Search results for Corticotropin

1098 hits were found for Corticotropin

# Family MCID Name MIFTS Score
1
P ACT092 Acth-Independent Macronodular Adrenal Hyperplasia 56 20.595
2
P ACT244 Acth-Independent Cushing Syndrome 38 10.772
3
ACT245 Acth-Dependent Cushing Syndrome 22 10.423
4
c ACT202 Acth-Independent Macronodular Adrenal Hyperplasia 2 34 9.600
5
CNN003 Conn's Syndrome 77 8.142
6
PTT037 Pituitary Tumors 44 5.782
7
ALC007 Alcohol Dependence 65 5.718
8
IRR002 Irritable Bowel Syndrome 64 5.543
9
MNT002 Mental Depression 56 5.409
10
ANX010 Anxiety 70 5.408
11
P MJR001 Major Depressive Disorder 68 5.194
12
P PTT006 Pituitary Adenoma 55 5.018
13
PST028 Post-Traumatic Stress Disorder 58 4.823
14
DPR016 Depression 64 4.752
15
ADN018 Adenoma 58 4.729
16
HYP056 Hypoglycemia 65 4.557
17
MDD011 Mood Disorder 61 4.339
18
P ALC033 Alcohol Use Disorder 67 4.212
19
P HYP083 Hypopituitarism 51 4.177
20
WST001 West Syndrome 64 3.901
21
ACT084 Acute Stress Disorder 53 3.863
22
P ART022 Arthritis 70 3.789
23
P NPH012 Nephrotic Syndrome 61 3.778
24
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 3.650
25
TXC005 Toxic Shock Syndrome 61 3.518
26
P SZR006 Seizure Disorder 69 3.377
27
HYP780 Hypoadrenocorticism, Familial 61 3.307
28
P RHM011 Rheumatoid Arthritis 81 3.295
29
P NRB001 Neuroblastoma 66 3.197
30
ANR007 Anorexia Nervosa 59 3.194
31
ALL029 Allergic Disease 61 3.153
32
END040 Endogenous Depression 54 3.124
33
P ACT010 Acth-Secreting Pituitary Adenoma 60 2.976
34
P PHC003 Pheochromocytoma 70 2.968
35
PRT037 Pertussis 49 2.966
36
P SBS003 Substance Abuse 54 2.912
37
CLT003 Colitis 63 2.901
38
ADR040 Adrenal Gland Pheochromocytoma 45 2.860
39
BRN004 Brain Edema 54 2.836
40
ULC004 Ulcerative Colitis 74 2.828
41
P PNC025 Panic Disorder 52 2.780
42
c SYS001 Systemic Lupus Erythematosus 85 2.679
43
P MYC033 Myoclonus 46 2.675
44
PTT009 Pituitary Gland Disease 52 2.671
45
ADR008 Adrenal Adenoma 55 2.655
46
P LPS004 Lupus Erythematosus 61 2.633
47
P MLT020 Multiple Sclerosis 79 2.609
48
c SCN052 Secondary Adrenal Insufficiency 35 2.584
49
OPS006 Opsoclonus-Myoclonus Syndrome 48 2.542
50
P UVT001 Uveitis 57 2.488
51
PRT251 Proteinuria, Chronic Benign 58 2.376
52
CHL014 Cholera 62 2.362
53
P SRC025 Sarcoidosis 1 70 2.362
54
CCN002 Cocaine Abuse 49 2.349
55
c PRC016 Pre-Eclampsia 64 2.312
56
PTT003 Pituitary-Dependent Cushing's Disease 39 2.258
57
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 2.218
58
c PRM093 Premature Ovarian Failure 7 47 2.214
59
ETN001 Eating Disorder 59 2.132
60
P DBT005 Diabetes Insipidus 54 2.117
61
P RTN024 Retinoblastoma 72 2.113
62
P DRM053 Dermatitis, Atopic 65 2.112
63
HYP266 Hypoxia 56 2.112
64
P PLY011 Polycystic Ovary Syndrome 57 2.102
65
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 2.097
66
c MJR022 Major Affective Disorder 8 37 2.094
67
c MJR024 Major Affective Disorder 9 40 2.094
68
P BPL003 Bipolar Disorder 56 2.094
69
48X005 48,xyyy 39 2.080
70
AMN001 Amenorrhea 53 2.074
71
BRN028 Brain Cancer 73 2.071
72
DRG003 Drug Dependence 46 2.059
73
c HYP795 Hypothyroidism, Congenital, Nongoitrous, 4 46 2.055
74
ACR007 Acromegaly 70 2.049
75
DRM006 Dermatitis 61 2.020
76
CCN001 Cocaine Dependence 47 2.017
77
AGN016 Aging 53 2.003
78
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.969
79
P HYP086 Hypothyroidism 68 1.962
80
WTH001 Withdrawal Disorder 47 1.935
81
PNG002 Pain Agnosia 51 1.931
82
FML063 Familial Glucocorticoid Deficiency 58 1.917
83
P THY032 Thyroiditis 56 1.916
84
P CYS018 Cystitis 58 1.907
85
CHR066 Chronic Fatigue Syndrome 59 1.902
86
P SML001 Small Cell Carcinoma 52 1.888
87
HYP005 Hypokalemia 55 1.886
88
PST021 Postpartum Depression 50 1.881
89
INS024 Insulin-Like Growth Factor I 77 1.863
90
CRC006 Carcinoid Syndrome 55 1.863
91
NRN004 Neuroendocrine Tumor 55 1.836
92
P CHR345 Chronic Pain 50 1.831
93
BRN053 Bronchial Adenomas/carcinoids Childhood 21 1.822
94
P MYS003 Myasthenia Gravis 67 1.807
95
ATM095 Autoimmune Disease 61 1.806
96
PPL052 Papillomatosis, Confluent and Reticulated 34 1.796
97
c DWL002 Dowling-Degos Disease 1 58 1.775
98
c PRM340 Primary Adrenal Insufficiency 37 1.766
99
PSR001 Psoriatic Arthritis 61 1.754
100
P ACN011 Acne 55 1.733
101
HYP060 Hyperinsulinism 53 1.731
102
THY029 Thyroid Carcinoma 55 1.730
103
SKN016 Skin Disease 63 1.720
104
LPD012 Lipoid Congenital Adrenal Hyperplasia 68 1.683
105
ILS001 Ileus 49 1.679
106
CYT002 Cytokine Deficiency 43 1.663
107
P INT143 Interstitial Cystitis 59 1.650
108
ANT039 Antisynthetase Syndrome 55 1.637
109
HYP705 Hyperadrenalism 24 1.637
111
P KDN018 Kidney Disease 71 1.637
112
CRC014 Carcinoid Tumors, Intestinal 46 1.629
113
HYP066 Hyperglycemia 60 1.602
114
P GLM040 Glioma Susceptibility 1 70 1.600
115
MLG169 Malignant Astrocytoma 57 1.600
116
HYP020 Hyperprolactinemia 63 1.578
117
P ALP008 Alopecia 53 1.574
118
RLP002 Relapsing-Remitting Multiple Sclerosis 56 1.569
119
CHL068 Cholestasis 61 1.561
120
c PGM022 Pigmented Nodular Adrenocortical Disease, Primary, 4 24 1.550
121
P ECL001 Eclampsia 52 1.549
122
THY111 Thyroid Carcinoma, Familial Medullary 67 1.509
123
THY125 Thyroid Gland Medullary Carcinoma 48 1.509
124
GLM045 Glioma 62 1.506
125
GLL048 Glial Tumor 51 1.506
126
c HYP595 Hypertension, Essential 84 1.494
127
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 55 1.479
128
P DRR001 Diarrhea 55 1.475
129
P MLT074 Multiple Endocrine Neoplasia 58 1.459
130
NRT004 Neuritis 53 1.445
131
PLY068 Polysubstance Abuse 41 1.428
132
P DRM010 Dermatomyositis 61 1.409
133
P SJG008 Sjogren Syndrome 60 1.403
134
TBC004 Tobacco Addiction 63 1.393
135
ALL014 Allergic Encephalomyelitis 34 1.392
136
PTT046 Pituitary Hormone Deficiency, Combined, 2 62 1.385
137
FBR047 Fibromyalgia 57 1.385
138
HYP043 Hyperandrogenism 47 1.379
139
P PLY041 Polymyositis 58 1.376
140
ISL001 Islet Cell Tumor 55 1.355
141
INS001 Insulinoma 59 1.355
142
GRW007 Growth Hormone Deficiency 47 1.355
143
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 1.355
144
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.355
145
P END044 Endometriosis 62 1.342
146
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 1.338
147
ZLL002 Zollinger-Ellison Syndrome 55 1.323
148
P ALZ034 Alzheimer Disease 87 1.313
149
ECT093 Ectopic Cushing Syndrome 45 1.313
150
P PRS038 Personality Disorder 65 1.313
151
PLC008 Placenta Disease 48 1.313
152
PPT005 Peptic Ulcer Disease 58 1.313
153
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 57 1.305
154
DRY001 Dry Eye Syndrome 49 1.305
155
KRT001 Keratoconjunctivitis Sicca 49 1.305
156
KRT006 Keratoconjunctivitis 53 1.305
157
CHR074 Choriocarcinoma 46 1.301
158
OBS002 Obsessive-Compulsive Disorder 67 1.300
159
PST011 Pustulosis of Palm and Sole 52 1.298
160
P PSR002 Psoriasis 63 1.298
161
TRM010 Traumatic Brain Injury 50 1.295
162
ADR041 Adrenal Cortical Adenoma 48 1.282
163
HLX001 Helix Syndrome 47 1.282
164
OPT003 Opiate Dependence 49 1.276
165
CNS004 Constipation 56 1.276
166
GNR004 Generalized Anxiety Disorder 54 1.276
167
BRN071 Brain Injury 50 1.266
168
P EXN002 Exanthem 58 1.251
170
RHM001 Rheumatic Fever 59 1.248
171
P PMP001 Pemphigus 54 1.248
172
P URT039 Urticaria 57 1.247
173
HYP080 Hypogonadism 49 1.239
174
MLN003 Melancholia 41 1.238
175
P MYP004 Myopathy 67 1.238
176
ACQ007 Acquired Immunodeficiency Syndrome 58 1.238
177
P TRM003 Tremor 50 1.238
178
OCL069 Ocular Motor Apraxia 57 1.224
179
P HYP076 Hyperthyroidism 53 1.224
180
PLM001 Pulmonary Tuberculosis 69 1.220
181
P PRG013 Paraganglioma 57 1.194
182
P OPT009 Optic Neuritis 57 1.180
183
P PNV001 Panuveitis 48 1.175
184
ADR005 Adrenal Carcinoma 58 1.170
185
IMM167 Immune Deficiency Disease 76 1.161
186
P DDN001 Duodenal Ulcer 52 1.161
187
CRB004 Cerebral Artery Occlusion 45 1.161
188
CNT047 Contact Dermatitis 56 1.157
189
HGH043 High Grade Glioma 46 1.151
190
ACT238 Acth Deficiency, Isolated 52 1.146
191
ATY001 Atypical Depressive Disorder 45 1.146
192
P SLP005 Sleep Disorder 61 1.146
193
P FCL005 Focal Segmental Glomerulosclerosis 57 1.143
194
VSC002 Vascular Dementia 59 1.143
195
DWR001 Dwarfism 44 1.143
196
P SMK004 Smoking As a Quantitative Trait Locus 3 44 1.133
197
NLS001 Nelson Syndrome 44 1.133
198
LPT014 Leptin Deficiency or Dysfunction 77 1.128
199
OPD006 Opioid Addiction 48 1.124
200
PTT057 Pituitary Adenoma 4, Acth-Secreting 49 1.118
201
NRT001 Neurotic Disorder 56 1.118
202
c PST005 Posterior Uveitis 54 1.110
203
P VSC011 Vasculitis 61 1.110
204
c MCR133 Microvascular Complications of Diabetes 4 41 1.100
205
c MCR113 Microvascular Complications of Diabetes 3 52 1.100
206
c MCR130 Microvascular Complications of Diabetes 6 41 1.100
207
c MCR120 Microvascular Complications of Diabetes 7 47 1.100
208
P MMB011 Membranous Nephropathy 50 1.100
209
P LTR001 Lateral Sclerosis 57 1.100
210
P FNG006 Feingold Syndrome 1 61 1.090
211
c SYS043 Systemic Lupus Erythematosus 1 38 1.090
212
PFF001 Pfeiffer Syndrome 77 1.085
213
CND002 Conduct Disorder 50 1.080
214
GST030 Gastrinoma 45 1.076
215
P HYP120 Hypoaldosteronism 33 1.076
216
BHR001 Behr Syndrome 51 1.067
217
P DYS193 Dystonia 11, Myoclonic 55 1.067
218
ADL002 Adult Syndrome 69 1.067
219
c ATS007 Autism Spectrum Disorder 71 1.064
220
SVR004 Severe Combined Immunodeficiency 70 1.060
221
c AMY091 Amyotrophic Lateral Sclerosis 1 87 1.059
222
P EYD002 Eye Disease 57 1.059
223
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.053
224
LWC001 Low Compliance Bladder 44 1.025
225
c BPL002 Bipolar I Disorder 47 1.025
226
ENT011 Enterocolitis 55 1.022
227
RTN001 Retinal Vasculitis 46 1.012
228
NRR001 Neuroretinitis 42 1.012
229
END057 Endometrial Cancer 76 1.006
230
P ESP024 Esophagitis 60 0.989
231
P HML002 Hemolytic Anemia 62 0.987
232
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.985
233
RBS001 Rabies 57 0.985
234
DFC004 Deficiency Anemia 74 0.981
235
KRT009 Keratosis 52 0.981
236
P INF037 Inflammatory Bowel Disease 53 0.979
237
P HNT016 Huntington Disease 73 0.979
238
GT001 Gout 63 0.979
239
P HYP730 Hypogonadotropic Hypogonadism 57 0.965
240
MRG013 Mirage Syndrome 44 0.964
241
P INT099 Intrahepatic Cholestasis of Pregnancy 61 0.961
242
END041 Endometrial Adenocarcinoma 63 0.961
243
BNS003 Binswanger's Disease 41 0.961
244
47X002 47,xyy 47 0.961
245
P HYP263 Hypersomnia 40 0.961
246
P GLM007 Glomerulonephritis 59 0.960
247
ADR016 Adrenal Cortical Carcinoma 61 0.951
248
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.951
249
P TBR001 Tuberous Sclerosis 69 0.951
250
ADR004 Adrenal Cortical Adenocarcinoma 38 0.951
251
P INF032 Infertility 60 0.951
252
LYM043 Lymphocytic Hypophysitis 31 0.951
253
MNN043 Meningioma, Familial 79 0.935
254
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.935
255
SCR001 Secretory Meningioma 40 0.935
256
INT395 Intracranial Meningioma 47 0.935
257
P MSC003 Muscular Atrophy 52 0.935
258
P HYP098 Hypereosinophilic Syndrome 66 0.935
259
P HRP006 Herpes Simplex 65 0.935
260
P CTN003 Cutaneous Lupus Erythematosus 52 0.935
261
PTT008 Pituitary Carcinoma 47 0.935
262
AVD001 Avoidant Personality Disorder 49 0.935
263
OLV001 Olivopontocerebellar Atrophy 50 0.935
264
P MNN013 Meningitis 65 0.935
265
GNT167 Genetic Obesity 33 0.935
266
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.919
267
PLY150 Polykaryocytosis Inducer 29 0.919
268
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.919
269
P ENC004 Encephalitis 61 0.919
270
HRN029 Hearing Loss, Noise-Induced 37 0.904
271
SYN007 Synovitis 54 0.904
272
PLC002 Plica Syndrome 35 0.904
273
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.903
274
P OST002 Osteoporosis 76 0.903
275
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.903
276
HSH003 Hashimoto Thyroiditis 60 0.903
277
c HYP836 Hypercholesterolemia, Familial, 1 73 0.903
278
EMP001 Empty Sella Syndrome 41 0.903
279
c SRC023 Sarcoidosis 2 44 0.899
280
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.885
281
MCC012 Mccune-Albright Syndrome 69 0.885
282
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.885
283
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.885
284
CHR005 Chorioamnionitis 50 0.885
285
STT001 Status Epilepticus 58 0.885
286
P KDN017 Kidney Cancer 60 0.885
287
HPT004 Hepatic Coma 43 0.885
288
P ALP009 Alopecia Areata 59 0.885
289
PMP006 Pemphigus Vulgaris, Familial 57 0.883
290
PRP030 Purpura 54 0.883
291
P EPL164 Epilepsy 70 0.874
292
P SCH015 Schizophrenia 74 0.865
293
P MJR007 Major Affective Disorder 1 42 0.865
294
P TMP001 Temporal Lobe Epilepsy 49 0.865
295
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.865
296
MRP001 Morphine Dependence 41 0.865
297
PSY004 Psychotic Disorder 66 0.865
298
GTR002 Goiter 52 0.865
299
HRP004 Herpes Zoster 60 0.863
300
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.844
301
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.844
302
c GRV008 Graves Disease 1 54 0.844
303
P ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 52 0.844
304
ANV001 Anovulation 46 0.844
305
GST050 Gastrointestinal System Disease 55 0.844
306
c ACT150 Acute Adrenal Insufficiency 48 0.835
307
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.821
308
GST023 Gastric Ulcer 52 0.821
309
P INT068 Intestinal Disease 53 0.821
310
P MYT002 Myotonic Dystrophy 51 0.821
311
SYN036 Syncope 44 0.821
312
HDN002 Head Injury 44 0.810
313
CRH001 Crohn's Disease 80 0.796
314
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.795
315
AND014 Androgenic Alopecia 46 0.795
316
P ALP061 Alopecia, Androgenetic, 1 48 0.795
317
P CLR023 Colorectal Cancer 100 0.795
318
CRV035 Cervical Cancer 72 0.795
319
LYM027 Lymphopenia 56 0.795
320
SBC016 Subacute Delirium 42 0.795
321
TBR011 Tuberculous Meningitis 48 0.795
322
SPN050 Spinocerebellar Degeneration 38 0.795
323
GLC106 Glucocorticoid Resistance, Generalized 47 0.782
324
GLC003 Glucose Intolerance 53 0.782
325
P RHN004 Rhinitis 56 0.768
326
P OBS001 Obstructive Jaundice 49 0.764
327
GRN017 Granulocytopenia 42 0.764
328
DNT005 Dentatorubral-Pallidoluysian Atrophy 59 0.763
329
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.763
330
P ASP006 Aspergillosis 71 0.763
331
c EPL073 Epilepsy, Nocturnal Frontal Lobe, 1 47 0.763
332
FCL012 Facial Paralysis 49 0.763
333
PLC001 Placenta Accreta 44 0.763
334
ANX004 Anoxia 40 0.763
335
LNP001 Loin Pain Hematuria Syndrome 17 0.763
336
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.753
337
IMP005 Impotence 52 0.753
338
CLL003 Cellulitis 53 0.753
339
P ADL010 Adult Respiratory Distress Syndrome 70 0.739
340
ALL003 Allergic Rhinitis 66 0.737
341
c MGR028 Migraine with or Without Aura 1 63 0.737
342
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 0.734
343
IRD001 Iridocyclitis 54 0.734
344
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.723
345
KRT071 Keratosis, Seborrheic 56 0.723
346
P SYS005 Systemic Scleroderma 73 0.723
347
ORC001 Orchitis 43 0.723
348
ALL010 Allergic Contact Dermatitis 55 0.723
349
c ACT073 Acute Leukemia 59 0.723
350
PMP014 Pemphigoid 48 0.723
351
INV005 Inverted Follicular Keratosis 31 0.723
352
PRT082 Preterm Premature Rupture of the Membranes 56 0.720
353
SXL003 Sexual Disorder 49 0.702
354
c TYP008 Type 1 Diabetes Mellitus 77 0.702
355
ATN005 Autonomic Dysfunction 45 0.702
356
PRN039 Paraneoplastic Syndromes 37 0.702
357
SPN186 Spinal Cord Injury 60 0.702
358
MYL080 Myalgic Encephalomyelitis/chronic Fatigue Syndrome 32 0.687
359
CRH005 Crohn's Colitis 53 0.682
360
ORL015 Oral Squamous Cell Carcinoma 43 0.682
361
P TMP003 Temporal Arteritis 68 0.682
362
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.682
363
HMF011 Hemifacial Spasm, Familial 33 0.682
364
P BLP003 Blepharospasm 45 0.682
365
P MST009 Mastocytosis 64 0.682
366
PRM020 Premenstrual Tension 39 0.682
367
P NRP001 Neuropathy 59 0.682
368
PRM331 Primary Hypophysitis 18 0.682
369
P HMF004 Hemifacial Spasm 38 0.682
370
MTB004 Metabolic Acidosis 48 0.661
371
P HYP750 Hypertriglyceridemia, Familial 61 0.661
372
c ATR087 Atrial Standstill 1 74 0.661
373
SQM006 Squamous Cell Carcinoma 59 0.661
374
PNC027 Pancreatic Gastrinoma 30 0.661
375
AGR002 Agoraphobia 45 0.661
376
P HYP077 Hypertrichosis 48 0.661
377
URM002 Uremia 47 0.661
378
SCL003 Social Phobia 48 0.661
379
PTT004 Pituitary Apoplexy 46 0.661
380
DYS009 Dysthymic Disorder 51 0.661
381
ALD013 Aldosterone-Producing Adenoma 36 0.661
382
P ENC018 Encephalopathy 62 0.661
383
P TRN020 Turner Syndrome 67 0.646
384
NTR005 Nutritional Deficiency Disease 60 0.646
385
PTH003 Pathologic Nystagmus 52 0.646
386
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.638
387
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.638
388
GST092 Gastroesophageal Reflux 59 0.638
389
P GST053 Gastric Cancer 82 0.638
390
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.638
391
DPH001 Diphtheria 59 0.638
392
c CHR708 Chronic Urticaria 42 0.638
393
P ART021 Arteriosclerosis 53 0.638
394
GNG005 Gangliocytoma 54 0.638
395
P PNM007 Pneumonia 64 0.638
396
P OVR049 Ovarian Disease 50 0.638
397
P LVR013 Liver Disease 68 0.638
398
P GST044 Gastritis 55 0.638
399
P BRS044 Breast Adenocarcinoma 58 0.638
400
BRD004 Borderline Personality Disorder 53 0.638
401
P MLN008 Melanoma 75 0.638
402
BRN056 Bronchopulmonary Dysplasia 57 0.638
403
FST010 Fasting Hypoglycemia 33 0.638
404
c NRB010 Neuroblastoma 1 59 0.626
405
ERY003 Erythema Multiforme 56 0.624
406
CFF003 Caffey Disease 53 0.624
407
RTC012 Reticuloendotheliosis, X-Linked 35 0.624
408
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.624
409
OCL051 Ocular Tuberculosis 29 0.624
410
HYP068 Hyperostosis 47 0.624
411
P GLL022 Guillain-Barre Syndrome 59 0.624
412
ACQ008 Acquired Hyperkeratosis 21 0.624
413
P CLL015 Collagen Disease 47 0.624
414
TRC023 Trichinosis 53 0.624
415
HRP011 Herpes Zoster Ophthalmicus 24 0.624
416
c MCR115 Microvascular Complications of Diabetes 5 65 0.618
417
P CRN300 Coronary Heart Disease 1 73 0.612
418
ECT026 Ectopic Pregnancy 47 0.612
419
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.612
420
P MDL005 Medulloblastoma 75 0.612
421
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.612
422
STR067 Stroke, Ischemic 79 0.612
423
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.612
424
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.612
425
c PTT061 Pituitary Adenoma 3, Multiple Types 32 0.612
426
CYC008 Cyclic Vomiting Syndrome 46 0.612
427
c PNC068 Panic Disorder 3 12 0.612
428
P TCD001 Tic Disorder 50 0.612
429
BCT002 Bacterial Vaginosis 52 0.612
430
SXC001 Sex Cord-Gonadal Stromal Tumor 47 0.612
431
HYP085 Hypothalamic Disease 38 0.612
432
P PRP019 Peripheral Nervous System Disease 57 0.612
433
ENT004 Enthesopathy 51 0.612
434
CHR034 Chromophobe Adenoma 35 0.612
435
P HYP061 Hypertrophic Cardiomyopathy 68 0.612
436
SCH014 Schistosomiasis 56 0.612
437
ACT038 Acute Retrobulbar Neuritis 25 0.612
438
NRN001 Neuroendocrine Carcinoma 47 0.612
439
P CTR002 Cataract 59 0.612
440
CHL061 Childhood Leukemia 47 0.612
441
SBS004 Substance Dependence 46 0.612
442
P MSC005 Muscular Dystrophy 66 0.612
443
HYP855 Hyperpigmentation of the Skin 25 0.612
444
P PRD021 Periodic Paralysis 42 0.612
445
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 0.581
446
P BLD134 Bladder Cancer 79 0.581
447
P SPP010 Suppressor of Tumorigenicity 3 50 0.581
448
GLC042 Glucocorticoid Deficiency 1 49 0.581
449
P GRF003 Graft-Versus-Host Disease 71 0.581
450
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.581
451
P MYS005 Myositis 55 0.581
452
HMN044 Human Immunodeficiency Virus Type 1 76 0.581
453
PRS129 Prostatic Hyperplasia, Benign 48 0.581
454
BCT021 Bacterial Sepsis 43 0.581
455
THY128 Thyroid Tumor 33 0.581
456
BNR002 Bone Resorption Disease 47 0.581
457
INP001 Inappropriate Adh Syndrome 48 0.581
458
CRB037 Cerebral Palsy 66 0.581
459
EXT054 Extra-Adrenal Pheochromocytoma 31 0.581
460
ACD008 Acid-Labile Subunit Deficiency 52 0.581
461
PLM012 Pulmonary Sarcoidosis 52 0.581
462
P BNG030 Benign Ependymoma 51 0.581
463
MLT001 Multiple Chemical Sensitivity 38 0.581
464
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.581
465
CLL010 Cellular Ependymoma 58 0.581
466
MSN004 Mesenchymal Cell Neoplasm 42 0.581
467
NPH009 Nephrolithiasis 54 0.581
468
OVR063 Overnutrition 42 0.581
469
GST045 Gastroenteritis 58 0.581
470
NWC001 Newcastle Disease 47 0.581
471
GNG008 Ganglioneuroblastoma 46 0.581
472
PRS021 Prostatic Adenoma 43 0.581
473
PLS011 Plasmacytoma 56 0.581
474
OST011 Osteomalacia 52 0.581
475
RCK004 Rickets 64 0.581
476
PRS045 Prostatic Hypertrophy 53 0.581
477
SCH011 Schizotypal Personality Disorder 36 0.581
478
CHG001 Chagas Disease 65 0.581
479
c SVR005 Severe Pre-Eclampsia 49 0.581
480
ACH005 Achalasia 54 0.581
481
P LCH002 Lichen Planus 54 0.581
482
FSC004 Fasciitis 49 0.581
483
P MYC008 Myocarditis 59 0.581
484
PRT036 Peritonitis 65 0.581
485
SHH001 Sheehan Syndrome 45 0.581
486
P TXP001 Toxoplasmosis 59 0.581
487
ESN002 Eosinophilia-Myalgia Syndrome 40 0.581
488
HYP231 Hypothalamic Hamartomas 33 0.581
489
P PLY017 Polyarteritis Nodosa 59 0.581
490
P ACT105 Acute Mountain Sickness 52 0.581
491
P FBR031 Febrile Seizures 52 0.581
492
c SPN225 Spondyloarthropathy 1 70 0.571
493
MXD026 Mixed Glioma 45 0.571
494
RTN023 Retinitis 45 0.571
495
AND005 Androgen Insensitivity Syndrome, Mild 21 0.571
496
P ANR048 Aniridia 1 66 0.548
497
MCS002 Mucositis 55 0.548
498
FNC007 Functioning Pituitary Adenoma 42 0.548
499
P CRV039 Cervicitis 52 0.548
500
PPL001 Papillary Adenoma 44 0.548
501
CRB009 Cerebritis 43 0.548
502
DYS011 Dyskinesia of Esophagus 41 0.548
503
c PRM038 Primary Agammaglobulinemia 47 0.548
504
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 0.540
505
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.540
506
CRB028 Cerebellar Medulloblastoma 33 0.540
507
RNL077 Renal Fibrosis 46 0.540
508
c PRG020 Paragangliomas 3 39 0.540
509
c WLM013 Wilms Tumor 1 65 0.540
510
CYS001 Cystic Fibrosis 77 0.540
511
HYP052 Hyperkalemic Periodic Paralysis 62 0.540
512
CRD132 Cardiac Conduction Defect 59 0.540
513
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.540
514
c PNS012 Paine Syndrome 60 0.540
515
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.540
516
PRP027 Peripheral Vascular Disease 71 0.540
517
c INF002 Inflammatory Diarrhea 30 0.540
518
ASP026 Asplenia, Isolated Congenital 43 0.540
519
c THY107 Thymoma, Familial 42 0.540
520
ALP097 Alopecia Universalis Congenita 57 0.540
521
KRT019 Keratitis, Hereditary 66 0.540
522
c HMC039 Hemochromatosis, Type 1 73 0.540
523
SPN392 Spondylosis, Cervical 30 0.540
524
DBT087 Diabetes Insipidus, Neurohypophyseal 58 0.540
525
P MMP001 Mumps 56 0.540
526
PRS064 Persistent Vegetative State 33 0.540
527
SCH003 Schizophreniform Disorder 54 0.540
528
P PRK039 Parkinsonism 55 0.540
529
CLR109 Colorectal Adenocarcinoma 50 0.540
530
PLC006 Placental Choriocarcinoma 38 0.540
531
SPN020 Spondylosis 46 0.540
532
P THY023 Thymoma 64 0.540
533
SCK001 Sick Building Syndrome 33 0.540
534
c BSL007 Basal Cell Carcinoma 67 0.540
535
c ACT071 Acute Kidney Failure 60 0.540
536
P GLY013 Glycogen Storage Disease 59 0.540
537
CRB027 Cerebellar Disease 47 0.540
538
P VSC007 Vascular Disease 62 0.540
539
P BNC003 Bone Cancer 58 0.540
540
ADJ001 Adjustment Disorder 46 0.540
541
CLR030 Clear Cell Renal Cell Carcinoma 53 0.540
542
PRP016 Paraplegia 52 0.540
543
LNG020 Lung Oat Cell Carcinoma 51 0.540
544
ACT098 Acute Erythroid Leukemia 55 0.540
545
HMP005 Hemiplegia 53 0.540
546
c FML021 Familial Hypercholesterolemia 71 0.540
547
MNC001 Monocular Esotropia 30 0.540
548
TYP007 Typhoid Fever 63 0.540
549
P NRM002 Normal Pressure Hydrocephalus 49 0.540
550
TST015 Testicular Disease 42 0.540
551
TRT001 Teratocarcinoma 41 0.540
552
P SKN015 Skin Carcinoma 71 0.540
553
GST010 Gestational Trophoblastic Neoplasm 52 0.540
554
MCR013 Microphthalmia 59 0.540
555
P HYD006 Hydrocephalus 62 0.540
556
PLP001 Pulpitis 48 0.540
557
VRC001 Varicocele 48 0.540
558
SHG001 Shigellosis 61 0.540
559
PHB001 Phobic Disorder 45 0.540
560
OCL010 Ocular Hypotension 37 0.540
561
P OVR046 Ovarian Cyst 43 0.540
562
HYP034 Hypertensive Encephalopathy 43 0.540
563
CRV002 Cervix Uteri Carcinoma in Situ 48 0.540
564
ACT058 Active Peptic Ulcer Disease 55 0.540
565
MSL001 Measles 61 0.540
566
PRN019 Perinatal Necrotizing Enterocolitis 60 0.540
567
ATM061 Autoimmune Polyglandular Syndrome Type 3 28 0.540
568
c SBC007 Subacute Thyroiditis 43 0.540
569
P VSC018 Visceral Steatosis 32 0.540
570
P AMY004 Amyloidosis 69 0.540
571
c BCT013 Bacterial Pneumonia 47 0.540
572
CRV045 Cervical Intraepithelial Neoplasia 38 0.540
573
INT075 Intracranial Hypertension 52 0.540
574
ORG003 Organic Mood Syndrome 13 0.540
575
EST005 Esotropia 43 0.540
576
DMN012 Dementia - Subcortical 17 0.540
577
P PLY014 Polycystic Kidney Disease 71 0.532
578
P MCR129 Microvascular Complications of Diabetes 1 67 0.519
579
VSL013 Visual Impairment and Progressive Phthisis Bulbi 36 0.519
580
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 49 0.519
581
c MCR112 Microvascular Complications of Diabetes 2 42 0.519
582
RSP019 Respiratory Distress Syndrome in Premature Infants 52 0.519
583
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 0.519
584
c PRM092 Primary Lateral Sclerosis, Adult, 1 38 0.519
585
INT002 Intermittent Claudication 61 0.519
586
P MTR014 Motor Neuron Disease 65 0.519
587
VSL002 Visual Epilepsy 39 0.519
588
NWB001 Newborn Respiratory Distress Syndrome 56 0.519
589
ATX019 Ataxia with Vitamin E Deficiency 44 0.519
590
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.519
591
RSP007 Respiratory Distress Syndrome, Infant 41 0.519
592
LNG108 Langerhans Cell Histiocytosis 57 0.441
593
P APL001 Aplastic Anemia 72 0.441
594
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.441
595
PRP069 Purpura Simplex 16 0.441
596
ATH013 Atherosclerosis Susceptibility 63 0.441
597
FLT011 Felty Syndrome 51 0.441
598
FBR011 Fibrodysplasia Ossificans Progressiva 67 0.441
599
P PTY003 Pityriasis Rubra Pilaris 57 0.441
600
HYP611 Hypoparathyroidism, X-Linked 29 0.441
601
c CNG006 Congenital Hypothyroidism 63 0.441
602
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 0.441
603
LRY004 Laryngotracheitis 32 0.441
604
PRP083 Porphyria, Acute Intermittent 64 0.441
605
P LPR021 Leprosy 3 71 0.441
606
P MYC084 Mycobacterium Tuberculosis 1 68 0.441
608
SVR097 Severe Cutaneous Adverse Reaction 68 0.441
609
OCL020 Ocular Cicatricial Pemphigoid 52 0.441
610
RSP021 Respiratory Allergy 41 0.441
611
c INF151 Infectious Panuveitis 13 0.441
612
THR024 Thrombosis 56 0.441
613
CCT002 Cicatricial Pemphigoid 53 0.441
614
ACT029 Acute Interstitial Pneumonia 49 0.441
615
HST010 Histiocytosis 49 0.441
616
RTN020 Retinal Vascular Disease 45 0.441
617
CLC006 Calcinosis 47 0.441
618
P OTS001 Otosclerosis 49 0.441
619
P PLY020 Polyradiculoneuropathy 47 0.441
620
LPT001 Leptospirosis 65 0.441
621
FRZ001 Frozen Shoulder 54 0.441
622
c ACT053 Acute Thyroiditis 29 0.441
623
P MYP006 Myopia 55 0.441
624
MDD018 Middle East Respiratory Syndrome 44 0.441
625
PNC008 Pancreatic Endocrine Carcinoma 39 0.441
626
P PRP029 Porphyria 60 0.441
627
P PLY019 Polyneuropathy 52 0.441
628
P AGM001 Agammaglobulinemia 67 0.441
629
MYM001 Myoma 54 0.441
630
RHS001 Rh Isoimmunization 29 0.441
631
P LPM005 Lipomatosis 47 0.441
632
NRD001 Neurodermatitis 39 0.441
633
BNN003 Bone Inflammation Disease 47 0.441
634
BRS064 Bursitis 51 0.441
635
SYM002 Sympathetic Ophthalmia 45 0.441
636
CRN017 Coronary Thrombosis 46 0.441
637
THY001 Thyroid Crisis 30 0.441
638
CHR073 Choreatic Disease 53 0.441
639
CHL028 Childhood Type Dermatomyositis 58 0.441
640
CHR051 Chorea Gravidarum 21 0.441
641
DMP001 Dumping Syndrome 43 0.441
642
CHL004 Cholelithiasis 48 0.441
643
HMG002 Hemoglobinuria 50 0.441
644
MYS001 Myositis Ossificans 44 0.441
645
c JVN010 Juvenile Rheumatoid Arthritis 52 0.441
646
PNC019 Pancreatoblastoma 40 0.441
647
PTY002 Pityriasis Versicolor 38 0.441
648
ACT094 Acute Articular Rheumatism 24 0.441
649
DRM011 Dermatophytosis 52 0.441
650
PRP005 Parapsoriasis 38 0.441
651
END086 End Stage Renal Disease 54 0.441
652
HNS001 Hansen's Disease 32 0.441
653
GST039 Gastroduodenitis 37 0.441
654
PST053 Postherpetic Neuralgia 39 0.441
656
EXP004 Exophthalmos 50 0.441
657
INT065 Interstitial Keratitis 31 0.441
658
ACT228 Acute Radiation Syndrome 30 0.441
659
ERY066 Erythema Multiforme Major 29 0.441
660
FBR085 Fibrillary Glomerulonephritis 25 0.441
661
CRC034 Carcinoma Showing Thymus-Like Differentiation 22 0.441
662
CRB090 Cerebral Hypoxia 42 0.441
663
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 0.441
664
P CRN038 Carney Complex Variant 63 0.381
665
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.381
666
RNL065 Renal Cell Carcinoma, Papillary, 1 79 0.361
667
CHR177 Chromophobe Renal Cell Carcinoma 54 0.361
668
HPT070 Hepatosplenic T-Cell Lymphoma 35 0.361
669
P CRD119 Cardiac Arrest 68 0.355
670
P ATS364 Autism 72 0.355
671
P PRC019 Precocious Puberty 48 0.355
672
c TYP009 Type 2 Diabetes Mellitus 91 0.341
673
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.341
674
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.341
675
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.341
676
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.341
677
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.341
678
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.341
679
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.341
680
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.341
681
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.341
682
LVR012 Liver Cirrhosis 62 0.341
683
INF021 Infant Gynecomastia 30 0.295
684
CRN036 Craniopharyngioma 63 0.295
685
GYN001 Gynecomastia 48 0.295
686
BLM002 Bulimia Nervosa 56 0.278
687
LPD008 Lipid Metabolism Disorder 61 0.278
688
P NRC002 Narcolepsy 55 0.278
689
P SLP006 Sleep Apnea 69 0.260
690
c HYP731 Hyperaldosteronism, Familial, Type I 59 0.260
691
P AST005 Asthma 75 0.260
692
HPT019 Hepatic Encephalopathy 59 0.260
693
DMY004 Demyelinating Disease 50 0.260
694
CRD137 Cardiogenic Shock 56 0.260
695
CYN002 Cyanosis, Transient Neonatal 43 0.241
696
IGR001 Ige Responsiveness, Atopic 58 0.241
697
CNG034 Congestive Heart Failure 69 0.241
698
PLM013 Pulmonary Immaturity 31 0.241
699
c ACT027 Acute Pancreatitis 60 0.241
700
3BT001 3-Beta-Hydroxysteroid Dehydrogenase Deficiency 40 0.241
701
P DBT009 Diabetes Mellitus 67 0.241
702
P PRD006 Prader-Willi Syndrome 60 0.220
703
PRT010 Parathyroid Carcinoma 68 0.220
704
P RSP003 Respiratory Failure 73 0.220
705
P PNC044 Pancreatitis 61 0.220
706
PRT058 Pure Autonomic Failure 58 0.220
707
c CNT075 Central Precocious Puberty 53 0.220
708
HYP835 Hypothalamic Obesity 38 0.220
709
APH002 Aphasia 55 0.197
710
LNN001 Lennox-Gastaut Syndrome 61 0.197
711
GLC096 Galactorrhea 40 0.197
712
c GLL024 Gallbladder Disease 1 53 0.197
713
P PRK057 Parkinson Disease, Late-Onset 79 0.197
714
P HPT023 Hepatocellular Carcinoma 95 0.197
715
P HMN010 Hemangioma 61 0.197
716
FDL002 Food Allergy 47 0.197
717
BCT022 Bacterial Infectious Disease 55 0.197
718
ISC004 Ischemia 61 0.197
719
P CRD246 Cardiovascular System Disease 55 0.197
720
c ACT075 Acute Myocardial Infarction 55 0.197
721
P BCL017 B-Cell Lymphoma 57 0.197
722
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 0.170
723
c PRM108 Primary Progressive Multiple Sclerosis 51 0.170
724
HYP784 Hypogonadism, Male 43 0.170
725
MSC157 Muscular Dystrophy, Duchenne Type 78 0.170
726
P RTT002 Rett Syndrome 79 0.170
727
OST159 Osteogenic Sarcoma 66 0.170
728
P NSP012 Nasopharyngeal Carcinoma 60 0.170
729
P LKM062 Leukemia, Acute Lymphoblastic 69 0.170
730
P MYC007 Myocardial Infarction 69 0.170
731
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.170
732
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.170
733
NTR018 Neutrophilia, Hereditary 49 0.170
734
LNT004 Lentigines 45 0.170
735
WST005 West Nile Virus 55 0.170
736
ISL003 Isolated Growth Hormone Deficiency 56 0.170
737
TRY001 Trypanosomiasis 50 0.170
738
BRN012 Bronchiolitis Obliterans 56 0.170
739
MYF002 Myofascial Pain Syndrome 46 0.170
740
HPT014 Hepatorenal Syndrome 49 0.170
741
BRN002 Bronchiolitis 57 0.170
742
MNN009 Meningoencephalitis 47 0.170
743
MST005 Mastitis 52 0.170
744
OLF005 Olfactory Neuroblastoma 46 0.170
745
ALL006 Allergic Asthma 55 0.170
746
ADR022 Adrenomyeloneuropathy 38 0.170
747
YLL002 Yellow Fever 61 0.170
748
OST012 Osteoarthritis 77 0.170
749
LNG099 Lung Disease 62 0.170
750
PTC005 Pituicytoma 28 0.170
751
ADN064 Adenohypophysitis 34 0.170
752
WST010 West Nile Virus Infection 32 0.170
753
P DYS021 Dysautonomia 38 0.170
754
PST092 Posttransplant Acute Limbic Encephalitis 29 0.170
755
c MLT160 Multiple Endocrine Neoplasia, Type Iia 67 0.139
756
OPT070 Optic Nerve Hypoplasia, Bilateral 55 0.139
757
P OVR042 Ovarian Cancer 88 0.139
758
CLB010 Coloboma of Macula 53 0.139
759
SPT006 Septooptic Dysplasia 62 0.139
760
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.139
761
ADR007 Adrenoleukodystrophy 73 0.139
762
SPP011 Suppression of Tumorigenicity 12 61 0.139
763
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.139
764
ANN002 Anencephaly 57 0.139
765
APP015 Apparent Mineralocorticoid Excess 57 0.139
766
c TBR025 Tuberous Sclerosis 1 84 0.139
767
KLD003 Keloid Formation 34 0.139
768
PPL058 Papilloma of Choroid Plexus 54 0.139
769
c 46X049 46,xy Sex Reversal 2 51 0.139
770
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.139
771
P LKM071 Leukemia, Chronic Lymphocytic 74 0.139
772
MLT157 Multiple System Atrophy 1 69 0.139
773
OBS081 Obesity, Early-Onset, with Adrenal Insufficiency and Red Hair 37 0.139
774
P FTL002 Fatal Familial Insomnia 50 0.139
775
ADN027 Adenomyosis 59 0.139
776
PHY002 Physical Disorder 40 0.139
777
OPD001 Opioid Abuse 44 0.139
778
FML035 Familial Hyperlipidemia 54 0.139
779
P HYP069 Hyperparathyroidism 62 0.139
780
FCL014 Focal Epilepsy 53 0.139
781
PPL002 Papillary Carcinoma 46 0.139
782
VCC001 Vaccinia 49 0.139
783
BLR008 Bilirubin Metabolic Disorder 57 0.139
784
PPL022 Papilloma 53 0.139
785
P BNG032 Benign Mesothelioma 53 0.139
786
HMS001 Hemosiderosis 48 0.139
787
CRT020 Cortisone Reductase Deficiency 36 0.139
788
FLL031 Follicular Adenoma 40 0.139
789
P GRW001 Growth Hormone Secreting Pituitary Adenoma 47 0.139
790
P DYS154 Dystonia 64 0.139
791
GST037 Gastroparesis 52 0.139
792
SMT001 Somatization Disorder 49 0.139
793
SQM002 Squamous Cell Papilloma 45 0.139
794
LYD001 Leydig Cell Tumor 45 0.139
795
P ADN016 Adenocarcinoma 63 0.139
796
THY030 Thyroid Gland Disease 50 0.139
797
P PLM036 Pulmonary Fibrosis 65 0.139
798
P TRT010 Teratoma 50 0.139
799
ATN004 Autonomic Neuropathy 42 0.139
800
P HYP024 Hypoparathyroidism 55 0.139
801
c PRM005 Primary Hyperparathyroidism 59 0.139
802
PRC002 Paracoccidioidomycosis 53 0.139
803
PRM013 Premature Menopause 57 0.139
804
P MCR010 Microcephaly 59 0.139
805
PCD001 Pica Disease 38 0.139
806
OLG003 Oligohydramnios 50 0.139
807
P NTR004 Neutropenia 62 0.139
808
OLG001 Oligospermia 45 0.139
809
EST004 Estrogen Excess 37 0.139
810
P DMN002 Dementia 65 0.139
811
SLP001 Sleeping Sickness 56 0.139
812
c VRL007 Viral Encephalitis 50 0.139
813
P PRN023 Prion Disease 60 0.139
814
PNC016 Pancreatic Cholera 32 0.139
815
PRT029 Parathyroid Adenoma 51 0.139
816
LRN003 Learning Disability 49 0.139
817
KLD004 Keloid Disorder 38 0.139
819
P BRN022 Bronchiectasis 59 0.139
820
PTT001 Pituitary Hypoplasia 34 0.139
821
P RTN016 Retinal Degeneration 52 0.139
822
P CLS010 Cluster Headache 42 0.139
823
DBT010 Diabetic Neuropathy 54 0.139
824
MLG079 Malignant Pleural Mesothelioma 42 0.139
825
HRP009 Herpes Simplex Encephalitis 58 0.139
826
P THL005 Thalassemia 56 0.139
827
BCK006 Back Pain 43 0.139
828
P OTT001 Otitis Externa 43 0.139
829
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.139
830
PTT041 Pituitary Stalk Interruption Syndrome 54 0.139
831
c ATM075 Autoimmune Encephalitis 39 0.139
832
P RRH023 Rare Hereditary Hemochromatosis 52 0.139
833
THY108 Thymic Neuroendocrine Tumor 32 0.139
834
P RRT020 Rare Tumor 39 0.139
835
P HYP265 Hypotonia 42 0.139
836
P HDC001 Headache 56 0.139
837
ADR057 Adrenogenital Syndrome 31 0.139
838
MSC193 Muscular Lipidosis 23 0.139
839
BLT017 Bilateral Massive Adrenal Hemorrhage 17 0.139
840
P OVR082 Overgrowth Syndrome 41 0.139
841
APR001 Apraxia 51 0.098
842
ADT001 Auditory Agnosia 25 0.098
843
VRB001 Verbal Auditory Agnosia 18 0.098
844
ISC015 Ischemic Colitis 43 0.098
845
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.098
846
c PGM021 Pigmented Nodular Adrenocortical Disease, Primary, 1 29 0.098
847
c MLT086 Multiple Endocrine Neoplasia, Type Iv 51 0.098
849
ALX002 Alexithymia 36 0.098
850
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.098
851
SGM008 Segmental Dystonia 28 0.098
852
P LYM118 Lymphoma 66 0.098
853
ILC002 Ileocolitis 42 0.098
854
DCT002 Ductal Carcinoma in Situ 58 0.098
855
P CLC063 Celiac Disease 1 65 0.098
856
CRP032 Corpus Callosum, Agenesis of 49 0.098
857
VRC005 Varicose Veins 59 0.098
858
WLL001 Williams-Beuren Syndrome 60 0.098
859
c CRN243 Carney Complex, Type 1 53 0.098
860
TRT017 Teratoma, Ovarian 28 0.098
861
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.098
862
P PRS040 Prostate Cancer 95 0.098
863
c SCL052 Scleroderma, Familial Progressive 60 0.098
864
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.098
865
c SML038 Small Cell Cancer of the Lung 68 0.098
866
GLL008 Gilles De La Tourette Syndrome 64 0.098
867
c GLC092 Glaucoma, Primary Open Angle 60 0.098
868
HND015 Hand Skill, Relative 29 0.098
869
SMT008 Smith-Magenis Syndrome 53 0.098
870
EPP024 Epiphyseal Dysplasia, Multiple, with Early-Onset Diabetes Mellitus 55 0.098
871
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 49 0.098
872
P PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 66 0.098
873
17B003 17-Beta Hydroxysteroid Dehydrogenase Iii Deficiency 37 0.098
874
c OPT051 Opitz Gbbb Syndrome, Type I 45 0.098
875
EXT059 External Auditory Canal, Bilateral Atresia of, with Congenital Vertical Talus 27 0.098
876
c EXD008 Exudative Vitreoretinopathy 1 71 0.098
877
c ALZ050 Alzheimer Disease 5 35 0.098
878
CRB081 Cerebellar Ataxia, Cayman Type 39 0.098
879
c DRM040 Dermatitis Herpetiformis, Familial 35 0.098
880
MLG141 Malignant Atrophic Papulosis 35 0.098
881
c SCH084 Schizophrenia 8 27 0.098
882
HMC014 Homocysteinemia 52 0.098
883
SCH018 Schizencephaly 52 0.098
884
CHR387 Chromosome Xp21 Deletion Syndrome 36 0.098
885
CNG184 Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects 56 0.098
886
DRV001 Dravet Syndrome 69 0.098
887
EPL050 Epilepsy, Partial, with Pericentral Spikes 26 0.098
888
RST023 Resting Heart Rate, Variation in 40 0.098
889
PLY183 Polymicrogyria with or Without Vascular-Type Ehlers-Danlos Syndrome 41 0.098
890
LPP008 Lipoprotein Quantitative Trait Locus 65 0.098
891
TND005 Tendinitis 53 0.098
892
DSS032 Disease by Infectious Agent 55 0.098
893
HYP017 Hypophosphatemia 49 0.098
894
P RST001 Restless Legs Syndrome 52 0.098
895
ATS010 Autosomal Recessive Disease 42 0.098
896
c HPT073 Hepatitis C Virus 70 0.098
897
P HGH038 High Density Lipoprotein Cholesterol Level Quantitative Trait Locus 6 12 0.098
898
PRC054 Perching Syndrome 32 0.098
899
P PLM037 Pulmonary Hypertension 69 0.098
900
ARM001 Aromatase Deficiency 54 0.098
901
MSC007 Muscle Hypertrophy 64 0.098
902
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.098
903
HYP110 Hyperproinsulinemia 37 0.098
904
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 50 0.098
905
c ACT004 Acute Diarrhea 40 0.098
906
P ERL057 Early Infantile Epileptic Encephalopathy 61 0.098
907
c RHB023 Rhabdomyosarcoma, Embryonal, 1 44 0.098
908
GLY014 Glycerol Kinase Deficiency 48 0.098
909
P CHN012 Chondrosarcoma 56 0.098
910
P LNG032 Lung Cancer 98 0.098
911
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 58 0.098
912
c PLY137 Polydactyly, Preaxial Iii 21 0.098
913
INT303 Intracranial Hypertension, Idiopathic 56 0.098
914
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 67 0.098
915
CHY002 Chylomicron Retention Disease 64 0.098
916
SMT004 Smith-Lemli-Opitz Syndrome 69 0.098
917
SDD001 Sudden Infant Death Syndrome 60 0.098
918
THY039 Thyrotropin-Releasing Hormone Deficiency 28 0.098
919
CHR525 Chromosome Xq26.3 Duplication Syndrome 36 0.098
920
P STR020 Strabismus 56 0.098
921
c TBR026 Tuberous Sclerosis 2 71 0.098
922
ALP103 Alpha-1-Antitrypsin Deficiency 67 0.098
923
c DYS151 Dystonia 25 41 0.098
924
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.098
925
SCH071 Schaaf-Yang Syndrome 53 0.098
926
c LKM063 Leukemia, Chronic Myeloid 70 0.098
927
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.098
928
P TMR010 Tumor Predisposition Syndrome 69 0.098
929
KWS002 Kawasaki Disease 65 0.098
930
ABD009 Abducens Palsy 23 0.098
931
ACN002 Acanthosis Nigricans 56 0.098
932
MTP034 Metaphyseal Chondrodysplasia, Jansen Type 50 0.098
933
ARM004 Aromatase Excess Syndrome 52 0.098
934
MST024 Mastocytosis, Cutaneous 66 0.098
935
MTN003 Motion Sickness 50 0.098
936
c NPH049 Nephrotic Syndrome, Type 2 49 0.098
937
P ORT004 Orthostatic Intolerance 61 0.098
938
P EPL140 Epilepsy, Idiopathic Generalized 60 0.098
939
P BND020 Bone Disease 60 0.098
940
FBR009 Fibrous Dysplasia 48 0.098
941
DFF005 Diffuse Large B-Cell Lymphoma 55 0.098
942
P LYM033 Lymphoproliferative Syndrome 59 0.098
943
XLN228 X-Linked Recessive Disease 24 0.098
944
HRT040 Hirata Disease 39 0.098
945
CMB007 Combined Immunodeficiency 56 0.098
946
P SNS001 Sensorineural Hearing Loss 60 0.098
947
OST017 Osteomyelitis 63 0.098
948
THY092 Thymic Neuroendocrine Carcinoma 14 0.098
949
HMN048 Human Papillomavirus Infectious Disease 45 0.098
950
DSS009 Disseminated Intravascular Coagulation 56 0.098
951
CHL123 Chlamydia 58 0.098
952