Search results for crh

700 hits were found for crh

# Family MCID Name MIFTS Score
1
P ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 52 27.748
2
CNN003 Conn's Syndrome 77 19.113
3
P MJR001 Major Depressive Disorder 68 17.931
4
DPR016 Depression 65 15.890
5
HYP056 Hypoglycemia 65 15.226
6
MDD011 Mood Disorder 62 14.275
7
P PTT006 Pituitary Adenoma 55 14.036
8
ADN018 Adenoma 58 13.862
9
P PNC025 Panic Disorder 52 13.862
10
PST028 Post-Traumatic Stress Disorder 59 13.505
11
ANX010 Anxiety 70 13.066
12
P HYP083 Hypopituitarism 52 13.024
13
ANR007 Anorexia Nervosa 59 13.001
14
P PHC003 Pheochromocytoma 70 12.999
15
c PRC016 Pre-Eclampsia 64 12.981
16
P BPL003 Bipolar Disorder 56 12.486
17
PST021 Postpartum Depression 50 12.469
18
WST001 West Syndrome 64 12.058
19
FBR047 Fibromyalgia 58 11.961
20
ACR007 Acromegaly 70 11.942
21
ADR008 Adrenal Adenoma 55 11.778
22
CHR066 Chronic Fatigue Syndrome 60 11.639
23
IRR002 Irritable Bowel Syndrome 65 11.066
24
P EPL164 Epilepsy 70 11.051
25
MNT002 Mental Depression 56 10.987
26
ALC007 Alcohol Dependence 65 10.650
27
ADR005 Adrenal Carcinoma 61 10.522
28
P AST005 Asthma 76 10.396
29
END040 Endogenous Depression 54 10.216
30
PTT009 Pituitary Gland Disease 53 10.097
31
AMN001 Amenorrhea 53 10.077
32
HYP780 Hypoadrenocorticism, Familial 61 10.070
33
ETN001 Eating Disorder 59 9.933
34
HYP005 Hypokalemia 55 9.925
35
PTT003 Pituitary-Dependent Cushing's Disease 39 9.776
36
P DBT005 Diabetes Insipidus 54 9.621
37
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 9.606
38
MLN003 Melancholia 41 9.517
39
P PRS038 Personality Disorder 65 9.441
40
HYP085 Hypothalamic Disease 38 9.301
41
BCT002 Bacterial Vaginosis 53 9.240
42
P SCH015 Schizophrenia 74 9.153
43
P RTT002 Rett Syndrome 79 9.119
44
P INT099 Intrahepatic Cholestasis of Pregnancy 61 9.029
45
c HYP595 Hypertension, Essential 84 8.818
46
SHH001 Sheehan Syndrome 44 8.683
47
ANV001 Anovulation 46 8.642
48
P WLF004 Wolfram Syndrome 61 8.562
49
OBS002 Obsessive-Compulsive Disorder 68 8.544
50
LPT014 Leptin Deficiency or Dysfunction 77 8.544
51
BRD004 Borderline Personality Disorder 53 8.544
52
GNG008 Ganglioneuroblastoma 46 8.544
53
P OLV001 Olivopontocerebellar Atrophy 51 8.524
54
PTT008 Pituitary Carcinoma 47 8.480
55
ESN002 Eosinophilia-Myalgia Syndrome 40 8.480
56
NLS001 Nelson Syndrome 43 8.480
57
DRG003 Drug Dependence 46 8.426
58
P DBT009 Diabetes Mellitus 67 8.392
59
ACT084 Acute Stress Disorder 53 8.355
60
ILS001 Ileus 49 8.240
61
P SZR006 Seizure Disorder 69 8.002
62
P ACT010 Acth-Secreting Pituitary Adenoma 60 7.822
63
P SLP005 Sleep Disorder 62 7.478
64
WTH001 Withdrawal Disorder 47 7.389
65
ATY001 Atypical Depressive Disorder 45 7.365
66
P ALC033 Alcohol Use Disorder 67 7.192
67
ACT238 Acth Deficiency, Isolated 52 7.147
68
PNG002 Pain Agnosia 51 7.094
69
FML063 Familial Glucocorticoid Deficiency 58 7.087
70
FST010 Fasting Hypoglycemia 33 6.954
71
P SBS003 Substance Abuse 54 6.864
72
ADJ001 Adjustment Disorder 46 6.706
73
SMT001 Somatization Disorder 50 6.706
74
MRP001 Morphine Dependence 41 6.687
75
DYS009 Dysthymic Disorder 51 6.687
76
AGR002 Agoraphobia 45 6.598
77
c EPL073 Epilepsy, Nocturnal Frontal Lobe, 1 47 6.598
78
DSS008 Disease of Mental Health 74 6.572
79
FNC007 Functioning Pituitary Adenoma 42 6.572
80
SMT006 Somatoform Disorder 50 6.570
81
ADR010 Adrenal Cortical Hypofunction 31 6.535
82
BNS003 Binswanger's Disease 41 6.353
83
GNG005 Gangliocytoma 54 6.295
84
OPT003 Opiate Dependence 49 6.269
85
c WLF013 Wolfram Syndrome 1 60 6.149
86
P ACT092 Acth-Independent Macronodular Adrenal Hyperplasia 56 6.149
87
c MGR028 Migraine with or Without Aura 1 64 6.090
88
ECT093 Ectopic Cushing Syndrome 45 6.090
89
SBS004 Substance Dependence 46 6.041
90
CNV002 Conversion Disorder 47 5.934
91
ADL002 Adult Syndrome 69 5.827
92
c PNS012 Paine Syndrome 60 5.827
93
MXD001 Mixed Cerebral Palsy 20 5.827
94
SPC003 Specific Developmental Disorder 31 5.827
95
END036 Endocrine Organ Benign Neoplasm 24 5.827
96
PHB003 Phobia, Specific 44 5.827
97
c PRK071 Parkinson Disease 14, Autosomal Recessive 42 5.827
98
SCL003 Social Phobia 48 5.827
99
HMT008 Hematuria, Benign Familial 53 5.827
100
TBC004 Tobacco Addiction 63 5.827
101
PTT010 Pituitary Infarct 32 5.827
102
PHB001 Phobic Disorder 45 5.827
103
PRS030 Persistent Fetal Circulation Syndrome 50 5.827
104
SXL001 Sexual Sadism 31 5.827
105
P AGN002 Agnosia 53 5.827
106
ADR009 Adrenal Cortex Disease 36 5.827
107
HYP070 Hyperpituitarism 36 5.827
108
INP001 Inappropriate Adh Syndrome 48 5.827
109
ADR012 Adrenal Gland Disease 44 5.827
110
MXD020 Mixed Cell Adenoma 30 5.827
111
PTT037 Pituitary Tumors 44 3.837
112
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 3.121
113
ADR040 Adrenal Gland Pheochromocytoma 45 2.765
114
PPL052 Papillomatosis, Confluent and Reticulated 34 2.726
115
c MJR024 Major Affective Disorder 9 40 2.388
116
c MJR022 Major Affective Disorder 8 37 2.388
117
NRN004 Neuroendocrine Tumor 55 2.216
118
SKN016 Skin Disease 62 2.090
119
ALL029 Allergic Disease 61 2.088
120
P ALP008 Alopecia 53 2.076
121
P ESP024 Esophagitis 60 1.982
122
P END044 Endometriosis 62 1.965
123
HYP266 Hypoxia 56 1.960
124
PST011 Pustulosis of Palm and Sole 52 1.887
125
P PSR002 Psoriasis 63 1.887
126
THY029 Thyroid Carcinoma 54 1.830
127
THY111 Thyroid Carcinoma, Familial Medullary 67 1.789
128
END041 Endometrial Adenocarcinoma 63 1.784
129
CHR074 Choriocarcinoma 46 1.782
130
THY125 Thyroid Gland Medullary Carcinoma 48 1.782
131
P DRM053 Dermatitis, Atopic 65 1.765
132
HYP080 Hypogonadism 49 1.653
133
P HYP086 Hypothyroidism 69 1.646
134
c SCN052 Secondary Adrenal Insufficiency 35 1.646
135
TXC005 Toxic Shock Syndrome 62 1.635
136
CYT002 Cytokine Deficiency 43 1.603
137
P SML001 Small Cell Carcinoma 52 1.571
138
P RHM011 Rheumatoid Arthritis 81 1.512
139
c PRM093 Premature Ovarian Failure 7 47 1.507
140
SVR004 Severe Combined Immunodeficiency 71 1.468
141
END057 Endometrial Cancer 71 1.440
142
CRV035 Cervical Cancer 72 1.429
143
PRT037 Pertussis 49 1.429
144
HYP066 Hyperglycemia 60 1.404
145
BHR001 Behr Syndrome 50 1.401
146
DYS011 Dyskinesia of Esophagus 40 1.401
147
P ALP061 Alopecia, Androgenetic, 1 49 1.394
148
AND014 Androgenic Alopecia 46 1.394
149
CLT003 Colitis 63 1.367
150
CHL014 Cholera 62 1.345
151
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.345
152
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 1.345
153
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.345
154
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.345
155
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 1.345
156
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.345
157
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.345
158
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 1.345
159
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 1.345
160
P MSC003 Muscular Atrophy 52 1.345
161
DRM006 Dermatitis 62 1.331
162
CHR005 Chorioamnionitis 50 1.324
163
BRN053 Bronchial Adenomas/carcinoids Childhood 22 1.323
164
CRC014 Carcinoid Tumors, Intestinal 46 1.252
165
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 1.227
166
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 1.227
167
ATM095 Autoimmune Disease 61 1.227
168
P PLY011 Polycystic Ovary Syndrome 57 1.227
169
P SPR120 Supranuclear Palsy, Progressive, 1 69 1.203
170
CRC006 Carcinoid Syndrome 55 1.201
171
c ATS007 Autism Spectrum Disorder 72 1.173
172
P HNT016 Huntington Disease 73 1.159
173
c DWL002 Dowling-Degos Disease 1 58 1.145
174
P MST009 Mastocytosis 64 1.127
175
P ECL001 Eclampsia 52 1.120
176
ULC004 Ulcerative Colitis 74 1.104
177
GRW007 Growth Hormone Deficiency 47 1.093
178
SPN392 Spondylosis, Cervical 30 1.050
179
SPN020 Spondylosis 46 1.050
180
CCN001 Cocaine Dependence 48 1.037
181
P BRS047 Breast Cancer 97 1.035
182
SXL003 Sexual Disorder 49 1.025
183
P INF032 Infertility 60 1.025
184
ACT245 Acth-Dependent Cushing Syndrome 23 1.025
185
CHL068 Cholestasis 61 1.018
186
P ATS364 Autism 72 1.012
187
P MYP004 Myopathy 67 1.012
188
P ALP009 Alopecia Areata 59 1.012
189
PSY004 Psychotic Disorder 66 1.010
190
ISL001 Islet Cell Tumor 55 0.986
191
OPD006 Opioid Addiction 48 0.973
192
CCN002 Cocaine Abuse 49 0.973
193
CRB004 Cerebral Artery Occlusion 46 0.972
194
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.958
195
P SPP010 Suppressor of Tumorigenicity 3 51 0.944
196
PRT251 Proteinuria, Chronic Benign 58 0.944
197
P OST002 Osteoporosis 77 0.944
198
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.944
199
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.944
200
AVD001 Avoidant Personality Disorder 49 0.944
201
LVR012 Liver Cirrhosis 62 0.944
202
c BPL002 Bipolar I Disorder 47 0.944
203
P ALZ034 Alzheimer Disease 87 0.929
204
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.929
205
PCD001 Pica Disease 38 0.929
206
P MJR007 Major Affective Disorder 1 42 0.913
207
NRN001 Neuroendocrine Carcinoma 47 0.913
208
P CLR023 Colorectal Cancer 100 0.904
209
ADN027 Adenomyosis 59 0.896
210
ZLL002 Zollinger-Ellison Syndrome 55 0.896
211
DNT005 Dentatorubral-Pallidoluysian Atrophy 59 0.896
212
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 0.896
213
P DRR001 Diarrhea 55 0.896
214
P ACN011 Acne 55 0.891
215
P OVR042 Ovarian Cancer 88 0.879
216
KRT071 Keratosis, Seborrheic 56 0.879
217
KRT009 Keratosis 52 0.879
218
PRN039 Paraneoplastic Syndromes 37 0.879
219
P FBR031 Febrile Seizures 52 0.879
220
INV005 Inverted Follicular Keratosis 32 0.879
221
RCK004 Rickets 65 0.860
222
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.860
223
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.860
224
ACQ007 Acquired Immunodeficiency Syndrome 58 0.860
225
GST010 Gestational Trophoblastic Neoplasm 52 0.860
226
GST030 Gastrinoma 45 0.860
227
THY092 Thymic Neuroendocrine Carcinoma 14 0.860
228
P ART022 Arthritis 70 0.845
229
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.841
230
PRT036 Peritonitis 65 0.841
231
PLC008 Placenta Disease 49 0.824
232
OCL069 Ocular Motor Apraxia 57 0.820
233
c INF002 Inflammatory Diarrhea 30 0.820
234
RBS001 Rabies 58 0.820
235
STT001 Status Epilepticus 58 0.820
236
DMN012 Dementia - Subcortical 17 0.820
237
CRN036 Craniopharyngioma 63 0.797
238
SCH003 Schizophreniform Disorder 54 0.790
239
48X005 48,xyyy 39 0.781
240
c NRB010 Neuroblastoma 1 60 0.774
241
PLM010 Pulmonary Edema 54 0.771
242
PRS064 Persistent Vegetative State 33 0.771
243
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.763
244
INS024 Insulin-Like Growth Factor I 77 0.743
245
P LKM002 Leukemia 66 0.743
246
LBS001 Lubs X-Linked Mental Retardation Syndrome 49 0.743
247
P ASP006 Aspergillosis 71 0.743
248
P CND004 Candidiasis 57 0.743
249
CHR034 Chromophobe Adenoma 35 0.743
250
P NRB001 Neuroblastoma 66 0.720
251
INT395 Intracranial Meningioma 48 0.709
252
ASP004 Asphyxia Neonatorum 50 0.709
253
MNN043 Meningioma, Familial 79 0.709
254
SCR001 Secretory Meningioma 40 0.709
255
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.709
256
c PRM340 Primary Adrenal Insufficiency 37 0.704
257
P LKM062 Leukemia, Acute Lymphoblastic 69 0.695
258
ING001 Inguinal Hernia 59 0.664
259
HYP017 Hypophosphatemia 49 0.664
260
P ADL010 Adult Respiratory Distress Syndrome 71 0.664
261
c ATM075 Autoimmune Encephalitis 39 0.664
262
P THY032 Thyroiditis 56 0.661
263
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.638
264
PTT057 Pituitary Adenoma 4, Acth-Secreting 48 0.638
265
PPL001 Papillary Adenoma 44 0.638
266
NRT001 Neurotic Disorder 56 0.638
267
HYP705 Hyperadrenalism 24 0.638
268
HYP060 Hyperinsulinism 53 0.626
269
P CYS018 Cystitis 59 0.626
270
P PRS040 Prostate Cancer 95 0.625
271
PSR001 Psoriatic Arthritis 61 0.607
272
47X002 47,xyy 48 0.597
273
P URT039 Urticaria 57 0.578
274
P INT143 Interstitial Cystitis 59 0.568
275
GLC106 Glucocorticoid Resistance, Generalized 48 0.558
276
HSH003 Hashimoto Thyroiditis 60 0.558
277
VSC002 Vascular Dementia 59 0.558
278
P TRT010 Teratoma 50 0.557
279
LPD008 Lipid Metabolism Disorder 61 0.547
280
HYP020 Hyperprolactinemia 63 0.537
281
P UVT001 Uveitis 57 0.537
282
CNS004 Constipation 56 0.526
283
ADN011 Adenoid Cystic Carcinoma 68 0.517
284
P PNC035 Pancreatic Cancer 86 0.517
285
SZR001 Sezary's Disease 60 0.517
286
HYP043 Hyperandrogenism 47 0.515
287
BRN071 Brain Injury 50 0.515
288
TRM010 Traumatic Brain Injury 50 0.515
289
P MYT002 Myotonic Dystrophy 51 0.515
290
LPD012 Lipoid Congenital Adrenal Hyperplasia 68 0.503
291
ALL014 Allergic Encephalomyelitis 34 0.503
292
P RTN024 Retinoblastoma 72 0.492
293
P LYM033 Lymphoproliferative Syndrome 59 0.480
294
c LKM061 Leukemia, Acute Myeloid 83 0.480
295
P ENC018 Encephalopathy 62 0.480
296
P MYL006 Myeloid Leukemia 60 0.480
297
P HYP263 Hypersomnia 40 0.480
298
P HYP076 Hyperthyroidism 53 0.480
299
PTT046 Pituitary Hormone Deficiency, Combined, 2 62 0.468
300
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.468
301
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.468
302
P SLP006 Sleep Apnea 69 0.455
303
GLC003 Glucose Intolerance 53 0.442
304
ADR041 Adrenal Cortical Adenoma 48 0.442
305
HND015 Hand Skill, Relative 29 0.442
306
BRN004 Brain Edema 54 0.442
307
P MLT074 Multiple Endocrine Neoplasia 58 0.442
308
P CHR345 Chronic Pain 50 0.442
309
PPT005 Peptic Ulcer Disease 58 0.442
310
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 0.429
311
ENT011 Enterocolitis 55 0.429
312
c CHR708 Chronic Urticaria 42 0.429
313
PRM020 Premenstrual Tension 39 0.429
314
c ACT075 Acute Myocardial Infarction 55 0.429
315
P BLD134 Bladder Cancer 79 0.416
316
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.416
317
AGN016 Aging 54 0.416
318
ATH013 Atherosclerosis Susceptibility 63 0.416
319
PLC001 Placenta Accreta 44 0.416
320
P KDN017 Kidney Cancer 60 0.416
321
P ACT105 Acute Mountain Sickness 52 0.416
322
GST092 Gastroesophageal Reflux 60 0.402
323
ADR016 Adrenal Cortical Carcinoma 61 0.402
324
c TYP008 Type 1 Diabetes Mellitus 77 0.402
325
c SVR005 Severe Pre-Eclampsia 50 0.402
326
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.402
327
c MCR115 Microvascular Complications of Diabetes 5 65 0.387
328
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.387
329
CNG034 Congestive Heart Failure 69 0.387
330
P GST044 Gastritis 55 0.387
331
P INF037 Inflammatory Bowel Disease 53 0.372
332
CNT047 Contact Dermatitis 57 0.372
333
SYN007 Synovitis 54 0.372
334
PLC002 Plica Syndrome 35 0.372
335
END086 End Stage Renal Disease 54 0.372
336
P HYP730 Hypogonadotropic Hypogonadism 54 0.356
337
P MLT020 Multiple Sclerosis 79 0.356
338
MTB004 Metabolic Acidosis 48 0.356
339
c HYP836 Hypercholesterolemia, Familial, 1 73 0.356
340
P HYP750 Hypertriglyceridemia, Familial 62 0.356
341
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.356
342
P TMP003 Temporal Arteritis 68 0.356
343
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 55 0.339
344
PTT004 Pituitary Apoplexy 47 0.339
345
P HPT023 Hepatocellular Carcinoma 95 0.339
346
c BSL007 Basal Cell Carcinoma 68 0.339
347
P OBS001 Obstructive Jaundice 49 0.339
348
P LVR013 Liver Disease 68 0.339
349
DWR001 Dwarfism 45 0.339
350
TRY001 Trypanosomiasis 50 0.322
351
ECT026 Ectopic Pregnancy 47 0.322
352
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.322
353
EMP001 Empty Sella Syndrome 42 0.322
354
P CRN300 Coronary Heart Disease 1 73 0.322
355
BCK006 Back Pain 43 0.322
356
P HRP006 Herpes Simplex 65 0.322
357
P NRC002 Narcolepsy 55 0.322
358
HDN002 Head Injury 44 0.322
359
OST012 Osteoarthritis 77 0.322
360
ORG003 Organic Mood Syndrome 13 0.322
361
c TYP009 Type 2 Diabetes Mellitus 92 0.304
362
CLB010 Coloboma of Macula 53 0.304
363
HMN044 Human Immunodeficiency Virus Type 1 76 0.304
364
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.304
365
FCL012 Facial Paralysis 49 0.304
366
P DDN001 Duodenal Ulcer 53 0.304
367
MNC001 Monocular Esotropia 30 0.304
368
P HYP077 Hypertrichosis 48 0.304
369
ADR004 Adrenal Cortical Adenocarcinoma 38 0.304
370
CRB090 Cerebral Hypoxia 42 0.304
371
CRV002 Cervix Uteri Carcinoma in Situ 48 0.304
372
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.304
373
MYT011 Myotonia 38 0.304
374
CRV045 Cervical Intraepithelial Neoplasia 38 0.304
375
SBC016 Subacute Delirium 42 0.304
376
HYP034 Hypertensive Encephalopathy 43 0.304
377
EST005 Esotropia 42 0.304
378
P HYP098 Hypereosinophilic Syndrome 66 0.304
379
c HYP795 Hypothyroidism, Congenital, Nongoitrous, 4 47 0.284
380
DWN001 Down Syndrome 70 0.284
381
P GST053 Gastric Cancer 82 0.284
382
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 46 0.284
383
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 0.284
384
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.284
385
MDD018 Middle East Respiratory Syndrome 44 0.284
386
EXT054 Extra-Adrenal Pheochromocytoma 31 0.284
387
STT041 Stuttering 52 0.284
388
BLM002 Bulimia Nervosa 57 0.284
389
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.284
390
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.284
391
HPT004 Hepatic Coma 43 0.284
392
HPT019 Hepatic Encephalopathy 59 0.284
393
P HYD006 Hydrocephalus 63 0.284
394
CHL123 Chlamydia 58 0.284
395
P NTR004 Neutropenia 62 0.284
396
P GRV001 Graves' Disease 54 0.284
397
GST023 Gastric Ulcer 52 0.284
398
INS001 Insulinoma 59 0.284
399
P MYC033 Myoclonus 46 0.284
400
P LCH002 Lichen Planus 55 0.284
401
P HDC001 Headache 56 0.284
402
SPN050 Spinocerebellar Degeneration 39 0.284
403
ORL011 Oral Cancer 60 0.284
404
RTC012 Reticuloendotheliosis, X-Linked 35 0.263
405
c PNC068 Panic Disorder 3 12 0.263
406
c PRM108 Primary Progressive Multiple Sclerosis 51 0.263
407
P MDL005 Medulloblastoma 75 0.263
408
c CNG006 Congenital Hypothyroidism 63 0.263
409
CRB028 Cerebellar Medulloblastoma 33 0.263
410
P MYC007 Myocardial Infarction 69 0.263
411
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.263
412
PRV004 Periventricular Leukomalacia 52 0.263
413
P BNG030 Benign Ependymoma 51 0.263
414
ART002 Arts Syndrome 66 0.263
415
SPP011 Suppression of Tumorigenicity 12 61 0.263
416
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.263
417
P TRM003 Tremor 50 0.263
418
CLL010 Cellular Ependymoma 58 0.263
419
BRN056 Bronchopulmonary Dysplasia 57 0.263
420
c ACT150 Acute Adrenal Insufficiency 48 0.263
421
CRD137 Cardiogenic Shock 56 0.263
422
NNL006 Non-Alcoholic Steatohepatitis 54 0.240
423
ALX002 Alexithymia 37 0.240
424
c SCL052 Scleroderma, Familial Progressive 60 0.240
425
P INT068 Intestinal Disease 53 0.240
426
OVR063 Overnutrition 42 0.240
427
HMN048 Human Papillomavirus Infectious Disease 46 0.240
428
GST033 Gestational Diabetes 61 0.240
429
PLC005 Placental Insufficiency 56 0.240
430
P SKN015 Skin Carcinoma 71 0.240
431
CNG184 Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects 56 0.240
432
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.240
433
FSC004 Fasciitis 49 0.240
434
c CNT101 Central Congenital Hypothyroidism 37 0.240
435
LYM043 Lymphocytic Hypophysitis 31 0.240
436
KWS002 Kawasaki Disease 65 0.215
437
P RST001 Restless Legs Syndrome 52 0.215
438
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.215
439
PRT013 Portal Hypertension 59 0.215
440
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.215
441
APH002 Aphasia 55 0.215
442
ORL015 Oral Squamous Cell Carcinoma 43 0.215
443
P CRD119 Cardiac Arrest 68 0.215
444
c PRG020 Paragangliomas 3 39 0.215
445
P PRD006 Prader-Willi Syndrome 60 0.215
446
ISC004 Ischemia 61 0.215
447
P ADN016 Adenocarcinoma 63 0.215
448
P GRW001 Growth Hormone Secreting Pituitary Adenoma 47 0.215
449
c ACT042 Acute Pyelonephritis 45 0.215
450
URM002 Uremia 47 0.215
451
IMP005 Impotence 52 0.215
452
IRN002 Iron Metabolism Disease 56 0.215
453
SHG001 Shigellosis 61 0.215
454
P PYL005 Pyelonephritis 56 0.215
455
P PLM036 Pulmonary Fibrosis 65 0.215
456
WLL004 Wallerian Degeneration 38 0.215
457
P KDN018 Kidney Disease 72 0.215
458
P PNM007 Pneumonia 64 0.215
459
MCP006 Mucoepidermoid Carcinoma 48 0.215
460
DRM011 Dermatophytosis 52 0.215
461
c BCT013 Bacterial Pneumonia 47 0.215
462
P PRC019 Precocious Puberty 49 0.215
463
HYP835 Hypothalamic Obesity 38 0.215
464
c SPR119 Spermatogenic Failure, X-Linked, 1 36 0.186
465
c GLL024 Gallbladder Disease 1 53 0.186
466
P GRF003 Graft-Versus-Host Disease 71 0.186
467
SCH011 Schizotypal Personality Disorder 36 0.186
468
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.186
469
MCS002 Mucositis 55 0.186
470
CHY002 Chylomicron Retention Disease 64 0.186
471
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.186
472
P EXN002 Exanthem 58 0.186
473
PRT010 Parathyroid Carcinoma 68 0.186
474
LNG108 Langerhans Cell Histiocytosis 57 0.186
475
c HPT073 Hepatitis C Virus 71 0.186
476
MCC012 Mccune-Albright Syndrome 69 0.186
477
P PTS002 Ptosis 52 0.186
478
GYN001 Gynecomastia 48 0.186
479
CND002 Conduct Disorder 50 0.186
480
CMP010 Complex Regional Pain Syndrome 59 0.186
481
CRB027 Cerebellar Disease 47 0.186
482
NPH009 Nephrolithiasis 54 0.186
483
P DYS154 Dystonia 64 0.186
484
P MCR010 Microcephaly 59 0.186
485
c HPT001 Hepatitis C 61 0.186
486
HYP016 Hypochondriasis 47 0.186
487
P HYP050 Hyperinsulinemic Hypoglycemia 56 0.186
488
MYS004 Myiasis 38 0.186
489
INF021 Infant Gynecomastia 30 0.186
490
OLF005 Olfactory Neuroblastoma 46 0.186
491
ALL010 Allergic Contact Dermatitis 56 0.186
492
P BRS044 Breast Adenocarcinoma 58 0.186
493
HST010 Histiocytosis 49 0.186
494
TNC002 Tinea Capitis 42 0.186
495
P PSD015 Pseudohypoparathyroidism 54 0.186
496
DMY004 Demyelinating Disease 50 0.186
497
CRB081 Cerebellar Ataxia, Cayman Type 39 0.186
498
OST159 Osteogenic Sarcoma 66 0.186
499
P NSP012 Nasopharyngeal Carcinoma 60 0.186
500
GST045 Gastroenteritis 58 0.186
501
ANX004 Anoxia 40 0.186
502
LNG099 Lung Disease 62 0.186
503
VRL011 Viral Infectious Disease 60 0.186
504
PLM013 Pulmonary Immaturity 30 0.186
505
MLT001 Multiple Chemical Sensitivity 38 0.186
506
P MSC005 Muscular Dystrophy 66 0.186
507
HYP231 Hypothalamic Hamartomas 33 0.186
508
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.186
509
THY108 Thymic Neuroendocrine Tumor 32 0.186
510
P SRC025 Sarcoidosis 1 70 0.152
511
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.152
512
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.152
513
MYL069 Myeloma, Multiple 77 0.152
514
c GRV008 Graves Disease 1 54 0.152
515
HMC014 Homocysteinemia 52 0.152
516
P PLM037 Pulmonary Hypertension 69 0.152
517
HRT040 Hirata Disease 38 0.152
518
BCT022 Bacterial Infectious Disease 56 0.152
519
BNR002 Bone Resorption Disease 47 0.152
520
c SPN225 Spondyloarthropathy 1 70 0.152
521
IMM167 Immune Deficiency Disease 77 0.152
522
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.152
523
ISL003 Isolated Growth Hormone Deficiency 57 0.152
524
BCT021 Bacterial Sepsis 43 0.152
525
P CRN038 Carney Complex Variant 63 0.152
526
LNT004 Lentigines 45 0.152
527
P HYP726 Hypercalcemia, Infantile, 1 58 0.152
528
MST024 Mastocytosis, Cutaneous 66 0.152
529
MTN003 Motion Sickness 50 0.152
530
c PLM164 Pulmonary Hypertension, Primary, 1 80 0.152
531
c SML038 Small Cell Cancer of the Lung 69 0.152
532
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.152
533
ACT088 Acute Insulin Response 39 0.152
534
ACD008 Acid-Labile Subunit Deficiency 52 0.152
535
c SCH079 Schizophrenia 1 44 0.152
536
IGR001 Ige Responsiveness, Atopic 59 0.152
537
NRT004 Neuritis 53 0.152
538
P PRG013 Paraganglioma 57 0.152
539
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.152
540
DFC004 Deficiency Anemia 74 0.152
541
MST005 Mastitis 52 0.152
542
c FML021 Familial Hypercholesterolemia 71 0.152
543
c ACT027 Acute Pancreatitis 60 0.152
544
LYM027 Lymphopenia 56 0.152
545
SPN051 Spondylitis 51 0.152
546
MYL031 Myeloproliferative Neoplasm 66 0.152
547
SCK001 Sick Building Syndrome 33 0.152
548
P MLN008 Melanoma 75 0.152
549
SCH014 Schistosomiasis 56 0.152
550
GNR004 Generalized Anxiety Disorder 55 0.152
551
P OPT009 Optic Neuritis 57 0.152
552
INF009 Inflammatory Spondylopathy 30 0.152
553
CHL004 Cholelithiasis 48 0.152
554
ATN004 Autonomic Neuropathy 42 0.152
555
PLS011 Plasmacytoma 56 0.152
556
FCL014 Focal Epilepsy 53 0.152
557
P ART021 Arteriosclerosis 53 0.152
558
PPL002 Papillary Carcinoma 46 0.152
559
SDD001 Sudden Infant Death Syndrome 60 0.152
560
HRT012 Heart Valve Disease 53 0.152
561
P CLS010 Cluster Headache 42 0.152
562
SPC005 Speech Disorder 46 0.152
563
PTH003 Pathologic Nystagmus 52 0.152
564
PYD002 Pyoderma 49 0.152
565
PLX002 Plexiform Neurofibroma 44 0.152
566
c JVN010 Juvenile Rheumatoid Arthritis 66 0.152
567
SPN186 Spinal Cord Injury 61 0.152
568
P CRB059 Cerebellar Degeneration 36 0.152
569
HPT022 Hepatoblastoma 54 0.152
570
PYD001 Pyoderma Gangrenosum 53 0.152
571
FTT001 Fatty Liver Disease 61 0.152
572
NRF007 Neurofibroma 64 0.152
573
PRN019 Perinatal Necrotizing Enterocolitis 60 0.152
574
P NRF002 Neurofibromatosis 60 0.152
575
CRP002 Croup 42 0.152
576
LRN003 Learning Disability 49 0.152
577
THY128 Thyroid Tumor 33 0.152
578
PRT058 Pure Autonomic Failure 58 0.152
579
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.152
580
P ACT244 Acth-Independent Cushing Syndrome 37 0.152
581
ART140 Arteries, Anomalies of 52 0.107
582
c FBR073 Febrile Seizures, Familial, 1 40 0.107
583
GLC096 Galactorrhea 40 0.107
584
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.107
585
PRS129 Prostatic Hyperplasia, Benign 48 0.107
586
MYC080 Myoclonic Epilepsy of Unverricht and Lundborg 52 0.107
587
c HYP374 Hypothyroidism, Congenital, Nongoitrous, 1 51 0.107
588
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.107
589
c ATM024 Autoimmune Pancreatitis 52 0.107
590
LPP008 Lipoprotein Quantitative Trait Locus 65 0.107
591
HLX001 Helix Syndrome 47 0.107
592
ATS010 Autosomal Recessive Disease 42 0.107
593
DFF005 Diffuse Large B-Cell Lymphoma 55 0.107
594
LNN001 Lennox-Gastaut Syndrome 61 0.107
595
MLD018 Mild Cognitive Impairment 48 0.107
596
P SNS001 Sensorineural Hearing Loss 59 0.107
597
FBR009 Fibrous Dysplasia 48 0.107
598
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.107
599
SLP001 Sleeping Sickness 56 0.107
600
PRM013 Premature Menopause 57 0.107
601
c PSD108 Pseudohypoparathyroidism, Type Ia 64 0.107
602
c ATR087 Atrial Standstill 1 74 0.107
603
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.107
604
BDY001 Body Dysmorphic Disorder 40 0.107
605
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 59 0.107
606
PYG003 Pyogenic Sterile Arthritis, Pyoderma Gangrenosum, and Acne 55 0.107
607
PRT082 Preterm Premature Rupture of the Membranes 56 0.107
608
PTC002 Potocki-Lupski Syndrome 51 0.107
609
OBS081 Obesity, Early-Onset, with Adrenal Insufficiency and Red Hair 37 0.107
610
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.107
611
ALL003 Allergic Rhinitis 66 0.107
612
APR006 Apert Syndrome 69 0.107
613
MTP034 Metaphyseal Chondrodysplasia, Jansen Type 50 0.107
614
PBL005 Piebald Trait 59 0.107
615
DBT087 Diabetes Insipidus, Neurohypophyseal 58 0.107
616
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.107
617
EWN003 Ewing Sarcoma 70 0.107
618
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.107
619
CHL065 Cholangiocarcinoma 58 0.107
620
SRC014 Sarcoma 64 0.107
621
GLC042 Glucocorticoid Deficiency 1 49 0.107
622
c MLT160 Multiple Endocrine Neoplasia, Type Iia 67 0.107
623
STF001 Stiff-Person Syndrome 57 0.107
624
WLL001 Williams-Beuren Syndrome 60 0.107
625
HMP005 Hemiplegia 53 0.107
626
PHY002 Physical Disorder 41 0.107
627
c ACT073 Acute Leukemia 59 0.107
628
P TBR001 Tuberous Sclerosis 69 0.107
629
GLB002 Glioblastoma 67 0.107
630
ETH004 Euthyroid Sick Syndrome 38 0.107
631
HYP029 Hyperthyroxinemia 32 0.107
632
PRS021 Prostatic Adenoma 43 0.107
633
PLM001 Pulmonary Tuberculosis 69 0.107
634
CRB039 Cerebrovascular Disease 65 0.107
635
INT079 Intrahepatic Cholangiocarcinoma 51 0.107
636
NTR005 Nutritional Deficiency Disease 60 0.107
637
AMN003 Amnestic Disorder 54 0.107
638
PRS045 Prostatic Hypertrophy 52 0.107
639
CHL067 Cholecystitis 59 0.107
640
CRB037 Cerebral Palsy 67 0.107
641
P DMN002 Dementia 65 0.107
642
TYP007 Typhoid Fever 63 0.107
643
SQM006 Squamous Cell Carcinoma 59 0.107
644
P CRD246 Cardiovascular System Disease 55 0.107
645
CNT019 Central Neurocytoma 46 0.107
646
BNG006 Benign Familial Neonatal Epilepsy 54 0.107
647
DSS009 Disseminated Intravascular Coagulation 56 0.107
648
GTR002 Goiter 52 0.107
649
CHG001 Chagas Disease 65 0.107
650
P MNN007 Meningocele 39 0.107
651
ERL001 Early Myoclonic Encephalopathy 63 0.107
652
LNG039 Lung Squamous Cell Carcinoma 57 0.107
653
P GLY013 Glycogen Storage Disease 59 0.107
654
P RHN004 Rhinitis 57 0.107
655
VGN023 Vaginitis 56 0.107
656
P TMP001 Temporal Lobe Epilepsy 49 0.107
657
DRV001 Dravet Syndrome 70 0.107
658
ADR007 Adrenoleukodystrophy 74 0.107
659
NRM005 Neuromuscular Disease 63 0.107
660
SPN035 Spindle Cell Sarcoma 51 0.107
661
PRP030 Purpura 54 0.107
662
SPH001 Sapho Syndrome 47 0.107
663
P HYP120 Hypoaldosteronism 33 0.107
664
IDP031 Idiopathic Hypersomnia 39 0.107
665
MST020 Mast Cell Activation Syndrome 27 0.107
666
ODN006 Odontoma 29 0.107
667
SFT003 Soft Tissue Sarcoma 57 0.107
668
c SBC007 Subacute Thyroiditis 43 0.107
669
SYN036 Syncope 44 0.107
670
P HYP265 Hypotonia 42 0.107
671
INT075 Intracranial Hypertension 52 0.107
672
GNG004 Ganglioglioma 53 0.107
673
SPL018 Splenomegaly 47 0.107
674
GNT046 Genetic Epilepsy with Febrile Seizures Plus 29 0.107
675
c ALM001 Al Amyloidosis 54 0.107
676
ADR022 Adrenomyeloneuropathy 39 0.107
677
BRK012 Broken Heart Syndrome 42 0.107
678
P RTN016 Retinal Degeneration 52 0.107
679
P AMY004 Amyloidosis 69 0.107
680
P BCL017 B-Cell Lymphoma 57 0.107
681
DLS001 Delusional Disorder 44 0.107
682
GST050 Gastrointestinal System Disease 55 0.107
683
P HMR005 Hemorrhoid 49 0.107
684
3BT001 3-Beta-Hydroxysteroid Dehydrogenase Deficiency 40 0.107
685
INT059 Internal Hemorrhoid 35 0.107
686
MYL080 Myalgic Encephalomyelitis/chronic Fatigue Syndrome 32 0.107
687
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.107
688
EMB007 Embryonal Sarcoma 40 0.107
689
MNN022 Meningoencephalocele 21 0.107
690
MCR004 Macroglobulinemia 48 0.107
691
PST092 Posttransplant Acute Limbic Encephalitis 29 0.107
692
NRN046 Neuronal Tumor 19 0.107
693
c HRD156 Hereditary Central Diabetes Insipidus 24 0.107
694
NRN044 Neuroendocrine Carcinoma of Pancreas 17 0.107
695
ARG004 Argyria 26 0.107
696
P PHC019 Pheochromocytoma-Paraganglioma 35 0.107
697
c CHR695 Chronic Primary Adrenal Insufficiency 15 0.107
698
ADN064 Adenohypophysitis 34 0.107
699
c MYC068 Myoclonic Epilepsy of Infancy 34 0.107
700
BRN137 Bronchial Neuroendocrine Tumor 29 0.107
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