Search results for actb

574 hits were found for actb

# Family MCID Name MIFTS Score
1
c BRT038 Baraitser-Winter Syndrome 1 41 47.443
2
BRT046 Baraitser-Winter Cerebrofrontofacial Syndrome 43 38.565
3
c DYS162 Dystonia, Juvenile-Onset 31 35.966
4
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 26.891
5
P BRT040 Baraitser-Winter Syndrome 34 21.786
6
DSS008 Disease of Mental Health 74 18.905
7
P MCR010 Microcephaly 60 17.953
8
P LKM062 Leukemia, Acute Lymphoblastic 69 16.513
9
CHL152 Childhood Acute Lymphocytic Leukemia 50 16.183
10
P DYS154 Dystonia 64 14.486
11
P CLR023 Colorectal Cancer 100 13.574
12
P HPT023 Hepatocellular Carcinoma 96 13.509
13
P BRS047 Breast Cancer 98 12.975
14
P GST053 Gastric Cancer 83 12.975
15
P PTS002 Ptosis 52 11.016
16
BCK005 Becker Nevus Syndrome 33 9.885
17
P BLD062 Bile Duct Cancer 67 9.727
18
P LSS002 Lissencephaly 50 9.547
19
P PRK057 Parkinson Disease, Late-Onset 80 9.168
20
P KDN017 Kidney Cancer 61 9.077
21
P SCH015 Schizophrenia 74 8.978
22
c AMY091 Amyotrophic Lateral Sclerosis 1 88 8.744
23
c DLT002 Dilated Cardiomyopathy 78 8.597
24
P HYP061 Hypertrophic Cardiomyopathy 69 8.597
25
CLN015 Colon Adenocarcinoma 65 8.597
26
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 8.405
28
EWN003 Ewing Sarcoma 70 8.405
29
P NNN008 Noonan Syndrome 1 77 8.405
30
P NRB001 Neuroblastoma 66 8.405
31
P CNR004 Cone-Rod Dystrophy 2 74 7.942
32
P FRD001 Friedreich Ataxia 61 7.942
33
c HYP595 Hypertension, Essential 85 7.942
34
P OPN001 Open-Angle Glaucoma 55 7.942
35
P BRD002 Bardet-Biedl Syndrome 66 7.942
36
P SKN015 Skin Carcinoma 71 7.942
37
P CTR002 Cataract 60 7.942
38
P OVR049 Ovarian Disease 52 7.942
39
MLG169 Malignant Astrocytoma 57 7.701
40
c LKM061 Leukemia, Acute Myeloid 83 6.926
41
c EXD008 Exudative Vitreoretinopathy 1 71 6.652
42
MYL069 Myeloma, Multiple 77 6.652
43
P RTN008 Retinitis Pigmentosa 80 6.418
44
7P2001 7p22.1 Microduplication Syndrome 17 6.271
45
P HRD011 Hereditary Spherocytosis 64 6.271
46
SPP011 Suppression of Tumorigenicity 12 61 6.079
47
PLM134 Pulmonary Fibrosis, Idiopathic 76 6.079
48
MLB001 Mulibrey Nanism 52 6.079
49
c RTN041 Retinitis Pigmentosa 11 42 6.079
50
OVR059 Ovary Adenocarcinoma 49 6.079
51
c CRD236 Cardiomyopathy, Familial Hypertrophic, 25 47 5.616
52
c SPN393 Spinal Muscular Atrophy, Type I 51 5.616
53
c RTN052 Retinitis Pigmentosa 23 37 5.616
54
c RTN053 Retinitis Pigmentosa 24 27 5.616
55
ECT070 Ectodermal Dysplasia 1, Hypohidrotic, X-Linked 60 5.616
56
WLS003 Wilson-Turner X-Linked Mental Retardation Syndrome 47 5.616
57
P PLZ001 Pelizaeus-Merzbacher Disease 65 5.616
58
c RTN047 Retinitis Pigmentosa 18 46 5.616
59
KGM001 Kagami-Ogata Syndrome 53 5.616
60
c LKM070 Leukemia, Acute Monocytic 56 5.616
61
PRM057 Paramyotonia Congenita of Von Eulenburg 59 5.616
62
CNT099 Contractural Arachnodactyly, Congenital 54 5.616
63
P LYS001 Loeys-Dietz Syndrome 65 5.616
64
RSP004 Respiratory System Benign Neoplasm 28 5.616
65
P DST002 Distal Arthrogryposis 65 5.616
66
ATS009 Autosomal Genetic Disease 25 5.616
67
XLN230 X-Linked Monogenic Disease 18 5.616
68
c CTR097 Cataract 34, Multiple Types 29 5.616
69
DRG013 Drug-Induced Lupus Erythematosus 49 5.616
70
ADS001 Adiaspiromycosis 29 5.616
71
RSP023 Rasopathy 53 5.616
72
P HYP700 Hypomyelinating Leukodystrophy 34 5.616
73
SPC003 Specific Developmental Disorder 29 5.616
74
c HRD007 Hereditary Lymphedema 34 5.616
75
PLM135 Palmoplantar Keratoderma, Bothnian Type 48 5.616
76
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 5.616
77
ODN023 Odontochondrodysplasia 67 5.616
78
c CRD065 Cardiomyopathy, Familial Hypertrophic, 2 47 5.616
79
c CTR103 Cataract 4, Multiple Types 48 5.616
80
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 5.616
81
c HYP507 Hypotrichosis 1 43 5.616
82
c PSR018 Psoriasis 13 52 5.616
83
c NPH056 Nephrolithiasis/osteoporosis, Hypophosphatemic, 1 41 5.616
84
c LYS018 Loeys-Dietz Syndrome 2 50 5.616
85
c AML044 Amelogenesis Imperfecta, Type Ig 53 5.616
86
P MTC003 Metachromatic Leukodystrophy 71 5.616
87
P KLN006 Koolen-De Vries Syndrome 51 5.616
88
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 69 5.616
89
KFM001 Kaufman Oculocerebrofacial Syndrome 55 5.616
90
c GNT049 Giant Axonal Neuropathy 1, Autosomal Recessive 48 5.616
91
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 69 5.616
92
c HYP525 Hypotrichosis 2 36 5.616
93
P KBK002 Kabuki Syndrome 1 65 5.616
94
HMT008 Hematuria, Benign Familial 54 5.616
95
c PRM023 Pre-Malignant Neoplasm 28 5.616
96
c ATS203 Autosomal Dominant Non-Syndromic Intellectual Disability 45 5.616
97
XLN228 X-Linked Recessive Disease 24 5.616
98
LBR036 Leber Plus Disease 66 5.616
99
c FTL072 Fetal Akinesia Deformation Sequence 4 37 5.616
100
c ATS013 Autosomal Recessive Congenital Ichthyosis 66 5.616
101
INT253 Intestinal Benign Neoplasm 46 5.616
102
c SBC010 Subacute Glomerulonephritis 21 5.616
103
LCN001 Lice Infestation 41 5.616
104
SKN019 Skin Melanoma 71 5.616
105
TXC002 Toxic Encephalopathy 52 5.616
106
FND002 Fundus Dystrophy 55 5.616
107
INT379 Integumentary System Disease 29 5.616
108
P HRD018 Hair Disease 44 5.616
109
P CNG001 Congenital Myasthenic Syndrome 68 5.616
110
GLC008 Glucose Metabolism Disease 40 5.616
111
THY123 Thyroid Gland Follicular Carcinoma 55 5.616
112
PRS033 Parasitic Ectoparasitic Infectious Disease 28 5.616
113
ACT055 Actinomycosis 55 5.616
114
OVR060 Ovary Epithelial Cancer 27 5.616
115
CRV040 Cervix Carcinoma 50 5.616
116
TTH005 Teeth Hard Tissue Disease 24 5.616
117
P AML002 Amelogenesis Imperfecta 56 5.616
118
P ATN003 Autonomic Nervous System Neoplasm 26 5.616
119
SPN369 Spinal Disease 44 5.616
120
c HRD202 Hereditary Lymphedema I 49 5.616
121
TNG004 Tongue Disease 43 5.616
122
c INH020 Inherited Metabolic Disorder 48 5.616
123
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 50 5.616
124
P EYD002 Eye Disease 57 5.616
125
P PRP019 Peripheral Nervous System Disease 58 5.616
126
SKN020 Skin Papilloma 40 5.616
127
MLG076 Malignant Ovarian Surface Epithelial-Stromal Neoplasm 26 5.616
128
CRB016 Carbuncle 39 5.616
129
CLN045 Colonic Benign Neoplasm 48 5.616
130
c CNG513 Congenital Ptosis 42 5.616
131
P PRP021 Peripheral Nervous System Neoplasm 38 5.616
132
P LNS003 Lens Disease 34 5.616
133
CRB033 Cerebral Degeneration 39 5.616
134
EYD001 Eye Degenerative Disease 25 5.616
135
P NRV007 Nervous System Disease 67 5.616
136
c BRN108 Branchiootic Syndrome 1 62 3.566
137
CLB010 Coloboma of Macula 53 3.124
138
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 2.769
139
HYP748 Hypertelorism 46 2.638
140
DWN001 Down Syndrome 70 2.525
141
P THR014 Thrombocytopenia 66 2.475
142
GLM045 Glioma 63 2.415
143
GLB002 Glioblastoma 67 2.406
144
P GLM040 Glioma Susceptibility 1 71 2.341
145
P CRN037 Craniosynostosis 68 2.277
146
HMN016 Hemangioendothelioma 34 2.261
147
STR067 Stroke, Ischemic 80 2.137
148
RNL114 Renal Cell Carcinoma, Nonpapillary 80 2.137
149
P MYC007 Myocardial Infarction 70 2.137
150
P MLN008 Melanoma 76 2.137
151
P HYP040 Hypospadias 51 2.137
152
P INF037 Inflammatory Bowel Disease 53 2.062
153
TBL029 Tubulin, Beta 28 1.910
154
P OVR042 Ovarian Cancer 88 1.907
155
HMH004 Hemihyperplasia, Isolated 41 1.898
156
P SCL018 Scoliosis 57 1.898
157
GLL048 Glial Tumor 52 1.898
158
IDP070 Idiopathic Scoliosis 42 1.898
159
HYP266 Hypoxia 57 1.853
160
P RRT020 Rare Tumor 39 1.807
161
ULC004 Ulcerative Colitis 74 1.807
162
P DMN002 Dementia 66 1.807
163
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 1.794
164
CLF027 Cleft Palate, Isolated 64 1.708
165
c BRT039 Baraitser-Winter Syndrome 2 26 1.708
166
MTH009 Mouth Disease 57 1.708
167
DFF016 Diffuse Astrocytoma 45 1.708
168
ANP005 Anaplastic Astrocytoma 57 1.708
169
ORL011 Oral Cancer 60 1.599
170
PCT003 Pectus Excavatum 46 1.599
171
DSS032 Disease by Infectious Agent 55 1.599
172
P ALZ034 Alzheimer Disease 87 1.536
173
P BLD134 Bladder Cancer 79 1.536
174
DBW001 Dubowitz Syndrome 48 1.475
175
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 1.475
176
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 1.475
177
SPN035 Spindle Cell Sarcoma 54 1.475
178
P SNS001 Sensorineural Hearing Loss 59 1.475
179
HND002 Hand, Foot and Mouth Disease 50 1.475
180
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 1.390
181
PCH002 Pachygyria 32 1.390
182
MYP064 Myopericytoma 29 1.327
183
ANG018 Angiomyolipoma 46 1.327
184
SRC014 Sarcoma 65 1.327
185
SFT003 Soft Tissue Sarcoma 57 1.327
186
FRG010 Fragile X Tremor/ataxia Syndrome 44 1.310
187
PPL052 Papillomatosis, Confluent and Reticulated 34 1.310
188
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 44 1.310
189
P MSC003 Muscular Atrophy 52 1.310
190
P TRM003 Tremor 48 1.310
191
GST040 Gastric Adenocarcinoma 67 1.310
192
c ACT073 Acute Leukemia 58 1.226
193
P INF038 Influenza 68 1.226
194
P PNC044 Pancreatitis 61 1.226
195
OVR094 Ovarian Epithelial Cancer 39 1.226
196
c TRC092 Trichorhinophalangeal Syndrome, Type I 54 1.136
197
P RHB003 Rhabdomyosarcoma 66 1.136
198
ASP037 Aspm Primary Microcephaly 10 1.136
199
c PRM212 Primary Microcephaly 40 1.136
200
P SZR006 Seizure Disorder 70 1.135
201
P ATX030 Ataxia-Telangiectasia 80 1.135
202
P PLM037 Pulmonary Hypertension 72 1.135
203
DFF005 Diffuse Large B-Cell Lymphoma 54 1.135
204
MNN043 Meningioma, Familial 79 1.135
205
RNL077 Renal Fibrosis 46 1.135
206
P BCL017 B-Cell Lymphoma 59 1.135
207
ART016 Aortic Aneurysm 68 1.135
208
CHL061 Childhood Leukemia 47 1.135
209
LNG099 Lung Disease 62 1.135
210
CMB007 Combined Immunodeficiency 57 1.135
211
TLN003 Telangiectasis 51 1.135
212
P SPN046 Spinal Muscular Atrophy 63 1.135
213
c ACT027 Acute Pancreatitis 60 1.135
214
P ADN016 Adenocarcinoma 63 1.135
215
SVR004 Severe Combined Immunodeficiency 72 1.135
216
AGN016 Aging 54 1.036
217
P BND018 Band Heterotopia 53 1.036
218
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 1.036
219
c MJR022 Major Affective Disorder 8 38 1.036
220
NNL006 Non-Alcoholic Steatohepatitis 54 1.036
221
P LYM118 Lymphoma 67 1.036
222
c MJR024 Major Affective Disorder 9 41 1.036
223
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 1.036
224
OST159 Osteogenic Sarcoma 66 1.036
225
P HNT016 Huntington Disease 73 1.036
226
P HRP006 Herpes Simplex 65 1.036
227
P EPL164 Epilepsy 68 1.036
228
P BPL003 Bipolar Disorder 56 1.036
229
LYM027 Lymphopenia 56 1.036
230
P LKM002 Leukemia 67 1.036
231
P AGM001 Agammaglobulinemia 68 1.036
232
P INF032 Infertility 57 1.036
233
RTN123 Retinochoroidal Coloboma 18 1.036
234
P PNC035 Pancreatic Cancer 86 0.980
235
ADN011 Adenoid Cystic Carcinoma 68 0.944
236
CRV013 Cervical Adenoid Cystic Carcinoma 33 0.944
237
P OVR082 Overgrowth Syndrome 49 0.927
238
P NSP012 Nasopharyngeal Carcinoma 61 0.927
239
P OST002 Osteoporosis 76 0.927
240
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.927
241
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.927
242
CLT003 Colitis 63 0.927
243
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.927
244
CHR072 Chordoma 57 0.927
245
P PRS040 Prostate Cancer 95 0.927
246
THY029 Thyroid Carcinoma 51 0.927
247
FTT001 Fatty Liver Disease 62 0.927
248
CLR030 Clear Cell Renal Cell Carcinoma 54 0.927
249
c CRT089 Cortical Dysplasia, Complex, with Other Brain Malformations 10 39 0.927
250
P END044 Endometriosis 62 0.927
251
P PLY011 Polycystic Ovary Syndrome 57 0.927
252
SQM006 Squamous Cell Carcinoma 60 0.927
253
TBL023 Tubulinopathies 31 0.927
254
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 0.857
255
P TRN020 Turner Syndrome 67 0.857
256
CLF004 Cleft Lip/palate 57 0.802
257
FNG016 Fungal Keratitis 39 0.802
258
CNG506 Congenital Amyoplasia 27 0.802
259
ART140 Arteries, Anomalies of 53 0.802
260
ATH013 Atherosclerosis Susceptibility 63 0.802
261
INS024 Insulin-Like Growth Factor I 78 0.802
262
AGM019 Agammaglobulinemia, X-Linked 72 0.802
263
P AST005 Asthma 76 0.802
264
c OPT053 Optic Atrophy 1 62 0.802
265
P MLT020 Multiple Sclerosis 79 0.802
266
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 0.802
267
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.802
268
LPP008 Lipoprotein Quantitative Trait Locus 65 0.802
269
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.802
270
KRT019 Keratitis, Hereditary 66 0.802
271
SNR002 Sener Syndrome 17 0.802
272
P SRC025 Sarcoidosis 1 71 0.802
273
PLY183 Polymicrogyria with or Without Vascular-Type Ehlers-Danlos Syndrome 41 0.802
274
NRR001 Neuroretinitis 42 0.802
275
TRM010 Traumatic Brain Injury 51 0.802
276
RTN023 Retinitis 46 0.802
277
CLF001 Cleft Lip 53 0.802
278
P MSC005 Muscular Dystrophy 67 0.802
279
HYP066 Hyperglycemia 61 0.802
280
P BRS044 Breast Adenocarcinoma 58 0.802
281
LNG039 Lung Squamous Cell Carcinoma 57 0.802
282
SCR001 Secretory Meningioma 40 0.802
283
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.802
284
P CRN024 Corneal Disease 44 0.802
285
CRB004 Cerebral Artery Occlusion 45 0.802
286
P LNG064 Lung Cancer Susceptibility 3 70 0.802
287
DNG001 Dengue Shock Syndrome 40 0.802
288
DNG003 Dengue Disease 65 0.802
289
P MLN007 Male Infertility 56 0.802
290
GTR002 Goiter 53 0.802
291
DNG002 Dengue Hemorrhagic Fever 60 0.802
292
P LTR001 Lateral Sclerosis 58 0.802
293
CRN027 Corneal Neovascularization 47 0.802
294
P BND020 Bone Disease 59 0.802
295
PRM013 Premature Menopause 58 0.802
296
INT066 Interstitial Lung Disease 60 0.802
297
P TMP001 Temporal Lobe Epilepsy 49 0.802
298
SPN021 Spinal Meningioma 50 0.802
299
STT001 Status Epilepticus 59 0.802
301
PLY024 Polymicrogyria 47 0.802
302
P NRF002 Neurofibromatosis 57 0.802
303
NRF007 Neurofibroma 64 0.802
304
P FBR031 Febrile Seizures 52 0.802
305
CLB009 Coloboma of Iris 25 0.802
306
SGM006 Segmental Odontomaxillary Dysplasia 13 0.672
307
P PLC011 Pilocytic Astrocytoma 57 0.672
308
P ATS364 Autism 69 0.655
309
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.655
310
PLY100 Polyploidy 36 0.655
311
P THL005 Thalassemia 56 0.655
312
P AVS003 Avascular Necrosis 41 0.655
313
PRS129 Prostatic Hyperplasia, Benign 49 0.655
314
FRN006 Frontotemporal Dementia 68 0.655
315
P WSK001 Wiskott-Aldrich Syndrome 72 0.655
316
CRD132 Cardiac Conduction Defect 60 0.655
317
ART002 Arts Syndrome 66 0.655
318
c LSS005 Lissencephaly 1 57 0.655
319
MSC157 Muscular Dystrophy, Duchenne Type 79 0.655
320
CRV035 Cervical Cancer 73 0.655
321
END057 Endometrial Cancer 72 0.655
322
PLY150 Polykaryocytosis Inducer 29 0.655
323
CRZ001 Crouzon Syndrome 65 0.655
324
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 0.655
325
P FML011 Familial Adenomatous Polyposis 71 0.655
326
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.655
327
P OMP004 Omphalocele 48 0.655
328
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.655
329
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.655
330
c TBR025 Tuberous Sclerosis 1 84 0.655
331
ESP021 Esophageal Cancer 83 0.655
332
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.655
333
ORL015 Oral Squamous Cell Carcinoma 43 0.655
334
TNG007 Tongue Carcinoma 52 0.655
335
RPD005 Rapidly Involuting Congenital Hemangioma 46 0.655
336
P AMY004 Amyloidosis 70 0.655
337
BRN004 Brain Edema 54 0.655
338
P MYP004 Myopathy 67 0.655
339
CRV002 Cervix Uteri Carcinoma in Situ 47 0.655
340
DGN001 Degenerative Disc Disease 49 0.655
341
P MYL006 Myeloid Leukemia 61 0.655
342
P MVM001 Movement Disease 61 0.655
343
P ALC033 Alcohol Use Disorder 61 0.655
344
P CHR012 Chronic Granulomatous Disease 69 0.655
345
HLX001 Helix Syndrome 48 0.655
346
P GRF003 Graft-Versus-Host Disease 71 0.655
347
OST003 Osteonecrosis 61 0.655
348
PRS021 Prostatic Adenoma 43 0.655
349
P NPH012 Nephrotic Syndrome 60 0.655
350
CHL014 Cholera 62 0.655
351
P TBR001 Tuberous Sclerosis 69 0.655
352
P INF049 Infantile Myofibromatosis 55 0.655
353
MST005 Mastitis 53 0.655
354
PRS045 Prostatic Hypertrophy 53 0.655
355
THY030 Thyroid Gland Disease 50 0.655
356
ISC004 Ischemia 61 0.655
357
P GLL018 Gallbladder Cancer 53 0.655
358
CYS002 Cystic Lymphangioma 45 0.655
359
MSN004 Mesenchymal Cell Neoplasm 42 0.655
360
P MTR014 Motor Neuron Disease 65 0.655
361
CHL122 Cholesteatoma of Middle Ear 51 0.655
362
c HPT016 Hepatitis B 62 0.655
363
P RCT021 Rectum Cancer 54 0.655
364
c ACT135 Acute Graft Versus Host Disease 51 0.655
365
P ENC004 Encephalitis 61 0.655
366
STM007 Stomatitis 54 0.655
367
P HYP265 Hypotonia 42 0.655
368
ANR040 Aneurysm 61 0.655
369
BRN071 Brain Injury 50 0.655
370
CNG065 Congenital Contractures 25 0.655
371
CRV045 Cervical Intraepithelial Neoplasia 39 0.655
372
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.517
373
P LNG032 Lung Cancer 98 0.463
374
ANX004 Anoxia 40 0.463
375
GRW007 Growth Hormone Deficiency 46 0.463
376
RFR010 Refractory Anemia 49 0.463
377
ITR003 Iatrogenic Creutzfeldt-Jakob Disease 15 0.463
378
SPN186 Spinal Cord Injury 61 0.463
379
OCL015 Oculomotor Apraxia 39 0.463
380
c OTP006 Otopalatodigital Syndrome, Type I 60 0.463
381
CMB081 Combined Immunodeficiency, X-Linked 38 0.463
382
P RTT002 Rett Syndrome 79 0.463
383
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.463
384
MST006 Mast Syndrome 40 0.463
385
c THY107 Thymoma, Familial 42 0.463
386
SRC027 Sarcoma, Synovial 58 0.463
387
FBR012 Fabry Disease 70 0.463
388
c AMY045 Amyotrophic Lateral Sclerosis 4, Juvenile 49 0.463
389
c RTN046 Retinitis Pigmentosa 17 37 0.463
390
P DRM053 Dermatitis, Atopic 65 0.463
391
c SPS151 Spastic Paraplegia 11, Autosomal Recessive 49 0.463
392
P MYC084 Mycobacterium Tuberculosis 1 68 0.463
393
c PLM164 Pulmonary Hypertension, Primary, 1 76 0.463
394
CRT072 Creutzfeldt-Jakob Disease 68 0.463
395
P CFF008 Coffin-Siris Syndrome 1 64 0.463
396
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.463
397
ATM095 Autoimmune Disease 61 0.463
398
GLL008 Gilles De La Tourette Syndrome 65 0.463
399
ALC007 Alcohol Dependence 66 0.463
400
P CLC063 Celiac Disease 1 66 0.463
401
CYS001 Cystic Fibrosis 78 0.463
402
c FNC027 Fanconi Anemia, Complementation Group a 81 0.463
403
c LKM063 Leukemia, Chronic Myeloid 71 0.463
404
CHR100 Chronic Ulcer of Skin 57 0.463
405
PRP027 Peripheral Vascular Disease 71 0.463
406
FML037 Female Breast Cancer 51 0.463
407
MNT001 Mantle Cell Lymphoma 67 0.463
408
c MCR115 Microvascular Complications of Diabetes 5 65 0.463
409
c MCR130 Microvascular Complications of Diabetes 6 41 0.463
410
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.463
411
c HYP544 Hypotrichosis 10 15 0.463
412
MYL009 Myelodysplastic Syndrome 67 0.463
413
c RTN129 Retinitis Pigmentosa 49 38 0.463
414
DTS001 Diets-Jongmans Syndrome 22 0.463
415
c ATS007 Autism Spectrum Disorder 72 0.463
416
CNN010 Connective Tissue Benign Neoplasm 44 0.463
417
END062 Endometrial Hyperplasia 48 0.463
418
JNS001 Janus Kinase-3 Deficiency 21 0.463
419
OST006 Osteoblastoma 38 0.463
420
APR001 Apraxia 52 0.463
421
P CRB045 Cerebellar Hypoplasia 40 0.463
422
BNR002 Bone Resorption Disease 47 0.463
423
CD4003 Cd40 Ligand Deficiency 54 0.463
424
CRH005 Crohn's Colitis 53 0.463
425
P PRV002 Periventricular Nodular Heterotopia 52 0.463
426
P FTL002 Fatal Familial Insomnia 50 0.463
427
c PRS122 Persistent Hyperplastic Primary Vitreous, Autosomal Recessive 38 0.463
428
IMM167 Immune Deficiency Disease 78 0.463
429
WVR001 Weaver Syndrome 56 0.463
430
SVR066 Severe Combined Immunodeficiency, X-Linked 66 0.463
431
P CRP001 Carpal Tunnel Syndrome 66 0.463
432
KPS004 Kaposi Sarcoma 77 0.463
433
IGR001 Ige Responsiveness, Atopic 59 0.463
434
c DPH024 Diaphragmatic Hernia, Congenital 64 0.463
435
P PRT008 Proteus Syndrome 63 0.463
436
RNL065 Renal Cell Carcinoma, Papillary, 1 79 0.463
437
OMN001 Omenn Syndrome 63 0.463
438
P SPN429 Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2 57 0.463
439
LGH019 Light Fixation Seizure Syndrome 27 0.463
440
LPT014 Leptin Deficiency or Dysfunction 78 0.463
441
CRP030 Corpus Callosum, Agenesis of, with Facial Anomalies and Cerebellar Ataxia 37 0.463
442
c PCH010 Pachyonychia Congenita 3 43 0.463
443
c HPT073 Hepatitis C Virus 71 0.463
444
ACT119 Acute Promyelocytic Leukemia 62 0.463
445
c MCR120 Microvascular Complications of Diabetes 7 47 0.463
446
MCR237 Macrocephaly/megalencephaly Syndrome, Autosomal Recessive 40 0.463
447
P NJM001 Nijmegen Breakage Syndrome 76 0.463
448
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 68 0.463
449
CHD001 Chediak-Higashi Syndrome 67 0.463
450
P HMN036 Hemangiopericytoma, Malignant 58 0.463
451
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 54 0.463
452
c WLM013 Wilms Tumor 1 66 0.463
453
c NPH055 Nephrotic Syndrome, Type 1 52 0.463
454
VTR016 Vater/vacterl Association 49 0.463
455
P SCL057 Scoliosis, Isolated 1 40 0.463
456
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 66 0.463
457
P STR020 Strabismus 56 0.463
458
P RNL100 Renal Hypodysplasia/aplasia 1 63 0.463
459
c ALT008 Alternating Hemiplegia of Childhood 1 39 0.463
460
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.463
461
MLD001 Melioidosis 67 0.463
462
CHL065 Cholangiocarcinoma 58 0.463
463
c NMN014 Niemann-Pick Disease, Type C2 49 0.463
464
STT041 Stuttering 52 0.463
465
CLR109 Colorectal Adenocarcinoma 50 0.463
466
OVR105 Ovarian Serous Carcinoma 37 0.463
467
GLC003 Glucose Intolerance 54 0.463
468
P PRS062 Persistent Hyperplastic Primary Vitreous 48 0.463
469
IMM174 Immunodeficiency with Hyper-Igm, Type 1 64 0.463
470
NPH003 Nephrocalcinosis 49 0.463
471
CRH001 Crohn's Disease 80 0.463
472
c CHR684 Chronic Kidney Disease 69 0.463
473
P HYP087 Hypotrichosis 42 0.463
474
AVN001 Avian Influenza 61 0.463
475
BRN018 Borna Disease 36 0.463
476
SPC005 Speech Disorder 45 0.463
477
P PSR002 Psoriasis 63 0.463
478
MCH006 Mechanical Strabismus 40 0.463
479
P DBT009 Diabetes Mellitus 67 0.463
480
47X002 47,xyy 48 0.463
481
DFF036 Differentiated Thyroid Carcinoma 51 0.463
482
CNT115 Central Nervous System Embryonal Tumor 21 0.463
483
HRT011 Heart Septal Defect 49 0.463
484
P PTT006 Pituitary Adenoma 55 0.463
485
PNC129 Pancreatic Adenocarcinoma 65 0.463
486
P LVR013 Liver Disease 69 0.463
487
SVR001 Severe Acute Respiratory Syndrome 67 0.463
488
PLM001 Pulmonary Tuberculosis 69 0.463
489
P OLG002 Oligodendroglioma 66 0.463
490
c HPT001 Hepatitis C 62 0.463
491
P FBR017 Fibrosarcoma 56 0.463
492
P PLM036 Pulmonary Fibrosis 66 0.463
493
P GST044 Gastritis 55 0.463
494
THL004 Theileriasis 31 0.463
495
P SYS005 Systemic Scleroderma 74 0.463
496
CLR017 Clear Cell Sarcoma 44 0.463
497
P EPT012 Epithelioid Sarcoma 41 0.463
498
FLL031 Follicular Adenoma 40 0.463
499
ADN018 Adenoma 59 0.463
500
MYF001 Myofibroma 42 0.463
501
PST011 Pustulosis of Palm and Sole 52 0.463
502
MLG079 Malignant Pleural Mesothelioma 42 0.463
503
OST012 Osteoarthritis 77 0.463
504
BNG036 Bone Giant Cell Tumor 49 0.463
505
c CNG023 Congenital Fibrosarcoma 41 0.463
506
HYP082 Hypopharynx Cancer 47 0.463
507
P DRM010 Dermatomyositis 61 0.463
508
c MCR113 Microvascular Complications of Diabetes 3 52 0.463
509
c MCR133 Microvascular Complications of Diabetes 4 41 0.463
510
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.463
511
c DFN382 Deafness, Autosomal Dominant 76 18 0.463
512
P HMP002 Hemophagocytic Lymphohistiocytosis 61 0.463
513
TCK001 Tick-Borne Encephalitis 59 0.463
514
P DNG005 Dengue Virus 56 0.463
515
c PRC016 Pre-Eclampsia 65 0.463
516
BRN028 Brain Cancer 74 0.463
517
CHG001 Chagas Disease 66 0.463
518
CRT013 Carotid Stenosis 51 0.463
519
MYP001 Myoepithelioma 37 0.463
520
END041 Endometrial Adenocarcinoma 64 0.463
521
P ATR010 Atrial Heart Septal Defect 58 0.463
522
P HPT021 Hepatitis 69 0.463
523
PRV003 Perivascular Epithelioid Cell Tumor 38 0.463
524
GST033 Gestational Diabetes 61 0.463
525
P CRD119 Cardiac Arrest 67 0.463
526
P RSP003 Respiratory Failure 74 0.463
527
MCR013 Microphthalmia 60 0.463
528
CYS010 Cystinosis 62 0.463
529
CNG034 Congestive Heart Failure 69 0.463
530
P PRN023 Prion Disease 60 0.463
531
THY020 Thyroid Hyalinizing Trabecular Adenoma 20 0.463
532
INT079 Intrahepatic Cholangiocarcinoma 51 0.463
533
P INT068 Intestinal Disease 53 0.463
534
P OVR046 Ovarian Cyst 46 0.463
535
PSD016 Pseudosarcomatous Fibromatosis 37 0.463
536
ANP009 Anaplastic Oligodendroglioma 41 0.463
537
SRS001 Serous Cystadenocarcinoma 52 0.463
538
LPD008 Lipid Metabolism Disorder 62 0.463
539
P THY023 Thymoma 64 0.463
540
MDD011 Mood Disorder 62 0.463
541
CHN004 Chondroblastoma 41 0.463
542
P BNG032 Benign Mesothelioma 53 0.463
543
DRM006 Dermatitis 62 0.463
544
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.463
545
NWC001 Newcastle Disease 47 0.463
546
LYS002 Lysosomal Storage Disease 51 0.463
547
DMY004 Demyelinating Disease 50 0.463
548
P SCL048 Sclerosteosis 58 0.463
549
PLM010 Pulmonary Edema 55 0.463
550
VCT001 Vacterl Association 47 0.463
551
CHL028 Childhood Type Dermatomyositis 59 0.463
552
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.463
553
CRB037 Cerebral Palsy 67 0.463
554
HST024 Hist1h1e Syndrome 11 0.463
555
FSC004 Fasciitis 49 0.463
556
PTH003 Pathologic Nystagmus 52 0.463
557
MYX011 Myxozoa 18 0.463
558
c PSD047 Pseudo-Turner Syndrome 52 0.463
559
WLL004 Wallerian Degeneration 38 0.463
561
P CRB088 Cerebral Atrophy 33 0.463
562
P MGL013 Megalencephaly 45 0.463
563
NRN016 Neuronal Migration Disorders 40 0.463
564
CYT002 Cytokine Deficiency 43 0.463
565
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.463
566
PCT001 Pectus Carinatum 33 0.463
567
CHR176 Chromophil Renal Cell Carcinoma 23 0.463
568
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 0.463
569
EXN003 Exencephaly 30 0.463
570
HMM003 Hemimegalencephaly 48 0.463
571
ALL014 Allergic Encephalomyelitis 34 0.463
572
DWR001 Dwarfism 44 0.463
573
FBR019 Fibromatosis 42 0.463
574
MSL001 Measles 61 0.463
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