Search results for tyr

1631 hits were found for tyr

# Family MCID Name MIFTS Score
1
c ALB009 Albinism, Oculocutaneous, Type Ia 54 55.079
2
c ALB010 Albinism, Oculocutaneous, Type Ib 52 40.767
3
P OCL062 Ocular Albinism with Congenital Sensorineural Deafness 24 39.270
4
P OCL002 Oculocutaneous Albinism 59 37.583
5
ALB002 Albinism 46 34.693
6
c SKN068 Skin/hair/eye Pigmentation, Variation in, 3 25 31.208
7
P OCL001 Ocular Albinism 47 25.935
8
ALB025 Albinism, Ocular, with Late-Onset Sensorineural Deafness 50 21.986
9
P STR020 Strabismus 56 21.641
10
HYP854 Hypopigmentation of the Skin 22 19.144
11
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 18.495
12
P MYP006 Myopia 55 17.994
13
P OPT006 Optic Nerve Disease 57 17.951
14
PTH003 Pathologic Nystagmus 52 16.918
15
P MLN008 Melanoma 75 14.922
16
MCR013 Microphthalmia 59 12.928
17
P SKN015 Skin Carcinoma 71 11.870
18
SKN019 Skin Melanoma 70 11.798
19
AML001 Amelanotic Melanoma 37 11.692
20
c BSL007 Basal Cell Carcinoma 67 11.262
21
P HRM001 Hermansky-Pudlak Syndrome 65 10.855
22
P WRD001 Waardenburg's Syndrome 60 10.702
23
CHD001 Chediak-Higashi Syndrome 66 10.612
24
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 10.532
25
VGT001 Vogt-Koyanagi-Harada Disease 55 10.491
26
ANG018 Angiomyolipoma 45 10.370
27
P EYD002 Eye Disease 57 10.167
28
ATS010 Autosomal Recessive Disease 42 10.010
29
P MLN069 Melanoma, Uveal 59 9.692
30
SKN016 Skin Disease 63 9.424
31
P CNG024 Congenital Nystagmus 35 9.252
32
P ACT008 Actinic Keratosis 53 9.116
33
c ALB021 Albinism, Oculocutaneous, Type Ii 58 9.115
34
PGM003 Pigmentation Disease 45 8.929
35
NRL005 Neurilemmoma 60 8.738
36
SKN013 Skin Benign Neoplasm 49 8.694
37
P HMC002 Homocystinuria 52 8.638
38
CLR017 Clear Cell Sarcoma 44 8.553
39
NRF007 Neurofibroma 63 8.553
40
LYM007 Lymphangioleiomyomatosis 68 8.467
41
MLN079 Melanoma in Congenital Melanocytic Nevus 39 8.467
42
c MLN043 Melanoma, Cutaneous Malignant 8 38 8.252
43
c ALB019 Albinism, Oculocutaneous, Type Iv 48 7.538
44
MNM005 Minimal Pigment Oculocutaneous Albinism Type 1 7 7.334
45
c TYR012 Tyrosinemia, Type I 61 7.097
46
c ALB016 Albinism, Oculocutaneous, Type Vii 38 6.991
47
c DWL002 Dowling-Degos Disease 1 58 6.973
48
c ALB020 Albinism, Oculocutaneous, Type Iii 49 6.836
49
P MLN066 Melanoma, Cutaneous Malignant 1 65 6.800
50
P RTN008 Retinitis Pigmentosa 79 6.758
51
c WRD033 Waardenburg Syndrome, Type 2e 53 6.197
52
c ALB015 Albinism, Oculocutaneous, Type V 36 6.197
53
c WRD032 Waardenburg Syndrome, Type 2a 48 6.159
54
P GRS003 Griscelli Syndrome 54 6.159
55
MNK001 Menkes Disease 64 6.108
56
TTZ003 Tietz Albinism-Deafness Syndrome 59 6.108
57
NDL001 Nodular Malignant Melanoma 44 6.108
58
OCH001 Ochronosis 40 6.108
59
ACT011 Acute Contagious Conjunctivitis 41 6.073
60
ATM016 Autoimmune Disease of Skin and Connective Tissue 32 5.987
61
c NYS005 Nystagmus 4, Congenital, Autosomal Dominant 33 5.987
62
c WRD030 Waardenburg Syndrome, Type 1 54 5.987
63
KRT071 Keratosis, Seborrheic 56 5.987
64
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 50 5.987
65
MLN065 Melanocytic Nevus Syndrome, Congenital 62 5.987
66
GLL008 Gilles De La Tourette Syndrome 64 5.987
67
c ADV006 Advanced Sleep Phase Syndrome, Familial, 3 26 5.987
68
c ORF016 Orofacial Cleft 8 42 5.987
69
P NYS013 Nystagmus 6, Congenital, X-Linked 39 5.987
70
OCC006 Occipital Horn Syndrome 53 5.987
71
PBL005 Piebald Trait 60 5.987
72
c WRD031 Waardenburg Syndrome, Type 3 46 5.987
73
HLN001 Halo Nevi 27 5.987
74
c WRD020 Waardenburg Syndrome, Type 4a 49 5.987
75
c WRD019 Waardenburg Syndrome, Type 4b 46 5.987
76
c NYS016 Nystagmus 7, Congenital, Autosomal Dominant 27 5.987
77
c NYS003 Nystagmus 2, Congenital, Autosomal Dominant 31 5.987
78
MLN005 Melanoacanthoma 24 5.987
79
MLG005 Malignant Spindle Cell Melanoma 39 5.987
80
INT379 Integumentary System Disease 31 5.987
81
EPT001 Epithelioid Cell Melanoma 23 5.987
82
MNN010 Meningeal Melanoma 31 5.987
83
DFF013 Diffuse Meningeal Melanocytosis 23 5.987
84
CLR122 Ciliary Body Cancer 25 5.987
85
SRC007 Sarcomatoid Transitional Cell Carcinoma 26 5.987
86
ORB011 Orbit Rhabdomyosarcoma 34 5.987
87
c CHR059 Chronic Endophthalmitis 21 5.987
88
SPN025 Spinal Cord Melanoma 22 5.987
89
c ACT067 Acute Conjunctivitis 36 5.987
90
BLL005 Bullous Retinoschisis 20 5.987
91
MLG071 Malignant Leptomeningeal Tumor 26 5.987
92
MLG062 Malignant Ciliary Body Melanoma 30 5.987
93
UVL010 Uveal Disease 40 5.987
94
MLN002 Melanomatosis 26 5.987
95
HLX001 Helix Syndrome 47 3.912
96
PNG002 Pain Agnosia 51 3.736
97
NRN004 Neuroendocrine Tumor 55 3.213
98
PRT037 Pertussis 49 2.743
99
47X002 47,xyy 47 2.638
100
P TYR004 Tyrosinemia 49 2.588
101
P BRS047 Breast Cancer 97 2.459
102
HMN044 Human Immunodeficiency Virus Type 1 76 2.423
103
RPD005 Rapidly Involuting Congenital Hemangioma 48 2.380
104
PHN003 Phenylketonuria 76 2.233
105
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 2.065
106
P THL005 Thalassemia 56 2.005
107
P NRB001 Neuroblastoma 66 1.977
108
VCC001 Vaccinia 49 1.961
109
CYN002 Cyanosis, Transient Neonatal 43 1.869
110
HMG005 Hemoglobinopathy 55 1.848
111
P MYC084 Mycobacterium Tuberculosis 1 68 1.846
112
ALL029 Allergic Disease 61 1.770
113
P PNC035 Pancreatic Cancer 87 1.749
114
SVR004 Severe Combined Immunodeficiency 70 1.749
115
c ERY064 Erythrocytosis, Familial, 6 30 1.669
116
IMM167 Immune Deficiency Disease 76 1.648
117
P FBR017 Fibrosarcoma 55 1.571
118
48X005 48,xyyy 39 1.571
119
P PHC003 Pheochromocytoma 70 1.557
120
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.548
121
AMN003 Amnestic Disorder 53 1.519
122
c BSL024 Basal Cell Carcinoma 1 55 1.504
123
CYT002 Cytokine Deficiency 43 1.486
124
P AMY004 Amyloidosis 69 1.478
125
c ALP101 Alpha-Thalassemia 62 1.452
126
INS024 Insulin-Like Growth Factor I 77 1.449
127
c PCH010 Pachyonychia Congenita 3 43 1.437
128
c NRP064 Neuropathy, Congenital Hypomyelinating, 2 35 1.428
129
c BTT014 Beta-Thalassemia 72 1.424
130
GLM045 Glioma 62 1.412
131
GLL048 Glial Tumor 51 1.389
132
HRW001 Hair Whorl 35 1.385
133
HYP141 Hyperphenylalaninemia 42 1.361
134
ADR040 Adrenal Gland Pheochromocytoma 45 1.354
136
P PLY018 Polycythemia 56 1.314
137
c ACT027 Acute Pancreatitis 60 1.297
138
c PNC108 Pancreatitis, Hereditary 68 1.277
139
THY029 Thyroid Carcinoma 55 1.277
140
P BCL017 B-Cell Lymphoma 57 1.255
141
PST092 Posttransplant Acute Limbic Encephalitis 29 1.248
142
ATM095 Autoimmune Disease 61 1.240
143
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 1.233
144
IFP003 Ifap Syndrome 2 41 1.225
145
c HMC039 Hemochromatosis, Type 1 73 1.176
146
SQM006 Squamous Cell Carcinoma 59 1.176
147
P RTN024 Retinoblastoma 72 1.168
148
CHL014 Cholera 62 1.165
149
c MCR120 Microvascular Complications of Diabetes 7 47 1.159
150
c OST163 Osteopetrosis, Autosomal Recessive 3 54 1.142
151
P HML002 Hemolytic Anemia 62 1.142
152
STM007 Stomatitis 52 1.140
153
c MCR133 Microvascular Complications of Diabetes 4 41 1.131
154
c MCR113 Microvascular Complications of Diabetes 3 52 1.131
155
c MCR130 Microvascular Complications of Diabetes 6 41 1.131
156
TXC005 Toxic Shock Syndrome 61 1.131
157
P RTN016 Retinal Degeneration 52 1.131
158
c HPT073 Hepatitis C Virus 70 1.117
159
P PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 54 1.107
160
KRN002 Kearns-Sayre Syndrome 62 1.107
161
c CHR095 Chronic Progressive External Ophthalmoplegia 48 1.107
162
P PNC044 Pancreatitis 61 1.105
163
P LVR013 Liver Disease 68 1.104
164
CLT003 Colitis 63 1.101
165
BNR002 Bone Resorption Disease 47 1.091
166
OPT003 Opiate Dependence 49 1.090
167
c HRD039 Hereditary Amyloidosis 45 1.090
168
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 49 1.086
169
c PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 52 1.086
170
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 1.085
171
THY111 Thyroid Carcinoma, Familial Medullary 67 1.078
172
P HRP006 Herpes Simplex 65 1.078
173
ALK013 Alkaptonuria 58 1.073
174
CRB004 Cerebral Artery Occlusion 45 1.071
175
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 59 1.068
176
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.056
177
PRP030 Purpura 54 1.056
178
IMP004 Impetigo 48 1.056
179
HMG024 Hemoglobinopathy Toms River 13 1.056
180
ARG004 Argyria 26 1.050
181
P LKM071 Leukemia, Chronic Lymphocytic 74 1.044
182
THY125 Thyroid Gland Medullary Carcinoma 48 1.043
183
HMP009 Haemophilus Influenzae 41 1.036
184
P HMG032 Hemoglobin H Disease 51 1.036
185
P MLT074 Multiple Endocrine Neoplasia 58 1.006
186
P BRN019 Bernard-Soulier Syndrome 61 1.004
187
P MYP004 Myopathy 67 1.004
188
c SPN225 Spondyloarthropathy 1 70 0.998
189
SPN051 Spondylitis 51 0.998
190
INF009 Inflammatory Spondylopathy 30 0.998
191
TTN003 Tetanus 64 0.991
192
SRC014 Sarcoma 64 0.991
193
SPN035 Spindle Cell Sarcoma 51 0.974
194
CRC006 Carcinoid Syndrome 55 0.974
195
ART006 Arthus Reaction 40 0.974
196
P RHM011 Rheumatoid Arthritis 81 0.957
197
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.956
198
PRT251 Proteinuria, Chronic Benign 58 0.949
199
P PRG013 Paraganglioma 57 0.949
200
GST030 Gastrinoma 45 0.949
201
P ADN016 Adenocarcinoma 63 0.949
202
MSL001 Measles 61 0.949
203
ZLL002 Zollinger-Ellison Syndrome 55 0.940
204
P ART022 Arthritis 70 0.940
205
P MTH007 Methemoglobinemia 46 0.939
206
P SPN052 Spondyloarthropathy 54 0.931
207
BTT017 Beta-Thalassemia Major 54 0.919
208
c MGR028 Migraine with or Without Aura 1 63 0.912
209
P MYL006 Myeloid Leukemia 60 0.912
210
ORL015 Oral Squamous Cell Carcinoma 43 0.902
211
c ERY065 Erythrocytosis, Familial, 7 35 0.896
212
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.892
213
RNL077 Renal Fibrosis 46 0.892
214
P HYP086 Hypothyroidism 68 0.892
215
HYP056 Hypoglycemia 65 0.892
216
P MDL005 Medulloblastoma 75 0.882
217
P NSP012 Nasopharyngeal Carcinoma 60 0.882
218
c LKM063 Leukemia, Chronic Myeloid 70 0.882
219
P CTR002 Cataract 59 0.882
221
MLR004 Malaria 77 0.872
222
c PRC016 Pre-Eclampsia 64 0.872
223
P NRP001 Neuropathy 59 0.872
224
CRC014 Carcinoid Tumors, Intestinal 46 0.861
225
BCT022 Bacterial Infectious Disease 55 0.861
226
ORL011 Oral Cancer 60 0.861
227
SYN120 Syndromic Oculocutaneous Albinism 21 0.861
228
P BLD134 Bladder Cancer 79 0.849
229
CLN015 Colon Adenocarcinoma 64 0.849
230
GSG001 Gas Gangrene 52 0.849
231
WTH001 Withdrawal Disorder 47 0.838
232
PNC129 Pancreatic Adenocarcinoma 64 0.838
233
P SPP010 Suppressor of Tumorigenicity 3 50 0.826
234
P HPT023 Hepatocellular Carcinoma 95 0.826
235
NNL006 Non-Alcoholic Steatohepatitis 54 0.826
236
P INF037 Inflammatory Bowel Disease 53 0.813
237
P PRC019 Precocious Puberty 48 0.800
238
KRT002 Keratomalacia 54 0.788
240
c HNT011 Huntington Disease-Like 3 33 0.786
241
c MLT160 Multiple Endocrine Neoplasia, Type Iia 67 0.786
242
P PRP019 Peripheral Nervous System Disease 57 0.786
243
MDD011 Mood Disorder 61 0.786
244
ULC004 Ulcerative Colitis 74 0.786
245
OCL016 Ocular Albinism, X-Linked 24 0.786
246
P LNG028 Long Qt Syndrome 63 0.771
247
NRR001 Neuroretinitis 42 0.771
248
MRP001 Morphine Dependence 41 0.771
249
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.771
250
P RTN018 Retinal Disease 53 0.771
251
RTN023 Retinitis 45 0.771
252
P GLC113 Galactosemia I 65 0.755
253
RCT015 Reactive Arthritis 60 0.755
254
P PLY019 Polyneuropathy 52 0.755
255
OPD006 Opioid Addiction 48 0.755
256
P GLY013 Glycogen Storage Disease 59 0.738
257
RCK004 Rickets 64 0.738
258
c ACT134 Acute Liver Failure 57 0.738
259
P ALZ034 Alzheimer Disease 87 0.724
260
CRZ001 Crouzon Syndrome 64 0.720
261
PRC038 Precocious Puberty, Male-Limited 61 0.720
262
LPT001 Leptospirosis 65 0.720
263
PLM010 Pulmonary Edema 54 0.720
264
PLG002 Plague 58 0.720
265
SPL018 Splenomegaly 47 0.720
266
CRN294 Carnitine Palmitoyltransferase Ii Deficiency, Myopathic, Stress-Induced 31 0.700
267
PLY001 Polycythemia Vera 69 0.700
268
TBL029 Tubulin, Beta 28 0.700
269
CRN296 Carnitine Palmitoyltransferase Ii Deficiency, Infantile 64 0.700
270
HST010 Histiocytosis 49 0.700
271
FBR002 Fibrosarcoma of Bone 47 0.700
272
P THR005 Thrombotic Thrombocytopenic Purpura 64 0.700
273
HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 61 0.700
274
BRN053 Bronchial Adenomas/carcinoids Childhood 21 0.700
275
P HYP750 Hypertriglyceridemia, Familial 61 0.677
276
FRN006 Frontotemporal Dementia 68 0.677
277
P RSP003 Respiratory Failure 73 0.677
278
BRN028 Brain Cancer 73 0.677
279
P LNG032 Lung Cancer 98 0.660
280
GLB002 Glioblastoma 67 0.660
281
P PRK101 Parkinsonism-Dystonia, Infantile, 1 40 0.650
282
P PRP034 Purpura Fulminans 41 0.650
283
THR024 Thrombosis 56 0.650
284
ANT018 Anthracosis 50 0.650
285
P PNM006 Pneumoconiosis 55 0.650
286
KRT009 Keratosis 52 0.650
287
RSP023 Rasopathy 54 0.650
288
P HYP050 Hyperinsulinemic Hypoglycemia 56 0.650
289
P NRF002 Neurofibromatosis 60 0.650
290
GST050 Gastrointestinal System Disease 55 0.650
291
P HYP265 Hypotonia 42 0.650
292
PPL052 Papillomatosis, Confluent and Reticulated 34 0.648
293
HYP266 Hypoxia 56 0.648
294
OST159 Osteogenic Sarcoma 66 0.619
295
c ALZ056 Alzheimer Disease 3 56 0.614
296
ATR057 Atrioventricular Block 54 0.614
297
c GLY008 Glycogen Storage Disease Ii 72 0.614
298
P PLY006 Polydactyly 58 0.614
299
PNL019 Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities 54 0.614
300
c CNG223 Congenital Methemoglobinemia 39 0.614
301
c MLN040 Melanoma, Cutaneous Malignant 7 18 0.614
302
c SKN060 Skin/hair/eye Pigmentation, Variation in, 11 16 0.614
303
P ACN016 Acne Inversa, Familial, 3 28 0.614
304
PCK003 Pick Disease of Brain 70 0.614
305
c MCR115 Microvascular Complications of Diabetes 5 65 0.614
307
c AMY060 Amyloidosis, Primary Localized Cutaneous, 1 35 0.614
308
IMM165 Immunoglobulin Switch Sequences 14 0.614
309
P CRB045 Cerebellar Hypoplasia 40 0.614
310
ERY007 Erythropoietin Polycythemia 14 0.614
311
P BRD002 Bardet-Biedl Syndrome 66 0.614
312
IMM185 Immunodeficiency 26 with or Without Neurologic Abnormalities 31 0.614
313
c BRD047 Bardet-Biedl Syndrome 16 46 0.614
314
PRT011 Protein C Deficiency 47 0.614
315
c PRM012 Primary Polycythemia 58 0.614
316
P NPH005 Nephronophthisis 59 0.614
317
NNN026 Noonan Syndrome with Multiple Lentigines 64 0.614
318
MYC013 Mycobacterium Abscessus 42 0.614
320
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 0.614
321
LCH014 Lichen Amyloidosis 29 0.614
322
HYP060 Hyperinsulinism 53 0.613
323
INS001 Insulinoma 59 0.576
324
c HRM005 Hermansky-Pudlak Syndrome 1 55 0.557
325
ADN018 Adenoma 58 0.557
326
P SZR006 Seizure Disorder 69 0.543
327
CNT105 Central Core Disease of Muscle 59 0.528
328
P KRT028 Keratitis-Ichthyosis-Deafness Syndrome, Autosomal Dominant 54 0.528
329
c MLG147 Malignant Hyperthermia 1 47 0.528
330
TQP001 Taqi Polymorphism 29 0.528
331
FCT007 Factor Vii Deficiency 64 0.528
332
DYS165 Dysfibrinogenemia, Congenital 52 0.528
333
P CNT009 Central Core Myopathy 44 0.528
334
CLL014 Cll/sll 45 0.528
335
P BRT004 Bartter Disease 58 0.528
336
P MLG056 Malignant Hyperthermia 65 0.528
337
GST057 Gastro-Enteropancreatic Neuroendocrine Tumor 16 0.528
339
c TYP009 Type 2 Diabetes Mellitus 91 0.501
340
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.501
341
P SCK005 Sickle Cell Disease 56 0.501
342
P LKM062 Leukemia, Acute Lymphoblastic 69 0.493
343
c HYP836 Hypercholesterolemia, Familial, 1 73 0.493
344
ACT098 Acute Erythroid Leukemia 55 0.493
345
c HPT001 Hepatitis C 61 0.486
346
P LKM002 Leukemia 65 0.478
347
P PRS040 Prostate Cancer 95 0.470
348
MNN043 Meningioma, Familial 79 0.470
349
c PRM032 Primary Congenital Glaucoma 40 0.462
350
P GLM040 Glioma Susceptibility 1 70 0.462
351
MYL009 Myelodysplastic Syndrome 67 0.454
352
c SML038 Small Cell Cancer of the Lung 68 0.454
353
c GLC097 Glaucoma 3, Primary Congenital, a 58 0.454
354
ISC004 Ischemia 61 0.454
355
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.446
356
P OST002 Osteoporosis 76 0.446
357
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.446
358
LVR012 Liver Cirrhosis 62 0.446
359
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.446
360
SVR001 Severe Acute Respiratory Syndrome 68 0.446
361
SCR001 Secretory Meningioma 40 0.446
362
INT395 Intracranial Meningioma 47 0.446
363
P ENC018 Encephalopathy 62 0.446
364
P WSK001 Wiskott-Aldrich Syndrome 72 0.438
365
MLG169 Malignant Astrocytoma 57 0.438
366
P CLR023 Colorectal Cancer 100 0.429
367
P DBT005 Diabetes Insipidus 54 0.429
368
c LKM061 Leukemia, Acute Myeloid 83 0.421
369
P MYC007 Myocardial Infarction 69 0.421
370
HGH043 High Grade Glioma 46 0.421
371
P CRD246 Cardiovascular System Disease 55 0.421
372
ACQ007 Acquired Immunodeficiency Syndrome 58 0.421
373
AGN016 Aging 53 0.412
374
P GST053 Gastric Cancer 82 0.412
375
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.412
376
P VSC007 Vascular Disease 62 0.412
377
HYP066 Hyperglycemia 60 0.412
378
PTT037 Pituitary Tumors 44 0.412
379
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.403
380
P LNG064 Lung Cancer Susceptibility 3 69 0.403
381
ACR007 Acromegaly 70 0.403
382
P HPT021 Hepatitis 68 0.403
383
P UVT001 Uveitis 57 0.403
384
P DBT009 Diabetes Mellitus 67 0.403
385
P INF038 Influenza 68 0.403
386
FTT001 Fatty Liver Disease 61 0.403
387
P OVR042 Ovarian Cancer 88 0.394
388
ESP021 Esophageal Cancer 84 0.394
389
HPT004 Hepatic Coma 43 0.394
390
c THY107 Thymoma, Familial 42 0.384
391
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.384
392
HPT019 Hepatic Encephalopathy 59 0.384
393
P THY023 Thymoma 64 0.384
394
P GST044 Gastritis 55 0.384
395
RHB001 Rhabdoid Cancer 68 0.384
396
CYS001 Cystic Fibrosis 77 0.374
397
P PRK057 Parkinson Disease, Late-Onset 79 0.374
398
GLC003 Glucose Intolerance 53 0.374
399
MLD011 Mild Hyperphenylalaninemia 24 0.374
400
P MPL001 Maple Syrup Urine Disease 69 0.364
401
P ATX030 Ataxia-Telangiectasia 80 0.364
402
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.364
403
c HYP595 Hypertension, Essential 84 0.364
404
TLN003 Telangiectasis 51 0.364
405
CHR074 Choriocarcinoma 46 0.364
406
ILS001 Ileus 49 0.364
407
CLS049 Classic Phenylketonuria 34 0.364
408
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.354
409
MYL069 Myeloma, Multiple 76 0.354
410
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.354
411
P HYP069 Hyperparathyroidism 62 0.354
412
CHL068 Cholestasis 61 0.354
413
P LTR001 Lateral Sclerosis 57 0.354
414
P RHN004 Rhinitis 56 0.354
415
ANT024 Anthrax Disease 57 0.354
416
ALL014 Allergic Encephalomyelitis 34 0.354
417
FML292 Familial Drusen 34 0.354
418
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 49 0.343
419
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.343
420
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.343
421
HMC014 Homocysteinemia 52 0.343
422
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.343
423
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.343
424
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.343
425
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.343
426
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.343
427
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.343
428
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.343
429
P OST001 Osteopetrosis 70 0.343
430
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.343
431
PST011 Pustulosis of Palm and Sole 52 0.343
432
P PSR002 Psoriasis 63 0.343
434
INT029 Interleukin-7 Receptor Alpha Deficiency 27 0.333
435
P LYM118 Lymphoma 66 0.333
436
BSL037 Basal Laminar Drusen 41 0.333
437
HYP561 Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness 26 0.333
438
CHL123 Chlamydia 58 0.333
439
DPH001 Diphtheria 59 0.333
440
MYL031 Myeloproliferative Neoplasm 66 0.333
441
P DRR001 Diarrhea 55 0.333
442
CNS004 Constipation 56 0.333
443
MNT002 Mental Depression 56 0.333
444
MCH006 Mechanical Strabismus 40 0.333
445
END086 End Stage Renal Disease 54 0.333
446
PRT036 Peritonitis 65 0.333
447
c BCT007 Bacterial Meningitis 55 0.333
448
P MNN013 Meningitis 65 0.333
449
P MSC005 Muscular Dystrophy 66 0.333
450
PNM013 Pneumococcal Meningitis 43 0.333
451
P CHR345 Chronic Pain 50 0.333
452
c BRN108 Branchiootic Syndrome 1 63 0.321
453
c TYR013 Tyrosinemia, Type Ii 48 0.321
454
P MYS003 Myasthenia Gravis 67 0.321
455
GST019 Gastrointestinal Stromal Tumor 78 0.321
456
P KLZ004 Kala-Azar 1 41 0.321
457
PPL022 Papilloma 53 0.321
458
P PNM007 Pneumonia 64 0.321
459
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.321
460
SQM002 Squamous Cell Papilloma 45 0.321
461
GTR002 Goiter 52 0.321
462
P VNW001 Von Willebrand's Disease 64 0.321
463
P MCR010 Microcephaly 59 0.321
464
P PRN023 Prion Disease 60 0.321
465
LSH001 Leishmaniasis 63 0.321
466
SFT003 Soft Tissue Sarcoma 43 0.321
467
DPR016 Depression 64 0.321
468
ALL003 Allergic Rhinitis 66 0.310
469
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.310
470
c HRM008 Hermansky-Pudlak Syndrome 5 46 0.310
471
KRT019 Keratitis, Hereditary 66 0.310
472
CHL065 Cholangiocarcinoma 57 0.310
473
P TBR001 Tuberous Sclerosis 69 0.310
474
c FML021 Familial Hypercholesterolemia 71 0.310
475
c HPT016 Hepatitis B 62 0.310
476
INT079 Intrahepatic Cholangiocarcinoma 51 0.310
477
CMB007 Combined Immunodeficiency 56 0.297
478
HYP080 Hypogonadism 49 0.297
479
P DYS154 Dystonia 64 0.297
480
THY123 Thyroid Gland Follicular Carcinoma 53 0.297
481
EMB004 Embryonal Carcinoma 55 0.297
482
P BRS044 Breast Adenocarcinoma 58 0.297
483
P TRC031 Trichorhinophalangeal Syndrome 37 0.297
484
OST012 Osteoarthritis 77 0.297
485
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.297
486
ALC007 Alcohol Dependence 65 0.285
487
c TBR025 Tuberous Sclerosis 1 84 0.285
488
c ALB017 Albinism, Oculocutaneous, Type Vi 30 0.285
489
LNT004 Lentigines 45 0.285
490
ATY005 Atypical Teratoid Rhabdoid Tumor 69 0.285
491
P GLM007 Glomerulonephritis 59 0.285
492
P PTT006 Pituitary Adenoma 55 0.285
493
P RHB003 Rhabdomyosarcoma 66 0.285
494
LMY002 Leiomyoma 51 0.285
495
CHG001 Chagas Disease 65 0.285
496
c ACT075 Acute Myocardial Infarction 55 0.285
497
c MJR022 Major Affective Disorder 8 37 0.272
498
P CRN300 Coronary Heart Disease 1 73 0.272
499
P SCH015 Schizophrenia 74 0.272
500
c MJR024 Major Affective Disorder 9 40 0.272
501
c HRM009 Hermansky-Pudlak Syndrome 6 46 0.272
502
ANR007 Anorexia Nervosa 59 0.272
503
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.272
504
BRK010 Burkitt Lymphoma 65 0.272
505
c LNG109 Lung Cancer Susceptibility 1 26 0.272
506
CRV035 Cervical Cancer 72 0.272
507
P BPL003 Bipolar Disorder 56 0.272
508
TYP007 Typhoid Fever 63 0.272
509
PLM031 Poliomyelitis 62 0.272
510
P MST009 Mastocytosis 64 0.272
511
P ENC004 Encephalitis 61 0.272
512
VSC003 Visceral Leishmaniasis 54 0.272
513
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.272
514
P THY032 Thyroiditis 56 0.272
515
c CHR684 Chronic Kidney Disease 73 0.272
516
c LKM005 Leukemia, T-Cell, Chronic 33 0.272
517
MST020 Mast Cell Activation Syndrome 27 0.272
518
FCS014 Fucosidase Regulator 15 0.258
519
P CHN012 Chondrosarcoma 56 0.258
520
KPS004 Kaposi Sarcoma 76 0.258
521
c HMP004 Hemophilia B 68 0.258
522
P MJR001 Major Depressive Disorder 68 0.258
523
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.258
524
P HYP726 Hypercalcemia, Infantile, 1 58 0.258
525
P CRN037 Craniosynostosis 67 0.258
526
IRN002 Iron Metabolism Disease 56 0.258
527
THY030 Thyroid Gland Disease 50 0.258
528
SLP001 Sleeping Sickness 56 0.258
529
PPT005 Peptic Ulcer Disease 58 0.258
530
P HMP007 Hemophilia 52 0.258
531
P HDC001 Headache 56 0.258
532
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.243
533
c HYP807 Hyperinsulinemic Hypoglycemia, Familial, 6 52 0.243
534
P CLC063 Celiac Disease 1 65 0.243
535
P THN009 Thanatophoric Dysplasia, Type I 62 0.243
536
c PRS097 Prostate Cancer, Hereditary, 1 38 0.243
537
ANX010 Anxiety 70 0.243
538
P PLM037 Pulmonary Hypertension 69 0.243
539
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 0.243
540
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.243
541
ABT001 Abetalipoproteinemia 68 0.243
542
P AST005 Asthma 75 0.243
543
c HRM007 Hermansky-Pudlak Syndrome 4 46 0.243
544
P PRK039 Parkinsonism 55 0.243
545
CLR108 Colorectal Adenoma 63 0.243
546
P ALC033 Alcohol Use Disorder 67 0.243
547
MST004 Mast Cell Neoplasm 41 0.243
548
P PLY011 Polycystic Ovary Syndrome 57 0.243
549
AVN001 Avian Influenza 61 0.243
550
EXT007 Extracutaneous Mastocytoma 38 0.243
551
URM002 Uremia 47 0.243
552
PRT013 Portal Hypertension 59 0.243
553
CHR073 Choreatic Disease 53 0.243
554
GT001 Gout 63 0.243
555
BRN024 Bronchitis 67 0.243
556
c HPT007 Hepatitis E 50 0.243
557
P ATR005 Atrophic Gastritis 50 0.243
558
ETN001 Eating Disorder 59 0.243
559
CHR178 Chromosomal Triplication 33 0.243
560
TRN049 Transient Tyrosinemia of the Newborn 8 0.243
561
BRN071 Brain Injury 50 0.243
562
DWN001 Down Syndrome 70 0.227
563
PPL048 Papillorenal Syndrome 58 0.227
564
OCL069 Ocular Motor Apraxia 57 0.227
565
STR067 Stroke, Ischemic 79 0.227
566
MSC007 Muscle Hypertrophy 64 0.227
567
FDB001 Foodborne Botulism 55 0.227
568
c TYP008 Type 1 Diabetes Mellitus 77 0.227
569
JVN004 Juvenile Myelomonocytic Leukemia 66 0.227
570
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.227
571
P TMR010 Tumor Predisposition Syndrome 69 0.227
572
c ATR087 Atrial Standstill 1 74 0.227
573
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.227
574
P ANP001 Anaplastic Large Cell Lymphoma 59 0.227
575
P LYM033 Lymphoproliferative Syndrome 59 0.227
576
CLR109 Colorectal Adenocarcinoma 50 0.227
577
GST023 Gastric Ulcer 52 0.227
578
P DDN001 Duodenal Ulcer 52 0.227
579
CLN003 Clonorchiasis 42 0.227
580
OST015 Osteochondrodysplasia 60 0.227
581
FDL002 Food Allergy 47 0.227
582
P BNG032 Benign Mesothelioma 53 0.227
583
EXC002 Exocrine Pancreatic Insufficiency 42 0.227
584
P HYP730 Hypogonadotropic Hypogonadism 57 0.227
585
P CHR285 Chronic Myelomonocytic Leukemia 59 0.227
586
BRN004 Brain Edema 54 0.227
587
LPD008 Lipid Metabolism Disorder 61 0.227
588
LCH001 Leech Infestation 37 0.227
589
HYP005 Hypokalemia 55 0.227
590
P SYS005 Systemic Scleroderma 73 0.227
591
P ART023 Arthropathy 59 0.227
592
SKN020 Skin Papilloma 40 0.227
593
P CHR012 Chronic Granulomatous Disease 69 0.227
594
c PRM005 Primary Hyperparathyroidism 59 0.227
595
P RNL007 Renal Tubular Acidosis 52 0.227
596
NRN001 Neuroendocrine Carcinoma 47 0.227
597
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 0.227
598
LNG031 Lung Benign Neoplasm 51 0.227
599
P MSC003 Muscular Atrophy 52 0.227
600
GLC036 Glucagonoma 45 0.227
601
CND006 Candida Glabrata 29 0.227
602
SPN119 Spondylarthropathy 37 0.227
605
BLT023 Bilateral Acute Depigmentation of the Iris 18 0.227
606
INH023 Inherited Cancer-Predisposing Syndrome 53 0.227
607
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.210
608
ACH004 Achondroplasia 65 0.210
609
CHR105 Choreoacanthocytosis 55 0.210
610
DLT018 Dilution, Pigmentary 27 0.210
611
P EST010 Esterase B 13 0.210
612
PLY150 Polykaryocytosis Inducer 29 0.210
613
P RTT002 Rett Syndrome 79 0.210
614
GST092 Gastroesophageal Reflux 59 0.210
615
P MLT020 Multiple Sclerosis 79 0.210
616
SPP011 Suppression of Tumorigenicity 12 61 0.210
617
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.210
618
ASK001 Askin's Tumor 31 0.210
619
FTL006 Fetal Alcohol Spectrum Disorder 43 0.210
620
CHR081 Choroideremia 58 0.210
621
APP015 Apparent Mineralocorticoid Excess 57 0.210
622
HYP020 Hyperprolactinemia 63 0.210
623
LGN006 Legionnaire Disease 52 0.210
624
P HNT016 Huntington Disease 73 0.210
625
CRT072 Creutzfeldt-Jakob Disease 67 0.210
626
DSS009 Disseminated Intravascular Coagulation 56 0.210
627
QFV001 Q Fever 61 0.210
628
END040 Endogenous Depression 54 0.210
629
VPM001 Vipoma 48 0.210
630
P HRT032 Heart Disease 84 0.210
631
MDD018 Middle East Respiratory Syndrome 44 0.210
632
P PLM036 Pulmonary Fibrosis 65 0.210
633
LRY018 Laryngeal Squamous Cell Carcinoma 47 0.210
634
P HYP061 Hypertrophic Cardiomyopathy 68 0.210
635
P THR014 Thrombocytopenia 66 0.210
636
LYM009 Lymphocytic Choriomeningitis 46 0.210
637
P INF032 Infertility 60 0.210
638
c INH020 Inherited Metabolic Disorder 47 0.210
639
ALL006 Allergic Asthma 55 0.210
640
AMN012 Aminoacidopathies 19 0.210
641
P MNC007 Monocytic Leukemia 48 0.210
642
HYP213 Hypomelanotic Disorder 23 0.210
643
INT007 Intermediate Coronary Syndrome 53 0.210
644
CHC001 Chickenpox 56 0.210
645
TTR005 Tetrahydrobiopterin Deficiency 49 0.210
646
DFF036 Differentiated Thyroid Carcinoma 51 0.210
647
SML019 Smallpox 55 0.210
648
IRR002 Irritable Bowel Syndrome 64 0.210
649
MYC005 Myocardial Stunning 45 0.210
650
ANX004 Anoxia 40 0.210
651
HRD223 Hereditary Melanoma 38 0.210
652
HMZ003 Homozygous Familial Hypercholesterolemia 60 0.210
653
c HMN021 Human T-Cell Leukemia Virus Type 1 46 0.210
654
MNG006 Monogenic Diabetes 45 0.210
655
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 0.210
656
c ATS007 Autism Spectrum Disorder 71 0.192
657
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 0.192
658
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.192
659
BLM002 Bulimia Nervosa 56 0.192
660
RTN017 Retinal Detachment 60 0.192
661
ATH013 Atherosclerosis Susceptibility 63 0.192
662
c VNW005 Von Willebrand Disease, Type 1 46 0.192
663
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.192
664
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.192
665
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.192
666
FCT001 Factor Viii Deficiency 61 0.192
667
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.192
668
c HMP029 Hemophilia a 69 0.192
669
LWC002 Lowe Oculocerebrorenal Syndrome 68 0.192
670
END057 Endometrial Cancer 76 0.192
671
OBS082 Obstructive Nephropathy 41 0.192
672
P BND020 Bone Disease 60 0.192
673
MNT001 Mantle Cell Lymphoma 65 0.192
674
PLC006 Placental Choriocarcinoma 38 0.192
675
ANK001 Ankylosis 50 0.192
676
BLD053 Blood Platelet Disease 51 0.192
677
P OLG002 Oligodendroglioma 66 0.192
678
c VRL010 Viral Hepatitis 52 0.192
679
BLR001 Biliary Atresia 55 0.192
680
P END044 Endometriosis 62 0.192
681
PLM001 Pulmonary Tuberculosis 69 0.192
682
MST005 Mastitis 52 0.192
683
JPN002 Japanese Encephalitis 61 0.192
684
PLS007 Plasmodium Falciparum Malaria 52 0.192
685
P GND004 Gonadal Dysgenesis 46 0.192
686
c 46X082 46,xy Sex Reversal 52 0.192
687
P DMN002 Dementia 65 0.192
688
SHG001 Shigellosis 61 0.192
689
SCB001 Scabies 49 0.192
690
GST040 Gastric Adenocarcinoma 66 0.192
691
P LCH002 Lichen Planus 54 0.192
692
PLM033 Pulmonary Embolism 58 0.192
693
P LPS004 Lupus Erythematosus 61 0.192
694
OVR094 Ovarian Epithelial Cancer 39 0.192
695
ORL013 Oral Lichen Planus 45 0.192
696
TRM010 Traumatic Brain Injury 50 0.192
697
HYP855 Hyperpigmentation of the Skin 25 0.192
698
c RNG015 Ring Chromosome 2 22 0.192
699
SPN186 Spinal Cord Injury 60 0.192
700
BRN137 Bronchial Neuroendocrine Tumor 29 0.192
701
TRC123 Trichohepatoneurodevelopmental Syndrome 27 0.172
702
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.172
703
P CRD119 Cardiac Arrest 68 0.172
704
ING001 Inguinal Hernia 59 0.172
705
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.172
706
P PNT019 Pontocerebellar Hypoplasia 45 0.172
707
HYP003 Hypermethioninemia 51 0.172
708
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.172
709
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.172
710
ALX003 Alexander Disease 61 0.172
711
LPM012 Lipomatosis, Multiple 59 0.172
712
c SYS001 Systemic Lupus Erythematosus 85 0.172
713
P NNN008 Noonan Syndrome 1 76 0.172
714
c SCH079 Schizophrenia 1 44 0.172
715
c SCL052 Scleroderma, Familial Progressive 60 0.172
716
P HYP605 Hyperphenylalaninemia, Bh4-Deficient, B 44 0.172
717
MCK005 Mckusick-Kaufman Syndrome 61 0.172
718
HYD038 Hydrops Fetalis, Nonimmune 57 0.172
719
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.172
720
DRM046 Dermal Ridges-off-the-End 20 0.172
721
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.172
722
CRD223 Cardiac Arrhythmia 63 0.172
723
c SPN395 Spinal Muscular Atrophy, Type Ii 55 0.172
724
GLC012 Galactosialidosis 55 0.172
725
MSC157 Muscular Dystrophy, Duchenne Type 78 0.172
726
P RTN209 Retinoschisis 1, X-Linked, Juvenile 60 0.172
727
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.172
728
P DRM053 Dermatitis, Atopic 65 0.172
729
SCK003 Sickle Cell Anemia 74 0.172
730
ALB024 Albinism, Ocular, Type I 37 0.172
731
c LYM150 Lymphatic Malformation 7 43 0.172
732
DSS032 Disease by Infectious Agent 55 0.172
733
HYP017 Hypophosphatemia 49 0.172
734
VRL003 Variola Major 43 0.172
735
P SML001 Small Cell Carcinoma 52 0.172
736
SRN001 Serine Deficiency 24 0.172
737
HSH003 Hashimoto Thyroiditis 60 0.172
738
P PLT029 Platelet Groups--Ko System 15 0.172
739
SDD001 Sudden Infant Death Syndrome 60 0.172
740
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.172
741
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 50 0.172
742
c THR092 Thrombophilia Due to Thrombin Defect 74 0.172
743
P GRF003 Graft-Versus-Host Disease 71 0.172
744
c PNT033 Pontocerebellar Hypoplasia, Type 10 37 0.172
745
GRN037 Granulomatosis with Polyangiitis 66 0.172
746
DYS192 Dystonia, Dopa-Responsive 56 0.172
747
HYP042 Hypochondroplasia 58 0.172
748
MLT157 Multiple System Atrophy 1 69 0.172
749
c SKN065 Skin/hair/eye Pigmentation, Variation in, 1 27 0.172
750
WST005 West Nile Virus 55 0.172
751
P MLT008 Multinodular Goiter 41 0.172
752
P FTL001 Fetal Alcohol Syndrome 55 0.172
753
LYM040 Lymphoblastic Lymphoma 53 0.172
754
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.172
755
OST003 Osteonecrosis 60 0.172
756
PLM005 Pleomorphic Lipoma 39 0.172
757
MGC001 Megacolon 48 0.172
758
P KRT005 Keratoacanthoma 47 0.172
759
P LRY044 Larynx Cancer 53 0.172
760
P MYT023 Myotonia Congenita 55 0.172
761
HMS001 Hemosiderosis 48 0.172
762
P ECL001 Eclampsia 52 0.172
763
P BNG030 Benign Ependymoma 51 0.172
764
MYL075 Myelodysplastic/myeloproliferative Neoplasm 51 0.172
765
URT010 Ureteral Obstruction 44 0.172
766
SMT003 Somatostatinoma 52 0.172
767
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.172
768
CLL010 Cellular Ependymoma 58 0.172
769
BRN040 Bronchus Adenoma 23 0.172
770
P EMB005 Embryonal Rhabdomyosarcoma 53 0.172
771
MSN004 Mesenchymal Cell Neoplasm 42 0.172
772
c INF023 Inflammatory Breast Carcinoma 48 0.172
773
GST045 Gastroenteritis 58 0.172
774
DSS008 Disease of Mental Health 74 0.172
775
MTH009 Mouth Disease 57 0.172
776
DMY004 Demyelinating Disease 50 0.172
777
P ADL010 Adult Respiratory Distress Syndrome 70 0.172
778
OST011 Osteomalacia 52 0.172
779
c ACT073 Acute Leukemia 59 0.172
780
P RNL015 Renal Hypertension 45 0.172
781
SCH014 Schistosomiasis 56 0.172
782
P HML001 Hemolytic-Uremic Syndrome 52 0.172
783
PRN009 Paranoid Schizophrenia 49 0.172
784
DYS015 Dysentery 49 0.172
785
CRB039 Cerebrovascular Disease 65 0.172
786
c JVN010 Juvenile Rheumatoid Arthritis 52 0.172
787
IRD001 Iridocyclitis 54 0.172
788
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.172
789
FND002 Fundus Dystrophy 54 0.172
790
P TXP001 Toxoplasmosis 59 0.172
791
P MTC069 Mitochondrial Disorders 57 0.172
792
P JVN042 Juvenile Retinoschisis 39 0.172
793
PRT058 Pure Autonomic Failure 58 0.172
794
c RNG021 Ring Chromosome 5 20 0.172
795
CNG562 Congenital Hypogonadotropic Hypogonadism 28 0.172
796
RFR003 Refractive Error 41 0.172
797
P FML187 Familial Hypertension 34 0.172
798
XLN247 X-Linked Congenital Retinoschisis 21 0.172
799
P RRH023 Rare Hereditary Hemochromatosis 52 0.172
800
HRD224 Hereditary Nonpolyposis Colon Cancer 51 0.172
801
c PSD047 Pseudo-Turner Syndrome 52 0.172
802
PST103 Postpartum Psychosis 31 0.172
803
GLM044 Glomerular Disease 34 0.172
804
MYC015 Mycobacterium Fortuitum 28 0.172
805
ONC003 Oncogenic Osteomalacia 42 0.172
806
MYT011 Myotonia 37 0.172
807
THR035 Thrombasthenia 48 0.172
808
NRM021 Neurometabolic Disorder Due to Serine Deficiency 15 0.172
809
P OVR082 Overgrowth Syndrome 41 0.172
810
DFC004 Deficiency Anemia 74 0.149
811
LTN004 Late-Onset Retinal Degeneration 59 0.149
812
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 41 0.149
813
c CHR371 Charcot-Marie-Tooth Disease, Dominant Intermediate C 43 0.149
814
PFF001 Pfeiffer Syndrome 77 0.149
815
PHS025 Phosphatase, Acid, of Tissues 28 0.149
816
c MLN067 Melanoma, Cutaneous Malignant 2 29 0.149
817
NRL016 Neural Tube Defects 80 0.149
818
PPL049 Papillon-Lefevre Syndrome 65 0.149
819
P PRP003 Porphyria Cutanea Tarda 66 0.149
820
HTR005 Heterochromia Iridis 22 0.149
821
c HYP272 Hypercholesterolemia, Familial, 3 46 0.149
822
P MCR129 Microvascular Complications of Diabetes 1 67 0.149
823
P CTR177 Citrullinemia, Type Ii, Adult-Onset 56 0.149
824
c 46X051 46,xy Sex Reversal 1 38 0.149
825
GND001 Gonadoblastoma 42 0.149
826
c JVN061 Juvenile Arthritis 56 0.149
827
HYP457 Hypertrophic Scars 42 0.149
828
ANG054 Angina Pectoris 65 0.149
829
c CNG006 Congenital Hypothyroidism 63 0.149
830
P FML011 Familial Adenomatous Polyposis 70 0.149
831
P BRC006 Brachydactyly 52 0.149
832
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.149
833
CTS011 Cutis Marmorata Telangiectatica Congenita 34 0.149
834
URT049 Urate Oxidase, Pseudogene 24 0.149
835
P CRP001 Carpal Tunnel Syndrome 65 0.149
836
VRG001 Variegate Porphyria 55 0.149
837
LMY014 Leiomyoma, Uterine 55 0.149
838
MYL013 Myeloperoxidase Deficiency 44 0.149
839
P GLN011 Glanzmann Thrombasthenia 1 66 0.149
840
P FRG001 Fragile X Syndrome 70 0.149
841
FBR012 Fabry Disease 71 0.149
842
THN010 Thanatophoric Dysplasia, Type Ii 44 0.149
843
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.149
844
c HRM006 Hermansky-Pudlak Syndrome 3 43 0.149
845
ACT209 Acatalasemia 44 0.149
846
TRN072 Transferrin Serum Level Quantitative Trait Locus 2 17 0.149
847
c THR023 Thrombophilia Due to Thrombomodulin Defect 24 0.149
848
c INC015 Inclusion Body Myopathy with Early-Onset Paget Disease with or Without Frontotemporal Dementia 2 33 0.149
849
MYP088 Myopathy, Tubular Aggregate, 2 29 0.149
850
P ASP006 Aspergillosis 71 0.149
851
P AMY084 Amyloidosis, Finnish Type 51 0.149
852
BLD166 Blood Group, Diego System 14 0.149
853
CMR002 Coumarin Resistance 59 0.149
854
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 57 0.149
855
IGR001 Ige Responsiveness, Atopic 58 0.149
856
c MST023 Mesothelioma, Malignant 56 0.149
857
c ART151 Aortic Aneurysm, Familial Abdominal, 2 13 0.149
858
c SKN070 Skin/hair/eye Pigmentation, Variation in, 8 15 0.149
859
HLC007 Helicobacter Pylori Infection 67 0.149
860
P ADL017 Adult T-Cell Leukemia 53 0.149
861
CHR005 Chorioamnionitis 50 0.149
862
DFF005 Diffuse Large B-Cell Lymphoma 55 0.149
863
P SNS001 Sensorineural Hearing Loss 60 0.149
864
P MMP001 Mumps 56 0.149
865
P RCT021 Rectum Cancer 54 0.149
866
P ART021 Arteriosclerosis 53 0.149
867
BLR008 Bilirubin Metabolic Disorder 57 0.149
868
P HMN010 Hemangioma 61 0.149
869
c ACT071 Acute Kidney Failure 60 0.149
870
CNT047 Contact Dermatitis 56 0.149
871
P EPD016 Epidermolysis Bullosa 53 0.149
872
IMP005 Impotence 52 0.149
873
HYP014 Hyperuricemia 51 0.149
874
CRB037 Cerebral Palsy 66 0.149
875
URT001 Urethritis 52 0.149
876
P MLN007 Male Infertility 56 0.149
877
BNS004 Bone Squamous Cell Carcinoma 35 0.149
878
P CRV031 Cervical Adenocarcinoma 48 0.149
879
CLR030 Clear Cell Renal Cell Carcinoma 53 0.149
880
FBR047 Fibromyalgia 57 0.149
881
P KDN018 Kidney Disease 71 0.149
882
P END033 Endocarditis 58 0.149
883
P PRP029 Porphyria 60 0.149
884
NWC001 Newcastle Disease 47 0.149
885
P KDN017 Kidney Cancer 60 0.149
886
INT013 Intramuscular Hemangioma 31 0.149
887
GNG008 Ganglioneuroblastoma 46 0.149
888
MYF001 Myofibroma 42 0.149
889
END041 Endometrial Adenocarcinoma 63 0.149
890
ADR005 Adrenal Carcinoma 58 0.149
891
LNG039 Lung Squamous Cell Carcinoma 57 0.149
892
PSY004 Psychotic Disorder 66 0.149
893
SNS003 Sensory Peripheral Neuropathy 51 0.149
894
c SCN007 Secondary Hyperparathyroidism 50 0.149
895
GLY031 Glycoproteinosis 49 0.149
896
P GRV001 Graves' Disease 54 0.149
897
GST033 Gestational Diabetes 60 0.149
898
P CHR071 Charcot-Marie-Tooth Disease 64 0.149
899
P OPN001 Open-Angle Glaucoma 55 0.149
900
c HPT003 Hepatitis a 63 0.149
901
c ACT068 Acute Cystitis 60 0.149
902
FLR002 Filariasis 55 0.149
903
P MGR001 Migraine Without Aura 48 0.149
904
P GLL022 Guillain-Barre Syndrome 59 0.149
905
c INC033 Inclusion Body Myopathy with Early-Onset Paget Disease of Bone with or Without Frontotemporal Dementia 2 26 0.149
906
CHL004 Cholelithiasis 48 0.149
907
CMM004 Common Variable Immunodeficiency 71 0.149
908
FLR001 Filarial Elephantiasis 59 0.149
909
OCL022 Ocular Melanoma 54 0.149
910
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.149
911
MTC005 Mitochondrial Metabolism Disease 44 0.149
912
PLC008 Placenta Disease 48 0.149
913
P MYT002 Myotonic Dystrophy 51 0.149
914
BBS001 Babesiosis 48 0.149
915
YLL002 Yellow Fever 61 0.149
916
CWP001 Cowpox 44 0.149
917
ORP003 Oropharynx Cancer 54 0.149
918
DBT010 Diabetic Neuropathy 54 0.149
919
P INS002 in Situ Carcinoma 52 0.149
920
VSC002 Vascular Dementia 59 0.149
921
ACT250 Acute Megakaryocytic Leukemia 63 0.149
922
CRH001 Crohn's Disease 80 0.149
923
P HYP076 Hyperthyroidism 53 0.149
924
P DST107 Distal Renal Tubular Acidosis 48 0.149
925
FML249 Familial Amyloidosis, Finnish Type 35 0.149
926
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.149
927
HRT015 Heritable Pulmonary Arterial Hypertension 46 0.149
928
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.149
929
PLY100 Polyploidy 36 0.149
930
THR123 Thrombotic Microangiopathy 40 0.149
931
ISL131 Isolated Foveal Hypoplasia 12 0.149
932
c RNG008 Ring Chromosome 13 31 0.149
933
CRB090 Cerebral Hypoxia 42 0.149
934
INF034 Infective Endocarditis 53 0.121
935
P RBN002 Robinow Syndrome 56 0.121
936
SQL002 Squalene Synthase Deficiency 27 0.121
937
BRN032 Brain Glioma 45 0.121
938
CRH005 Crohn's Colitis 53 0.121
939
P PTS002 Ptosis 52 0.121
940
P SLP006 Sleep Apnea 69 0.121
941
HPT067 Hepatocellular Adenoma 42 0.121
942
FBR054 Fibroma 44 0.121
943
TCK001 Tick-Borne Encephalitis 58 0.121
944
P LDD007 Liddle Syndrome 1 57 0.121
945
ART140 Arteries, Anomalies of 52 0.121
946
AFB002 Afibrinogenemia, Congenital 63 0.121
947
CTR172 Citrullinemia, Classic 64 0.121
948
P IGN003 Iga Nephropathy 1 39 0.121