0.059
252
CHL068 Cholestasis 55 0.059
253
SCH012 Schizoaffective Disorder 54 0.059
254
ART001 Arterial Tortuosity Syndrome 52 0.059
255
CNG048 Congenital Hepatic Fibrosis 52 0.059
256
MLT006 Multidrug-Resistant Tuberculosis 51 0.059
257
LPM004 Lipoma 51 0.059
258
P PND001 Pain Disorder 49 0.059
259
CNT047 Contact Dermatitis 49 0.059
260
PRM003 Premature Ejaculation 48 0.059
261
MYC033 Myoclonus 47 0.059
262
LPM005 Lipomatosis 45 0.059
263
P MBS002 Moebius Syndrome 45 0.059
264
AND003 Andersen-Tawil Syndrome 39 0.059
265
c ATX010 Ataxia Neuropathy Spectrum 33 0.059
266
GRD005 Geroderma Osteodysplasticum 31 0.059
267
P SLP004 Salpingo-Oophoritis 30 0.059
268
CNG034 Congestive Heart Failure 74 0.056
269
CLN016 Colon Cancer 66 0.056
270
21H001 21-Hydroxylase Deficiency 62 0.056
271
c MNN013 Meningitis 62 0.056
272
GLC003 Glucose Intolerance 62 0.056
273
LRY016 Laryngeal Carcinoma 58 0.056
274
NRL004 Neuroleptic Malignant Syndrome 53 0.056
275
SSN001 Seasonal Affective Disorder 51 0.056
276
ORL007 Oral Cavity Cancer 50 0.056
277
PNM013 Pneumococcal Meningitis 47 0.056
278
LKP003 Leukoplakia 45 0.056
279
AGR002 Agoraphobia 45 0.056
280
AMN003 Amnestic Disorder 35 0.056
281
CNN002 Cannabis Abuse 33 0.056
282
NRT005 North Carolina Macular Dystrophy 31 0.056
283
MNT053 Mental Retardation, Stereotypic Movements, Epilepsy, and/or Cerebral Malformations 29 0.056
284
HVD003 Hiv/aids 27 0.056
285
c CNG372 Congenital Generalized Lipodystrophy Type 3 24 0.056
286
CNG101 Congenital Human Immunodeficiency Virus 24 0.056
287
PNC059 Punctate Inner Choroidopathy 20 0.056
288
PRT015 Partial Third-Nerve Palsy 19 0.056
289
c 9P1001 9p13 Microdeletion Syndrome 13 0.056
290
c 5Q3002 5q31.3 Microdeletion Syndrome 13 0.056
291
AND002 Androgen Insensitivity Syndrome 75 0.052
292
GLC006 Galactosemia 74 0.052
293
OBS002 Obsessive-Compulsive Disorder 71 0.052
294
CRN211 Coronary Artery Disease, 68 0.052
295
P ANG001 Angelman Syndrome 67 0.052
296
ART019 Aortic Valve Stenosis 64 0.052
297
SPT013 Septic Shock 62 0.052
298
LCH002 Lichen Planus 61 0.052
299
BRN106 Burns 61 0.052
300
P CLF002 Cleft Palate 60 0.052
301
P ESS001 Essential Tremor 59 0.052
302
MLT074 Multiple Endocrine Neoplasia 58 0.052
303
P CNV004 Canavan Disease 58 0.052
304
c AXN002 Axenfeld-Rieger Syndrome 57 0.052
305
P INF032 Infertility 55 0.052
306
PST046 Post-Transplant Lymphoproliferative Disease 54 0.052
307
ALL010 Allergic Contact Dermatitis 52 0.052
308
NRM004 Neuroma 48 0.052
309
SCH018 Schizencephaly 47 0.052
310
LKS001 Leukostasis 45 0.052
311
HPT032 Hepatocellular Carcinoma, Somatic 43 0.052
312
LPT006 Leptin Receptor Deficiency 43 0.052
313
EGG001 Egg Allergy 43 0.052
314
LNG017 Lung Giant Cell Carcinoma 43 0.052
315
ORL012 Oral Leukoplakia 42 0.052
316
ORL015 Oral Squamous Cell Carcinoma 40 0.052
317
MNN014 Mononeuritis 40 0.052
318
BRB001 Beriberi 40 0.052
319
c MYP006 Myopia 36 0.052
320
P INT072 Intestinal Pseudo-Obstruction 35 0.052
321
P EPL025 Epileptic Encephalopathy, Early Infantile, 2 35 0.052
322
GNT019 Giant Cell Myocarditis 33 0.052
323
OPD001 Opioid Abuse 32 0.052
324
c AMY006 Amyotrophic Lateral Sclerosis with Frontotemporal Dementia 32 0.052
325
TRP008 Tropical Calcific Pancreatitis 30 0.052
326
P EHL043 Ehlers-Danlos Syndrome, Progeroid Type, 1 30 0.052
327
PRQ002 Paraquat Poisoning 29 0.052
328
DSS011 Dissecting Cellulitis of the Scalp 26 0.052
329
c BNG076 Benign Exophthalmos Syndrome 17 0.052
330
P ISC010 Isochromosome Yp 14 0.052
331
CYS001 Cystic Fibrosis 91 0.049
332
P MLT020 Multiple Sclerosis 75 0.049
333
P OST002 Osteoporosis 73 0.049
334
P PRD006 Prader-Willi Syndrome 69 0.049
335
P PRM006 Primary Biliary Cirrhosis 69 0.049
336
P ADL010 Adult Respiratory Distress Syndrome 66 0.049
337
HYP056 Hypoglycemia 66 0.049
338
GST034 Gastroesophageal Reflux Disease 65 0.049
339
P SDD001 Sudden Infant Death Syndrome 65 0.049
340
P DDN001 Duodenal Ulcer 63 0.049
341
CHL065 Cholangiocarcinoma 61 0.049
342
MRB003 Morbid Obesity 60 0.049
343
LWY001 Lewy Body Dementia 60 0.049
344
SCH014 Schistosomiasis 59 0.049
345
PRN009 Paranoid Schizophrenia 57 0.049
346
APH001 Aphthous Stomatitis 56 0.049
347
ADR005 Adrenal Carcinoma 56 0.049
348
c EMR001 Emery-Dreifuss Muscular Dystrophy 56 0.049
349
PPT003 Peptic Ulcer 55 0.049
350
CMM005 Common Cold 55 0.049
351
THY089 Thymic Epithelial Neoplasm 53 0.049
352
c KDN018 Kidney Disease 52 0.049
353
HYP017 Hypophosphatemia 52 0.049
354
DBT004 Diabetic Polyneuropathy 52 0.049
355
BRD004 Borderline Personality Disorder 52 0.049
356
LFT009 Left Ventricular Outflow Tract Obstruction 52 0.049
357
GNR017 Generalized Pustular Psoriasis 51 0.049
358
HMS001 Hemosiderosis 51 0.049
359
P CHL066 Cholangitis 50 0.049
360
P CLC001 Calciphylaxis 49 0.049
361
P ATR005 Atrophic Gastritis 48 0.049
362
INV001 Invasive Aspergillosis 47 0.049
363
P HYP141 Hyperphenylalaninemia 47 0.049
364
CMB021 Combined Pituitary Hormone Deficiency 46 0.049
365
STN007 Stenotrophomonas Maltophilia 46 0.049
366
LMB052 Lumbar Disc Herniation 46 0.049
367
c BNG049 Benign Recurrent Intrahepatic Cholestasis 45 0.049
368
TXC002 Toxic Encephalopathy 45 0.049
369
PRT038 Protein-Energy Malnutrition 45 0.049
370
HYP121 Hypoalphalipoproteinemia 44 0.049
371
IRN002 Iron Metabolism Disease 44 0.049
372
IDP035 Idiopathic Achalasia 43 0.049
373
HV1006 Hiv-1 42 0.049
374
INT103 Intrauterine Infections 41 0.049
375
ATX019 Ataxia with Vitamin E Deficiency 40 0.049
376
ENT001 Enterocele 39 0.049
377
HPT025 Hepatic Lipase Deficiency 38 0.049
378
c CHR455 Chiari Malformations 38 0.049
379
c RCR022 Recurrent Acute Pancreatitis 35 0.049
380
EMN001 Emanuel Syndrome 34 0.049
381
c ATM029 Autoimmune Lymphoproliferative Syndrome, Type Ib 33 0.049
382
MSM007 Mesomelic Dysplasia Kantaputra Type 32 0.049
383
15Q001 15q13.3 Microdeletion 29 0.049
384
JVN024 Juvenile Hereditary Hemochromatosis 28 0.049
385
APD001 Apo a-I Deficiency 26 0.049
386
MTH047 Methanol Poisoning 26 0.049
387
16Q001 16q24.3 Microdeletion Syndrome 23 0.049
388
DPN001 Dependent Personality Disorder 22 0.049
389
GRF006 Grfoma 20 0.049
390
BRB003 Barbiturate Abuse 10 0.049
391
P AST005 Asthma 86 0.044
392
P TYP009 Type 2 Diabetes Mellitus 80 0.044
393
P PRS040 Prostate Cancer 76 0.044
394
LKM002 Leukemia 70 0.044
395
P UVT001 Uveitis 66 0.044
396
IRR002 Irritable Bowel Syndrome 65 0.044
397
P MLT021 Multiple System Atrophy 64 0.044
398
PRP030 Purpura 60 0.044
399
P GLM007 Glomerulonephritis 60 0.044
400
CRY002 Cryptorchidism 59 0.044
401
HYP014 Hyperuricemia 58 0.044
402
BLM002 Bulimia Nervosa 58 0.044
403
P PRD008 Periodontitis 58 0.044
404
ISC004 Ischemia 57 0.044
405
VNS009 Venous Thrombosis 56 0.044
406
P RST001 Restless Legs Syndrome 56 0.044
407
CRC006 Carcinoid Syndrome 55 0.044
408
c SBC007 Subacute Thyroiditis 55 0.044
409
BNF002 Bone Fracture 53 0.044
410
P CLL015 Collagen Disease 52 0.044
411
HPY002 H. Pylori Infection 52 0.044
412
HYP063 Hypersplenism 52 0.044
413
FBR047 Fibromyalgia 52 0.044
414
SMT019 Somatostatin Analog 51 0.044
415
OBS001 Obstructive Jaundice 50 0.044
416
SPL018 Splenomegaly 50 0.044
417
c INT001 Intrahepatic Cholestasis 50 0.044
418
OST003 Osteonecrosis 49 0.044
419
MST002 Mast-Cell Leukemia 47 0.044
420
PYM001 Pyomyositis 44 0.044
421
FSC004 Fasciitis 44 0.044
422
PLR009 Pol Iii-Related Leukodystrophies 42 0.044
423
INT063 Intellectual Disability 42 0.044
424
CRD053 Cardiovascular Disease Risk Factor 42 0.044
425
CRY001 Cryptogenic Organizing Pneumonia 41 0.044
426
SCH003 Schizophreniform Disorder 39 0.044
427
DLS001 Delusional Disorder 38 0.044
428
OPT037 Optic Nerve Hypoplasia 37 0.044
429
STR037 Stress Cardiomyopathy 37 0.044
430
P CLR019 Color Blindness 36 0.044
431
OBS003 Obsessive-Compulsive Personality Disorder 33 0.044
432
CTR003 Citrin Deficiency 32 0.044
433
MYC020 Mycobacterium Tuberculosis, Susceptibility to Infection by 32 0.044
434
HNM001 Hinman's Syndrome 28 0.044
435
ADG002 Audiogenic Seizures 28 0.044
436
BRT037 Brittle Diabetes 27 0.044
437
VST004 Vestibular Disease 26 0.044
438
FCT008 Factitious Disorder 22 0.044
439
CLF029 Cleft Palate and Mental Retardation 21 0.044
440
IMG001 Image Syndrome 20 0.044
441
AND005 Androgen Insensitivity Syndrome, Mild 19 0.044
442
10Q001 10q22.3q23.3 Microdeletion Syndrome 19 0.044
443
EXT039 Extrapontine Myelinolysis 19 0.044
444
CMP061 Complete Lcat Deficiency 17 0.044
445
P OCL041 Oculomotor Apraxia Cogan Type 17 0.044
446
AML009 Amelogenesis Imperfecta Nephrocalcinosis 15 0.044
447
c CRB140 Cerebral Palsy, Spastic Quadriplegic, 2 8 0.044
448
CRH001 Crohn's Disease 78 0.040
449
P RTT002 Rett Syndrome 75 0.040
450
P DLT002 Dilated Cardiomyopathy 74 0.040
451
GLN003 Glanzmann's Thrombasthenia 68 0.040
452
GT001 Gout 66 0.040
453
DFC004 Deficiency Anemia 65 0.040
454
SKN016 Skin Disease 64 0.040
455
P FRD001 Friedreich Ataxia 64 0.040
456
PRC002 Paracoccidioidomycosis 64 0.040
457
PRC016 Pre-Eclampsia 64 0.040
458
c PRM002 Primary Hyperoxaluria 63 0.040
459
LNG024 Langerhans-Cell Histiocytosis 63 0.040
460
ISC006 Ischemic Heart Disease 62 0.040
461
ART005 Arteriovenous Malformation 62 0.040
462
HMP002 Hemophagocytic Lymphohistiocytosis 62 0.040
463
THR004 Thrombocytosis 61 0.040
464
P DGR001 Digeorge Syndrome 60 0.040
465
MLT001 Multiple Chemical Sensitivity 58 0.040
466
P PRM054 Primary Sclerosing Cholangitis 57 0.040
467
GNG013 Gingivitis 56 0.040
468
P SHR029 Short Syndrome 55 0.040
469
NPH051 Nephritis 55 0.040
470
LRN003 Learning Disability 54 0.040
471
SLP005 Sleep Disorder 54 0.040
472
TRD006 Tardive Dyskinesia 54 0.040
473
P PLY019 Polyneuropathy 54 0.040
474
CLL003 Cellulitis 53 0.040
475
c MYL007 Myeloma 53 0.040
476
PLY023 Polycystic Liver Disease 53 0.040
477
P ATN005 Autonomic Dysfunction 52 0.040
478
PST021 Postpartum Depression 52 0.040
479
BCT015 Bacteremia 52 0.040
480
P ALV004 Alveolar Rhabdomyosarcoma 51 0.040
481
ORL004 Oral Submucous Fibrosis 51 0.040
482
c MNT147 Mental Retardation 51 0.040
483
CLS010 Cluster Headache 51 0.040
484
P MYC008 Myocarditis 51 0.040
485
INT146 Intervertebral Disc Disease 50 0.040
486
LPC002 Lip Cancer 50 0.040
487
PLM010 Pulmonary Edema 50 0.040
488
c DNT011 Dentinogenesis Imperfecta 50 0.040
489
TXC012 Toxic Epidermal Necrolysis 49 0.040
490
NRP002 Neuroepithelioma 49 0.040
491
P LCT002 Lactose Intolerance 49 0.040
492
HDN002 Head Injury 49 0.040
493
BRS051 Breast Disease 48 0.040
494
P THR090 Thrombocythemia 1 48 0.040
495
CNV002 Conversion Disorder 48 0.040
496
c ACT078 Acute Porphyria 48 0.040
497
MRP001 Morphine Dependence 47 0.040
498
NRN002 Neuronitis 47 0.040
499
LKP004 Leukopenia 46 0.040
500
DRG002 Drug-Induced Hepatitis 46 0.040
501
c RSM001 Rasmussen Encephalitis 46 0.040
502
EXC002 Exocrine Pancreatic Insufficiency 45 0.040
503
c CPL003 Capillary Leak Syndrome 44 0.040
504
PRL019 Prolidase Deficiency 44 0.040
505
PYL006 Pyloric Stenosis 44 0.040
506
ESP025 Esophagus Adenocarcinoma 44 0.040
507
GST040 Gastric Adenocarcinoma 41 0.040
508
TBR008 Tuberculous Peritonitis 40 0.040
509
SZR006 Seizure Disorder 40 0.040
510
INC001 Incontinentia Pigmenti Achromians 39 0.040
511
HYP030 Hypoactive Sexual Desire Disorder 39 0.040
512
BGS001 Bagassosis 39 0.040
513
P HYP111 Hyperprolinemia 38 0.040
514
c VRL005 Viral Pneumonia 38 0.040
515
LYM045 Lymphocytic Vasculitis 38 0.040
516
EXT006 Extrahepatic Cholestasis 37 0.040
517
c SVR056 Severe Hemophilia a 35 0.040
518
ABD004 Abdominal Tuberculosis 35 0.040
519
IPX001 Ipex Syndrome 35 0.040
520
PTC001 Potocki-Shaffer Syndrome 35 0.040
521
URM005 Uremic Pruritus 34 0.040
522
ARC001 Arcus Senilis 34 0.040
523
MTR001 Mature Cataract 32 0.040
524
P DNS004 Duane Syndrome Type 2 31 0.040
525
CYC005 Cyclothymic Disorder 31 0.040
526
MYT004 Myotilinopathy 29 0.040
527
FBR064 Febrile Infection-Related Epilepsy Syndrome 29 0.040
528
END048 Endotoxin Hyporesponsiveness 28 0.040
529
SPR012 Separation Anxiety Disorder 27 0.040
530
NNH002 Non-a-E Hepatitis 27 0.040
531
SLS001 Sle Susceptibility 26 0.040
532
INS008 Insulin-Like Growth Factor I Deficiency 25 0.040
533
LKM059 Leukemia, Megakaryoblastic, with or Without Down Syndrome, Somatic 24 0.040
534
6Q1001 6q16 Deletion Syndrome 24 0.040
535
DYS009 Dysthymic Disorder 24 0.040
536
MYL002 Myelophthisic Anemia 24 0.040
537
MNS009 Monosomy 13q14 22 0.040
538
PNC077 Pancreatitis, Idiopathic 21 0.040
539
c FML139 Familial Myeloma 20 0.040
540
P 19P001 19p13.12 Microdeletion Syndrome 19 0.040
541
EPT021 Epithelial Recurrent Erosion Dystrophy 17 0.040
542
THY020 Thyroid Hyalinizing Trabecular Adenoma 16 0.040
543
OPT026 Optic Atrophy and Cataract, Autosomal Dominant 15 0.040
544
FCL021 Focal Cortical Dysplasia of Taylor 14 0.040
545
21Q002 21q22.13q22.2 Microdeletion Syndrome 14 0.040
546
TXC008 Toxic Optic Neuropathy 13 0.040
547
ESP037 Esophageal Cancer, Somatic 11 0.040
548
P MLT019 Multiple Myeloma 76 0.034
549
BRK003 Burkitt's Lymphoma 71 0.034
550
VSC007 Vascular Disease 69 0.034
551
P CHR089 Chronic Kidney Failure 68 0.034
552
ADD001 Addison's Disease 68 0.034
553
P NRC002 Narcolepsy 67 0.034
554
DBT001 Diabetic Ketoacidosis 67 0.034
555
c THR014 Thrombocytopenia 66 0.034
556
P HMP004 Hemophilia B 66 0.034
557
ACT033 Acute Intermittent Porphyria 66 0.034
558
P CNG026 Congenital Heart Defect 65 0.034
559
c LPS004 Lupus Erythematosus 65 0.034
560
c HYP095 Hypercholesterolemia 65 0.034
561
P ATP001 Atopic Dermatitis 64 0.034
562
HYP020 Hyperprolactinemia 64 0.034
563
P GRV001 Graves' Disease 63 0.034
564
P MGR002 Migraine 61 0.034
565
P BLR001 Biliary Atresia 60 0.034
566
P HYD006 Hydrocephalus 60 0.034
567
P ATS007 Autism Spectrum Disorder 59 0.034
568
P LBR002 Leber Hereditary Optic Neuropathy 59 0.034
569
PRT011 Protein C Deficiency 59 0.034
570
P RHN004 Rhinitis 59 0.034
571
SKN014 Skin Cancer 58 0.034
572
ZLL002 Zollinger-Ellison Syndrome 58 0.034
573
GST009 Gastroschisis 58 0.034
574
c ATX004 Ataxia 56 0.034
575
c MLR021 Malaria, Severe 56 0.034
576
c ENC004 Encephalitis 56 0.034
577
CRD137 Cardiogenic Shock 56 0.034
578
P MLN008 Melanoma 56 0.034
579
ACT049 Acute Disseminated Encephalomyelitis 56 0.034
580
HPT022 Hepatoblastoma 56 0.034
581
PLS006 Plasmodium Vivax Malaria 56 0.034
582
VSC002 Vascular Dementia 55 0.034
583
P CND004 Candidiasis 55 0.034
584
DDN006 Duodenitis 54 0.034
585
SRC014 Sarcoma 54 0.034
586
HNT002 Hantavirus Pulmonary Syndrome 54 0.034
587
P BRN009 Burning Mouth Syndrome 54 0.034
588
c MCR010 Microcephaly 54 0.034
589
TWN003 Townes-Brocks Syndrome 53 0.034
590
ACR003 Acrodermatitis Enteropathica 53 0.034
591
ANG018 Angiomyolipoma 52 0.034
592
CHR074 Choriocarcinoma 52 0.034
593
KLB001 Klebsiella 51 0.034
594
ART004 Aortic Atherosclerosis 51 0.034
595
c ATM024 Autoimmune Pancreatitis 51 0.034
596
P INT068 Intestinal Disease 51 0.034
597
CHL004 Cholelithiasis 50 0.034
598
RFR010 Refractory Anemia 50 0.034
599
c CNG018 Congenital Heart Block 50 0.034
600
PRC003 Proctitis 49 0.034
601
c SCL009 Sclerosing Cholangitis 49 0.034
602
STT004 Steatorrhea 49 0.034
603
P GLC007 Glaucoma 49 0.034
604
SCR002 Scurvy 48 0.034
605
MTB004 Metabolic Acidosis 48 0.034
606
LRY018 Laryngeal Squamous Cell Carcinoma 47 0.034
607
RTN025 Retinoschisis 47 0.034
608
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 46 0.034
609
P KRT007 Keratoconus 46 0.034
610
MMM001 Mammary Paget's Disease 46 0.034
611
P KRN004 Kernicterus 46 0.034
612
CHL061 Childhood Leukemia 46 0.034
613
PLR008 Pleurisy 46 0.034
614
GST045 Gastroenteritis 46 0.034
615
ACR005 Acrodermatitis 45 0.034
616
P CMP008 Compartment Syndrome 45 0.034
617
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 45 0.034
618
AXN001 Axonal Neuropathy 44 0.034
619
HYP026 Hypoglycemic Coma 43 0.034
620
GNG008 Ganglioneuroblastoma 43 0.034
621
KWS001 Kwashiorkor 43 0.034
622
KRT002 Keratomalacia 42 0.034
623
FSH001 Fish-Eye Disease 41 0.034
624
DNR001 Duane Retraction Syndrome 41 0.034
625
ART002 Arts Syndrome 40 0.034
626
NCR007 Necrotizing Fasciitis 40 0.034
627
CHR010 Chorioangioma 40 0.034
628
FST010 Fasting Hypoglycemia 40 0.034
629
OPS001 Opisthorchiasis 39 0.034
630
GST039 Gastroduodenitis 39 0.034
631
PRP009 Peripartum Cardiomyopathy 39 0.034
632
PNC033 Pancreas Adenocarcinoma 39 0.034
633
MRS001 Marasmus 39 0.034
634
ENT007 Enteropathica 38 0.034
635
PLM074 Pulmonary Function 38 0.034
636
SXL003 Sexual Disorder 38 0.034
637
SPC005 Speech Disorder 38 0.034
638
P PLN008 Peeling Skin Syndrome 38 0.034
639
MSS002 Mass Syndrome 37 0.034
640
SPR017 Spermatocele 36 0.034
641
FRN014 Fournier Gangrene 36 0.034
642
HPT004 Hepatic Coma 36 0.034
643
SPN060 Spondylocarpotarsal Synostosis Syndrome 36 0.034
644
FBR063 Fibrocalculous Pancreatic Diabetes 34 0.034
645
INT079 Intrahepatic Cholangiocarcinoma 34 0.034
646
ESP027 Esophagus Squamous Cell Carcinoma 34 0.034
647
c CNG013 Congenital Disorder of Glycosylation Type I 33 0.034
648
DYS036 Dysequilibrium Syndrome 32 0.034
649
HMC004 Homocysteine Plasma Level 31 0.034
650
MCR029 Micro Syndrome 31 0.034
651
CRB027 Cerebellar Disease 30 0.034
652
FRN031 Frontotemporal Lobar Degeneration with Ubiquitin-Positive Inclusions 29 0.034
653
SCH057 Schizensephaly 29 0.034
654
c HMC010 Hemochromatosis, Type 3 27 0.034
655
AML006 Amelogenesis Imperfecta Hypoplastic Type, Ig 23 0.034
656
HYP085 Hypothalamic Disease 22 0.034
657
NRT006 North American Indian Childhood Cirrhosis 22 0.034
658
MNT002 Mental Depression 21 0.034
659
ART030 Aortic Arch Interruption 21 0.034
660
PNC034 Pancreas Disease 18 0.034
661
MLD004 Mal De Debarquement 15 0.034
662
VST006 Vestibulocochlear Nerve Disease 15 0.034
663
AMY010 Amyloidosis Beta2m 13 0.034
664
GLC008 Glucose Metabolism Disease 13 0.034
665
P AMY001 Amyotrophic Lateral Sclerosis 87 0.028
666
P RHM011 Rheumatoid Arthritis 83 0.028
667
PHN003 Phenylketonuria 77 0.028
668
P WSK001 Wiskott-Aldrich Syndrome 76 0.028
669
P LFR001 Li-Fraumeni Syndrome 75 0.028
670
P RFS001 Refsum Disease 73 0.028
671
c NNN003 Noonan Syndrome 73 0.028
672
P TYP020 Type 1 Diabetes 73 0.028
673
P HRS001 Hirschsprung's Disease 72 0.028
674
c TYP008 Type 1 Diabetes Mellitus 71 0.028
675
P TRN020 Turner Syndrome 71 0.028
676
AGR001 Age Related Macular Degeneration 71 0.028
677
KWS002 Kawasaki Disease 69 0.028
678
NRL016 Neural Tube Defects 69 0.028
679
ACT074 Acute Lymphocytic Leukemia 69 0.028
680
THL005 Thalassemia 69 0.028
681
STR067 Stroke, Ischemic 69 0.028
682
P CRN008 Carney Complex 68 0.028
683
PRG004 Progeria 68 0.028
684
ASP006 Aspergillosis 68 0.028
685
SCK003 Sickle Cell Anemia 67 0.028
686
P LPR003 Leprosy 67 0.028
687
P FRN006 Frontotemporal Dementia 66 0.028
688
P LSH001 Leishmaniasis 65 0.028
689
P THR015 Thrombophilia 65 0.028
690
ABT001 Abetalipoproteinemia 64 0.028
691
P MLT007 Multiple Epiphyseal Dysplasia 63 0.028
692
THR079 Thromboembolism 63 0.028
693
SML001 Small Cell Carcinoma 62 0.028
694
PLM001 Pulmonary Tuberculosis 62 0.028
695
BRR003 Barrett's Esophagus 62 0.028
696
P HLP001 Holoprosencephaly 61 0.028
697
VLV011 Vulvovaginal Candidiasis 61 0.028
698
c THY032 Thyroiditis 61 0.028
699
LMY002 Leiomyoma 61 0.028
700
HYP266 Hypoxia 60 0.028
701
PND002 Pendred Syndrome 60 0.028
702
P RSP003 Respiratory Failure 60 0.028
703
P ATM006 Autoimmune Lymphoproliferative Syndrome 60 0.028
704
TYP007 Typhoid Fever 60 0.028
705
PPL022 Papilloma 60 0.028
706
P JVN005 Juvenile Myoclonic Epilepsy 59 0.028
707
DBT010 Diabetic Neuropathy 59 0.028
708
VTL002 Vitiligo 59 0.028
709
c HYP086 Hypothyroidism 59 0.028
710
TRG002 Trigeminal Neuralgia 59 0.028
711
P MLG068 Malignant Glioma 58 0.028
712
FCT006 Factor V Deficiency 58 0.028
713
SCK005 Sickle Cell Disease 58 0.028
714
CRB021 Cerebral Malaria 58 0.028
715
SMT015 Smith Magenis Syndrome 58 0.028
716
P CMP010 Complex Regional Pain Syndrome 57 0.028
717
CRB042 Cerebellar Ataxia 57 0.028
718
CMP002 Campylobacteriosis 56 0.028
719
STS002 Situs Inversus 56 0.028
720
ASP003 Aseptic Meningitis 56 0.028
721
ERY003 Erythema Multiforme 56 0.028
722
P MTB001 Metabolic Syndrome X 56 0.028
723
TST014 Testicular Cancer 55 0.028
724
BRN004 Brain Edema 55 0.028
725
c HRM001 Hermansky-Pudlak Syndrome 55 0.028
726
THR009 Thrombocytopenia-Absent Radius Syndrome 55 0.028
727
SNS001 Sensorineural Hearing Loss 55 0.028
728
TRN015 Transient Cerebral Ischemia 55 0.028
729
FDL002 Food Allergy 55 0.028
730
HYP080 Hypogonadism 54 0.028
731
FLT001 Felty's Syndrome 54 0.028
732
c SVR001 Severe Acute Respiratory Syndrome 54 0.028
733
VNS010 Venous Thromboembolism 54 0.028
734
HLL004 Hellp Syndrome 54 0.028
735
MGL001 Megaloblastic Anemia 54 0.028
736
LPD010 Lipodystrophy 53 0.028
737
VRG001 Variegate Porphyria 53 0.028
738
GLL018 Gallbladder Cancer 53 0.028
739
c THN001 Thanatophoric Dysplasia 53 0.028
740
P STR020 Strabismus 53 0.028
741
ACR008 Acrocallosal Syndrome 53 0.028
742
P OVR049 Ovarian Disease 53 0.028
743
SPN020 Spondylosis 53 0.028
744
DYS014 Dyspepsia 52 0.028
745
P EPL002 Epilepsy Syndrome 52 0.028
746
HYP003 Hypermethioninemia 52 0.028
747
GNR005 Gonorrhea 52 0.028
748
KRT001 Keratoconjunctivitis Sicca 52 0.028
749
KRT006 Keratoconjunctivitis 52 0.028
750
c CNT035 Central Nervous System Disease 52 0.028
751
PRN011 Pernicious Anemia 52 0.028
752
P GLL020 Gallbladder Disease 52 0.028
753
GNG002 Ganglioneuroma 51 0.028
754
c SYN005 Synostosis 51 0.028
755
ARC002 Arachnoiditis 51 0.028
756
LYM027 Lymphopenia 51 0.028
757
P RPD001 Rapidly Progressive Glomerulonephritis 51 0.028
758
BTL001 Botulism 51 0.028
759
P HYP027 Hypobetalipoproteinemia 51 0.028
760
HYP006 Hypertensive Heart Disease 51 0.028
761
ERY008 Erythromelalgia 51 0.028
762
P SCL015 Scleritis 50 0.028
763
LYM021 Lymphadenitis 50 0.028
764
ART008 Arteriosclerosis Obliterans 50 0.028
765
HYP005 Hypokalemia 50 0.028
766
AMY053 Amyloidosis, Secondary 50 0.028
767
GST050 Gastrointestinal System Disease 50 0.028
768
c CTR001 Citrullinemia 50 0.028
769
MNN009 Meningoencephalitis 49 0.028
770
RTN018 Retinal Disease 49 0.028
771
P PRT029 Parathyroid Adenoma 49 0.028
772
c DRR001 Diarrhea 49 0.028
773
TNG003 Tongue Cancer 49 0.028
774
MDS022 Mediastinitis 49 0.028
775
SPS019 Spastic Paraparesis 49 0.028
776
CLL002 Collecting Duct Carcinoma 48 0.028
777
ANG054 Angina Pectoris 48 0.028
778
c FML016 Familial Hypertriglyceridemia 48 0.028
779
c RTN014 Retinal Artery Occlusion 47 0.028
780
ELS001 Eales Disease 47 0.028
781
PRT070 Peritoneal Carcinoma 47 0.028
782
SKN019 Skin Melanoma 47 0.028
783
PRC012 Pericardial Effusion 47 0.028
784
P DYS026 Dysfibrinogenemia 46 0.028
785
LRG008 Large Granular Lymphocyte Leukemia 46 0.028
786
NDL007 Nodular Goiter 46 0.028
787
LGN001 Legionnaires' Disease 46 0.028
788
VRC005 Varicose Veins 46 0.028
789
PRT026 Parotitis 45 0.028
790
NPH004 Nephropathia Epidemica 45 0.028
791
3MS001 3-M Syndrome 45 0.028
792
BLD044 Bladder Disease 45 0.028
793
P PLY024 Polymicrogyria 45 0.028
794
DMP001 Dumping Syndrome 45 0.028
795
OST097 Osteoporotic Fracture 44 0.028
796
GST029 Gastric Cardia Adenocarcinoma 44 0.028
797
MYC013 Mycobacterium Abscessus 44 0.028
798
NLS001 Nelson Syndrome 44 0.028
799
PRS042 Prostate Disease 44 0.028
800
ADN027 Adenomyosis 44 0.028
801
LCT001 Lactic Acidosis 44 0.028
802
SDR003 Sideroblastic Anemia 44 0.028
803
ANR009 Aneurysmal Bone Cysts 43 0.028
804
ATR057 Atrioventricular Block 43 0.028
805
c INT064 Intermediate Uveitis 43 0.028
806
P PRG011 Progressive Myoclonus Epilepsy 43 0.028
807
MNN021 Meningococcemia 42 0.028
808
SPS057 Spasticity 42 0.028
809
DVL002 Developmental Disabilities 42 0.028
810
c LNG063 Lung Cancer Susceptibility 42 0.028
811
BRN014 Bronchopneumonia 42 0.028
812
HPT008 Hepatic Tuberculosis 41 0.028
813
NRL007 Neurologic Diseases 41 0.028
814
P ORF002 Orofacial Cleft 41 0.028
815
STR001 Striatonigral Degeneration 41 0.028
816
THL010 Thalassemia Minor 40 0.028
817
ANX004 Anoxia 40 0.028
818
c MYC026 Myoclonus Epilepsy 40 0.028
819
MCR017 Macrocytic Anemia 40 0.028
820
STC004 Stachybotrys Chartarum 39 0.028
821
SNL007 Senile Cataract 39 0.028
822
NRM003 Norum Disease 39 0.028
823
c MGR001 Migraine Without Aura 39 0.028
824
c MGR003 Migraine with Aura 38 0.028
825
TCD001 Tic Disorder 38 0.028
826
INT080 Intraocular Melanoma 38 0.028
827
IMP006 Impulse Control Disorder 37 0.028
828
PRL008 Paralytic Ileus 37 0.028
829
ESP002 Esophageal Varix 37 0.028
830
SPC004 Specific Phobia 36 0.028
831
CNT060 Central Serous Chorioretinopathy 35 0.028
832
CRY008 Cryopyrin-Associated Periodic Syndrome 35 0.028
833
BLD054 Blood Protein Disease 35 0.028
834
VRL011 Viral Infectious Disease 35 0.028
835
RTR001 Retrograde Amnesia 34 0.028
836
P 2Q3002 2q37 Microdeletion Syndrome 34 0.028
837
ARC004 Arc Syndrome 34 0.028
838
ADR021 Adrenocorticotropic Hormone Deficiency 34 0.028
839
ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 34 0.028
840
LNG038 Lung Small Cell Carcinoma 33 0.028
841
PNC041 Pancreatic Ductal Adenocarcinoma 32 0.028
842
ACT084 Acute Stress Disorder 32 0.028
843
BDS002 Bod Syndrome 32 0.028
844
ACT099 Acute Fatty Liver of Pregnancy 32 0.028
845
BRD005 Borderline Leprosy 32 0.028
846
OBS019 Obesity, Variation in 31 0.028
847
SCH011 Schizotypal Personality Disorder 31 0.028
848
GRN009 Granulomatous Hepatitis 31 0.028
849
MTC028 Mitochondrial Cardiomyopathy 31 0.028
850
DPR013 Dopa-Responsive Cervical Dystonia 31 0.028
851
OPT006 Optic Nerve Disease 29 0.028
852
INT025 Intermittent Explosive Disorder 28 0.028
853
PTL001 Patulous Eustachian Tube 28 0.028
854
MNR012 M�ni�re Disease 28 0.028
855
c HVY001 Heavy Chain Disease 27 0.028
856
PLS002 Peliosis Hepatis 26 0.028
857
c 2P2001 2p21 Microdeletion Syndrome 25 0.028
858
HV1005 Hiv-1 Viremia 25 0.028
859
MNN024 Meningitis and Encephalitis 24 0.028
860
c CRN174 Coronary Heart Disease 2 23 0.028
861
c ATM007 Autoimmune Disease of Central Nervous System 22 0.028
862
P CHR259 Chromosome 6q25 Microdeletion Syndrome 22 0.028
863
AVD001 Avoidant Personality Disorder 21 0.028
864
MYC021 Mycobacterium Xenopi 20 0.028
865
c MCH003 Mu Chain Disease 20 0.028
866
ETH012 Ethylene Glycol Poisoning 19 0.028
867
c KRN003 Kernicterus Due to Isoimmunization 18 0.028
868
MTR016 Maternal Hyperphenylalaninemia 17 0.028
869
DSS008 Disease of Mental Health 17 0.028
870
GRN014 Grn-Related Frontotemporal Dementia 16 0.028
871
PL2001 Pla2g6-Associated Neurodegeneration 14 0.028
872
CRB089 Cerebral Beriberi 14 0.028
873
SPT001 Septal Myocardial Infarction 13 0.028
874
GST028 Gastric Squamous Cell Carcinoma 13 0.028
875
P FML045 Familial Mosaic Monosomy 7 Syndrome 11 0.028
876
CHL090 Cholesterol Desmolase-Deficient Congenital Adrenal Hyperplasia 10 0.028
877
ATY022 Atypical Coarctation of Aorta 8 0.028
878
P SYS001 Systemic Lupus Erythematosus 83 0.020
879
CDS001 Cadasil 80 0.020
880
HDG007 Hodgkin's Lymphoma 80 0.020
881
ACH004 Achondroplasia 77 0.020
882
APL001 Aplastic Anemia 77 0.020
883
P FML021 Familial Hypercholesterolemia 76 0.020
884
P ART022 Arthritis 75 0.020
885
P LBR001 Leber Congenital Amaurosis 74 0.020
886
P FML018 Familial Mediterranean Fever 73 0.020
887
KPS001 Kaposi's Sarcoma 73 0.020
888
OVR042 Ovarian Cancer 73 0.020
889
P OST012 Osteoarthritis 72 0.020
890
MYL040 Myelodysplastic Syndromes 72 0.020
891
ATS001 Autistic Disorder 71 0.020
892
P CLC005 Celiac Disease 71 0.020
893
MNK001 Menkes Disease 71 0.020
894
CST001 Costello Syndrome 71 0.020
895
DCH001 Duchenne Muscular Dystrophy 70 0.020
896
P AST007 Astrocytoma 70 0.020
897
WRN001 Werner Syndrome 68 0.020
898
GST023 Gastric Ulcer 67 0.020
899
P MLR004 Malaria 66 0.020
900
P PLY011 Polycystic Ovary Syndrome 66 0.020
901
P ABD003 Abdominal Aortic Aneurysm 65 0.020
902
BRN028 Brain Cancer 65 0.020
903
P ART023 Arthropathy 65 0.020
904
P RCK004 Rickets 65 0.020
905
VSC011 Vasculitis 65 0.020
906
TNG002 Tangier Disease 64 0.020
907
STT001 Status Epilepticus 64 0.020
908
P GRF002 Graft Versus Host Disease 64 0.020
909
ART021 Arteriosclerosis 63 0.020
910
CHR066 Chronic Fatigue Syndrome 63 0.020
911
SPN038 Spina Bifida 63 0.020
912
P SYS005 Systemic Scleroderma 63 0.020
913
CHR012 Chronic Granulomatous Disease 63 0.020
914
ACT073 Acute Leukemia 62 0.020
915
c CRN037 Craniosynostosis 62 0.020
916
P BRN022 Bronchiectasis 62 0.020
917
ART016 Aortic Aneurysm 62 0.020
918
BSL007 Basal Cell Carcinoma 62 0.020
919
P MTH008 Methylmalonic Acidemia 62 0.020
920
HMN010 Hemangioma 62 0.020
921
URT039 Urticaria 61 0.020
922
P END044 Endometriosis 61 0.020
923
HRP004 Herpes Zoster 60 0.020
924
BRN002 Bronchiolitis 60 0.020
925
P NRB001 Neuroblastoma 60 0.020
926
P OST009 Osteochondritis Dissecans 60 0.020
927
TXC005 Toxic Shock Syndrome 60 0.020
928
PPL002 Papillary Carcinoma 60 0.020
929
HML002 Hemolytic Anemia 60 0.020
930
P PRN023 Prion Disease 60 0.020
931
SPT014 Septo-Optic Dysplasia 59 0.020
932
c ACT075 Acute Myocardial Infarction 59 0.020
933
P SLV001 Silver-Russell Syndrome 59 0.020
934
BLS001 Blau Syndrome 59 0.020
935
LPR001 Lepromatous Leprosy 59 0.020
936
INS001 Insulinoma 59 0.020
937
DSS009 Disseminated Intravascular Coagulation 59 0.020
938
GLB001 Gilbert Syndrome 59 0.020
939
HPT002 Hepatic Vein Thrombosis 59 0.020
940
CYS005 Cysticercosis 59 0.020
941
SHW002 Shwachman-Diamond Syndrome 58 0.020
942
CRB037 Cerebral Palsy 58 0.020
943
P BRN012 Bronchiolitis Obliterans 58 0.020
944
PSD007 Pseudomyxoma Peritonei 58 0.020
945
P VLC001 Velocardiofacial Syndrome 57 0.020
946
FCL008 Focal Glomerulosclerosis 57 0.020
947
INT051 Intussusception 57 0.020
948
ADR008 Adrenal Adenoma 57 0.020
949
MLL005 Miller-Dieker Syndrome 57 0.020
950
P FRG001 Fragile X Syndrome 57 0.020
951
P HYP024 Hypoparathyroidism 57 0.020
952
P HRP006 Herpes Simplex 57 0.020
953
ACH005 Achalasia 57 0.020
954
SLP006 Sleep Apnea 57 0.020
955
P DBT005 Diabetes Insipidus 56 0.020
956
P HYP040 Hypospadias 56 0.020
957
P VRL007 Viral Encephalitis 56 0.020
958
P OLG002 Oligodendroglioma 56 0.020
959
NTH001 Netherton Syndrome 56 0.020
960
c ATM011 Autoimmune Hepatitis 56 0.020
961
KRT004 Keratitis 56 0.020
962
CLS007 Classic Kaposi Sarcoma 56 0.020
963
TTR001 Tetralogy of Fallot 55 0.020
964
c BRG001 Brugada Syndrome 55 0.020
965
c ACT135 Acute Graft Versus Host Disease 55 0.020
966
c CNG042 Congenital Central Hypoventilation Syndrome 55 0.020
967
ATM010 Autoimmune Hemolytic Anemia 55 0.020
968
c HYP060 Hyperinsulinism 55 0.020
969
ERY009 Erythropoietic Protoporphyria 55 0.020
970
c HYP076 Hyperthyroidism 55 0.020
971
c SYP003 Syphilis 55 0.020
972
P PLM006 Pulmonary Alveolar Proteinosis 55 0.020
973
GNG004 Ganglioglioma 54 0.020
974
GTL001 Gitelman Syndrome 54 0.020
975
ALP007 Alpha 1-Antitrypsin Deficiency 54 0.020
976
NRM002 Normal Pressure Hydrocephalus 54 0.020
977
c VNT002 Ventricular Septal Defect 54 0.020
978
PYR013 Pyruvate Kinase Deficiency 54 0.020
979
ESP020 Esophageal Atresia 54 0.020
980
c MSC005 Muscular Dystrophy 54 0.020
981
LYM040 Lymphoblastic Lymphoma 54 0.020
982
GLL031 Guillain-Barr� Syndrome 54 0.020
983
GST037 Gastroparesis 54 0.020
984
P LRY019 Laryngitis 53 0.020
985
c FML035 Familial Hyperlipidemia 53 0.020
986
P OMP004 Omphalocele 53 0.020
987
VSC006 Vascular Cancer 53 0.020
988
DBF001 D-Bifunctional Protein Deficiency 53 0.020
989
P CTN003 Cutaneous Lupus Erythematosus 53 0.020
990
CRB039 Cerebrovascular Disease 53 0.020
991
P HYP083 Hypopituitarism 53 0.020
992
PRG009 Progressive Multifocal Leukoencephalopathy 53 0.020
993
GSG001 Gas Gangrene 53 0.020
994
PRD007 Periodontal Disease 53 0.020
995
CHR005 Chorioamnionitis 52 0.020
996
BRN080 Brain Ischemia 52 0.020
997
PNM001 Pneumocystosis 52 0.020
998
P MMB001 Membranoproliferative Glomerulonephritis 52 0.020
999
APR001 Apraxia 52 0.020
1000
c ATN004 Autonomic Neuropathy 52 0.020
1001
ALV002 Alveolar Echinococcosis 52 0.020
1002
CNN003 Conn's Syndrome 52 0.020
1003
NRH001 Neurohypophyseal Diabetes Insipidus 52 0.020
1004
RHM027 Rheumatic Disease 52 0.020
1005
c BCT007 Bacterial Meningitis 52 0.020
1006
HML001 Hemolytic-Uremic Syndrome 52 0.020
1007
CYT005 Cytomegalovirus Retinitis 52 0.020
1008
DBT062 Diabetic Foot Ulcers 52 0.020
1009
P CNG015 Congenital Diaphragmatic Hernia 52 0.020
1010
DNG003 Dengue Disease 52 0.020
1011
GRD001 Giardiasis 51 0.020
1012
c SPN049 Spinocerebellar Ataxia 51 0.020
1013
IDP064 Idiopathic Neutropenia 51 0.020
1014
c PRM010 Primary Open Angle Glaucoma 51 0.020
1015
PLC007 Placental Abruption 51 0.020
1016
RNL014 Renal Cell Carcinoma 51 0.020
1017
AMB001 Amebiasis 51 0.020
1018
MNC007 Monocytic Leukemia 51 0.020
1019
P OPN001 Open-Angle Glaucoma 51 0.020
1020
c TRC011 Treacher Collins Syndrome 51 0.020
1021
END031 Endometrial Stromal Sarcoma 51 0.020
1022
GLC036 Glucagonoma 51 0.020
1023
ANK001 Ankylosis 51 0.020
1024
P NRV007 Nervous System Disease 51 0.020
1025
CNN005 Connective Tissue Disease 51 0.020
1026
PRS047 Prostatitis 50 0.020
1027
LPP001 Lipoprotein Lipase Deficiency 50 0.020
1028
P PNM006 Pneumoconiosis 50 0.020
1029
FSC002 Fascioliasis 50 0.020
1030
SLD003 Sialadenitis 50 0.020
1031
TCL004 T-Cell Leukemia 50 0.020
1032
LYM026 Lymphoblastic Leukemia 49 0.020
1033
CRT016 Carotid Artery Disease 49 0.020
1034
PLY012 Polyhydramnios 49 0.020
1035
ACT103 Acute Lymphoblastic Leukemia, Childhood 49 0.020
1036
EXS001 Exostosis 49 0.020
1037
c MYT002 Myotonic Dystrophy 49 0.020
1038
SCH002 Schnitzler Syndrome 49 0.020
1039
INT067 Interstitial Nephritis 49 0.020
1040
CHL056 Cheilitis 49 0.020
1041
ENC006 Encephalomyelitis 49 0.020
1042
P TMT001 Timothy Syndrome 48 0.020
1043
c ERY013 Erythrocytosis 48 0.020
1044
P DYS021 Dysautonomia 48 0.020
1045
TRY001 Trypanosomiasis 48 0.020
1046
c CTR002 Cataract 48 0.020
1047
TCL002 T-Cell Large Granular Lymphocyte Leukemia 48 0.020
1048
ANV001 Anovulation 48 0.020
1049
END040 Endogenous Depression 48 0.020
1050
P KLP003 Klippel-Feil Syndrome 48 0.020
1051
c FBR031 Febrile Seizures 48 0.020
1052
CRN024 Corneal Disease 48 0.020
1053
UTR039 Uterine Fibroid 48 0.020
1054
PLM070 Pulmonic Stenosis 48 0.020
1055
CRD005 Cardia Cancer 48 0.020
1056
HYP025 Hyperphosphatemia 48 0.020
1057
NRR001 Neuroretinitis 48 0.020
1058
P GRN010 Granular Cell Tumor 48 0.020
1059
P END047 Endophthalmitis 48 0.020
1060
HMG005 Hemoglobinopathy 47 0.020
1061
P NGH001 Night Blindness 47 0.020
1062
CLF001 Cleft Lip 47 0.020
1063
RHZ001 Rhizomelic Chondrodysplasia Punctata 47 0.020
1064
YLL001 Yellow Nail Syndrome 47 0.020
1065
IMM001 Immune-Complex Glomerulonephritis 47 0.020
1066
ANG011 Angiodysplasia 47 0.020
1067
SHH001 Sheehan Syndrome 47 0.020
1068
PLM016 Pleomorphic Carcinoma 47 0.020
1069
IMP005 Impotence 47 0.020
1070
ILS001 Ileus 47 0.020
1071
GST060 Gastric Cancer, Somatic 47 0.020
1072
SPR016 Spermatic Cord Torsion 47 0.020
1073
VSM001 Vasomotor Rhinitis 46 0.020
1074
c INT070 Intestinal Obstruction 46 0.020
1075
PRP034 Purpura Fulminans 46 0.020
1076
CHN015 Chondrodysplasia 46 0.020
1077
SMT006 Somatoform Disorder 46 0.020
1078
HPT067 Hepatocellular Adenoma 46 0.020
1079
JVN033 Juvenile Nasopharyngeal Angiofibroma 46 0.020
1080
PRT019 Protein-Losing Enteropathy 46 0.020
1081
NRT004 Neuritis 46 0.020
1082
CRN006 Coronary Aneurysm 45 0.020
1083
CRN029 Coronary Arteriosclerosis 45 0.020
1084
BRS081 Breast Cancer Susceptibility 45 0.020
1085
ACR006 Aceruloplasminemia 45 0.020
1086
SYM002 Sympathetic Ophthalmia 45 0.020
1087
CLN003 Clonorchiasis 45 0.020
1088
NWB001 Newborn Respiratory Distress Syndrome 45 0.020
1089
FRY002 Fryns Syndrome 45 0.020
1090
ORL013 Oral Lichen Planus 45 0.020
1091
P THN004 Thanatophoric Dysplasia Type 1 45 0.020
1092
P BRS044 Breast Adenocarcinoma 45 0.020
1093
SCB001 Scabies 45 0.020
1094
c HYP273 Hypothyroidism, Congenital, Due to Thyroid Dysgenesis or Hypoplasia 45 0.020
1095
FRN002 Frontal Lobe Epilepsy 44 0.020
1096
P OVR046 Ovarian Cyst 44 0.020
1097
P INF037 Inflammatory Bowel Disease 44 0.020
1098
P AZS001 Azoospermia 44 0.020
1099
c CNT048 Central Hypoventilation Syndrome 44 0.020
1100
PTR001 Petrositis 44 0.020
1101
c HRP009 Herpes Simplex Encephalitis 44 0.020
1102
c PRK031 Parkinson Disease 1 44 0.020
1103
SBP001 Subependymal Giant Cell Astrocytoma 44 0.020
1104
DSC009 Discoid Lupus Erythematosus 44 0.020
1105
GNG005 Gangliocytoma 44 0.020
1106
ANP009 Anaplastic Oligodendroglioma 44 0.020
1107
FML164 Familial Hdl Deficiency 43 0.020
1108
AFR002 African Tick-Bite Fever 43 0.020
1109
PLM035 Pulmonary Eosinophilia 43 0.020
1110
PRV006 Pervasive Developmental Disorder 43 0.020
1111
ESN006 Eosinophilic Meningitis 43 0.020
1112
ASP007 Aspiration Pneumonia 43 0.020
1113
RLY001 Riley-Day Syndrome 43 0.020
1114
c STC001 Stickler Syndrome 43 0.020
1115
CTY001 Cat Eye Syndrome 43 0.020
1116
ANG002 Angiostrongyliasis 42 0.020
1117
TKT001 Tako-Tsubo Cardiomyopathy 42 0.020
1118
DYS073 Dysphagia 42 0.020
1119
PST055 Postural Hypotension 42 0.020
1120
SQM007 Squamous Cell Carcinoma of the Head and Neck 42 0.020
1121
NNT012 Neonatal Jaundice 42 0.020
1122
BLL007 Bullous Skin Disease 42 0.020
1123
c PRM108 Primary Progressive Multiple Sclerosis 42 0.020
1124
LNG029 Lung Adenocarcinoma 42 0.020
1125
PRP002 Periapical Granuloma 42 0.020
1126
CHR286 Chronic Neutrophilic Leukemia 42 0.020
1127
MLN003 Melancholia 42 0.020
1128
PLP001 Pulpitis 41 0.020
1129
CMP009 Complement Deficiency 41 0.020
1130
CNG045 Congenital Dyserythropoietic Anemia Type I 41 0.020
1131
SPS007 Spastic Cerebral Palsy 41 0.020
1132
c OPT004 Optic Atrophy 41 0.020
1133
CLN015 Colon Adenocarcinoma 41 0.020
1134
GLS007 Glossitis 40 0.020
1135
ETH004 Euthyroid Sick Syndrome 40 0.020
1136
c FML085 Familial Prostate Cancer 40 0.020
1137
BNG016 Benign Migratory Glossitis 40 0.020
1138
CRN025 Corneal Dystrophy 40 0.020
1139
INT052 Intestinal Volvulus 40 0.020
1140
RCT011 Rectal Prolapse 40 0.020
1141
FTL007 Fetal Hydantoin Syndrome 40 0.020
1142
LPD004 Lipoid Nephrosis 40 0.020
1143
P CNG025 Congenital Disorder of Glycosylation 39 0.020
1144
CRB008 Cerebral Atherosclerosis 39 0.020
1145
c HYP263 Hypersomnia 39 0.020
1146
c CRT018 Carotid Intimal Medial Thickness 39 0.020
1147
IGG001 Iga Glomerulonephritis 39 0.020
1148
CNG219 Congenital Aural Atresia 39 0.020
1149
c HYP052 Hyperkalemic Periodic Paralysis 39 0.020
1150
LPP002 Lipoprotein Glomerulopathy 39 0.020
1151
SML026 Small Fiber Neuropathy 39 0.020
1152
GLT007 Glutathione Synthetase Deficiency 39 0.020
1153
ISL005 Isolated Acth Deficiency 39 0.020
1154
HTS001 Hiatus Hernia 39 0.020
1155
NRN005 Neuronal Ceroid-Lipofuscinoses 38 0.020
1156
RBF001 Riboflavin Deficiency 38 0.020
1157
ENC014 Enchondroma 38 0.020
1158
EXN003 Exencephaly 38 0.020
1159
P TST015 Testicular Disease 38 0.020
1160
PRN014 Paronychia 38 0.020
1161
CRB036 Cerebral Meningioma 38 0.020
1162
PLR007 Pleural Empyema 37 0.020
1163
VCL001 Vacuolar Myopathy 37 0.020
1164
MRC003 Mercury Poisoning 37 0.020
1165
LMB050 Limbal Stem Cell Deficiency 37 0.020
1166
AGN001 Aagenaes Syndrome 37 0.020
1167
FNS001 Funisitis 37 0.020
1168
c ADL027 Adult Dermatomyositis 37 0.020
1169
HYD028 Hydrops, Ectopic Calcification, Moth-Eaten Skeletal Dysplasia 37 0.020
1170
DDN004 Duodenogastric Reflux 37 0.020
1171
PNV001 Panuveitis 36 0.020
1172
PLM038 Pulmonary Large Cell Neuroendocrine Carcinoma 36 0.020
1173
PLR005 Pleuropneumonia 36 0.020
1174
5QS001 5q- Syndrome 36 0.020
1175
c FML169 Familial Osteochondritis Dissecans 36 0.020
1176
c DBT031 Diabetes, Type 2 36 0.020
1177
PST062 Pustulosis Palmaris Et Plantaris 36 0.020
1178
BRR002 Barrett's Adenocarcinoma 36 0.020
1179
SML032 Small Bowel Adenocarcinoma 36 0.020
1180
NNT008 Neonatal Abstinence Syndrome 35 0.020
1181
ULN001 Ulnar Neuropathy 35 0.020
1182
P ATR010 Atrial Heart Septal Defect 35 0.020
1183
AMY002 Amyloid Tumor 35 0.020
1184
HMR039 Hemorrhage, Intracerebral 35 0.020
1185
MNN017 Mononeuropathy 35 0.020
1186
ESP023 Esophageal Disease 34 0.020
1187
MYC015 Mycobacterium Fortuitum 34 0.020
1188
XRP001 Xerophthalmia 34 0.020
1189
P BLD036 Bile Duct Disease 34 0.020
1190
c HYP011 Hyperlipoproteinemia Type Iii 34 0.020
1191
TND006 Tendinosis 34 0.020
1192
PST053 Postherpetic Neuralgia 34 0.020
1193
CTN011 Cutaneous Porphyria 33 0.020
1194
HRT011 Heart Septal Defect 33 0.020
1195
BRN055 Bronchogenic Cyst 33 0.020
1196
RTN020 Retinal Vascular Disease 33 0.020
1197
CSL001 Causalgia 33 0.020
1198
PRM008 Parametritis 33 0.020
1199
PRN032 Paraneoplastic Cerebellar Degeneration 33 0.020
1200
BSL033 Basal Ganglia Cancification, Idiopathic, 1 32 0.020
1201
ANN005 Annular Pancreas 32 0.020
1202
TLS001 Tolosa-Hunt Syndrome 32 0.020
1203
IRR003 Irritant Dermatitis 32 0.020
1204
INS006 Insulin Autoimmune Syndrome 32 0.020
1205
P ATS061 Autosomal Recessive Hypotrichosis 32 0.020
1206
ADS002 Adie Syndrome 32 0.020
1207
MNN002 Mononeuritis Multiplex 31 0.020
1208
P OTT001 Otitis Externa 31 0.020
1209
IMR001 Imerslund-Grasbeck Syndrome 31 0.020
1210
ARB001 Ariboflavinosis 31 0.020
1211
PTT003 Pituitary-Dependent Cushing's Disease 31 0.020
1212
ENM001 Enamel Caries 31 0.020