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Search results for wnt1

449 hits were found for wnt1

# Family MCID Name MIFTS Score
1
c OST110 Osteogenesis Imperfecta, Type Xv 39 38.819
2
c BNM030 Bone Mineral Density Quantitative Trait Locus 16 19 31.448
3
BRT054 Brittle Bone Disorder 74 31.325
4
P OST002 Osteoporosis 76 29.761
5
P BRS047 Breast Cancer 98 25.859
6
c OST164 Osteoporosis, Juvenile 54 23.303
7
P CLR023 Colorectal Cancer 100 23.249
8
P GST053 Gastric Cancer 83 21.073
9
P HPT023 Hepatocellular Carcinoma 96 20.073
10
P OST122 Osteogenesis Imperfecta, Type Iii 57 19.739
11
P PRS040 Prostate Cancer 95 16.901
12
c OST121 Osteogenesis Imperfecta, Type Iv 49 15.174
13
P CRB045 Cerebellar Hypoplasia 40 14.609
14
CLF027 Cleft Palate, Isolated 64 13.825
15
P MDL005 Medulloblastoma 75 13.333
16
P PTS002 Ptosis 52 13.186
17
P DNT011 Dentinogenesis Imperfecta 52 12.509
18
c BSL007 Basal Cell Carcinoma 68 12.391
19
NRL016 Neural Tube Defects 81 10.117
20
OST024 Osteoporosis-Pseudoglioma Syndrome 60 9.153
21
P VNB005 Van Buchem Disease 58 9.073
22
DBL002 Double Outlet Right Ventricle 57 8.643
23
P PRS062 Persistent Hyperplastic Primary Vitreous 48 7.625
24
MYX005 Myxoid Liposarcoma 65 7.154
25
P ORF002 Orofacial Cleft 43 7.154
26
ODN023 Odontochondrodysplasia 67 7.154
27
DSS008 Disease of Mental Health 74 7.154
28
GST026 Gastric Fundus Cancer 32 7.154
29
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 6.278
30
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 6.278
31
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 5.157
32
SQM006 Squamous Cell Carcinoma 60 4.815
33
P LNG032 Lung Cancer 98 4.549
34
c SML038 Small Cell Cancer of the Lung 69 4.541
35
P BND020 Bone Disease 59 4.253
36
P HYD006 Hydrocephalus 61 3.619
37
P ART022 Arthritis 71 3.571
38
RNL077 Renal Fibrosis 46 3.490
39
THY029 Thyroid Carcinoma 51 3.332
40
P LNG064 Lung Cancer Susceptibility 3 70 3.332
41
CRV035 Cervical Cancer 73 3.280
42
OST159 Osteogenic Sarcoma 66 3.185
43
P NRB001 Neuroblastoma 66 3.185
44
P RHM011 Rheumatoid Arthritis 82 2.998
45
BNR002 Bone Resorption Disease 47 2.988
46
c MCR130 Microvascular Complications of Diabetes 6 41 2.958
47
c MCR120 Microvascular Complications of Diabetes 7 47 2.958
48
P PLM036 Pulmonary Fibrosis 66 2.958
49
c MCR113 Microvascular Complications of Diabetes 3 52 2.958
50
c MCR133 Microvascular Complications of Diabetes 4 41 2.958
51
LNT004 Lentigines 46 2.936
52
PLM134 Pulmonary Fibrosis, Idiopathic 76 2.779
53
SVR004 Severe Combined Immunodeficiency 72 2.772
54
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 2.714
55
ORL015 Oral Squamous Cell Carcinoma 43 2.714
56
P MYC007 Myocardial Infarction 70 2.693
57
c CHR684 Chronic Kidney Disease 69 2.654
58
P PNC035 Pancreatic Cancer 86 2.650
59
HLX001 Helix Syndrome 48 2.640
60
P ADN016 Adenocarcinoma 63 2.578
61
AML029 Ameloblastoma 47 2.529
62
END057 Endometrial Cancer 72 2.528
63
P SCL048 Sclerosteosis 58 2.471
64
CL1007 Col1a1/2 Osteogenesis Imperfecta 26 2.471
65
c WLM013 Wilms Tumor 1 66 2.461
66
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 2.461
67
c DWL002 Dowling-Degos Disease 1 58 2.411
68
P BCL017 B-Cell Lymphoma 59 2.411
69
P OVR042 Ovarian Cancer 88 2.401
70
P MLN008 Melanoma 76 2.392
71
P PHC003 Pheochromocytoma 69 2.319
72
ADR040 Adrenal Gland Pheochromocytoma 46 2.319
73
ATH013 Atherosclerosis Susceptibility 63 2.285
74
P CRN037 Craniosynostosis 68 2.285
75
UTR056 Uterine Corpus Endometrial Carcinoma 27 2.243
76
CRV038 Cervical Squamous Cell Carcinoma 58 2.218
77
URT010 Ureteral Obstruction 45 2.162
78
FTT001 Fatty Liver Disease 62 2.162
79
P BRS044 Breast Adenocarcinoma 58 2.162
80
SPN186 Spinal Cord Injury 61 2.149
81
ATM095 Autoimmune Disease 61 2.149
82
P INS002 in Situ Carcinoma 53 2.149
83
P HYP265 Hypotonia 42 2.149
84
DCT002 Ductal Carcinoma in Situ 58 2.076
85
P SCL018 Scoliosis 57 2.076
86
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 2.076
87
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 2.076
88
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 2.076
89
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 2.076
90
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 2.076
91
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 2.076
92
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 2.076
93
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 2.076
94
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 2.076
95
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 2.076
96
c CNG216 Congenital Hydrocephalus 53 2.076
97
P KRT007 Keratoconus 50 2.072
98
KRT063 Keratocystic Odontogenic Tumor 39 2.000
99
c ATS007 Autism Spectrum Disorder 72 2.000
100
OBS082 Obstructive Nephropathy 41 1.983
101
CNT061 Conotruncal Heart Malformations 66 1.942
102
GLL048 Glial Tumor 52 1.942
103
GLM045 Glioma 63 1.942
104
PRG071 Progressive Pseudorheumatoid Dysplasia 45 1.884
105
ISC004 Ischemia 61 1.884
106
ANX004 Anoxia 40 1.833
107
RNL114 Renal Cell Carcinoma, Nonpapillary 80 1.833
108
P CLD001 Cleidocranial Dysplasia 64 1.833
109
ESP021 Esophageal Cancer 83 1.833
110
ANG020 Angiosarcoma 64 1.833
111
CNS004 Constipation 56 1.833
112
P END044 Endometriosis 62 1.833
113
c CLD019 Cleidocranial Dysplasia Spectrum Disorder 20 1.833
114
P PRR016 Pierre Robin Syndrome 50 1.762
115
ISL075 Isolated Pierre Robin Sequence 29 1.762
116
c ATR087 Atrial Standstill 1 74 1.740
117
CLR030 Clear Cell Renal Cell Carcinoma 54 1.740
118
LNG099 Lung Disease 62 1.740
119
PLC002 Plica Syndrome 35 1.740
120
SYN007 Synovitis 55 1.740
121
CYT002 Cytokine Deficiency 43 1.740
122
P FML011 Familial Adenomatous Polyposis 71 1.698
123
AGN016 Aging 54 1.640
124
c AMY091 Amyotrophic Lateral Sclerosis 1 88 1.640
125
c MCR115 Microvascular Complications of Diabetes 5 65 1.640
126
MYL005 Myelofibrosis 71 1.640
127
P STR020 Strabismus 56 1.640
128
c HYP521 Hypogonadotropic Hypogonadism 10 with or Without Anosmia 26 1.640
129
MCH006 Mechanical Strabismus 40 1.640
130
SYS071 Systemic Autoimmune Disease 35 1.640
131
CRT017 Cartilage Disease 53 1.640
132
P LTR001 Lateral Sclerosis 58 1.640
133
HYP266 Hypoxia 57 1.640
134
PRT251 Proteinuria, Chronic Benign 57 1.562
135
CLF001 Cleft Lip 53 1.562
136
c PRC016 Pre-Eclampsia 65 1.562
137
P VSC007 Vascular Disease 63 1.562
138
FRN006 Frontotemporal Dementia 68 1.529
139
P SPP010 Suppressor of Tumorigenicity 3 51 1.529
140
P DBT009 Diabetes Mellitus 67 1.529
141
P FBR017 Fibrosarcoma 56 1.529
142
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.529
143
ALT003 Alternating Exotropia 33 1.529
144
EXT022 Exotropia 42 1.529
145
c CNG513 Congenital Ptosis 42 1.529
146
c TYP009 Type 2 Diabetes Mellitus 92 1.496
147
ALL029 Allergic Disease 59 1.496
148
CLF004 Cleft Lip/palate 57 1.489
149
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.489
150
PLM014 Pleomorphic Adenoma 51 1.489
151
ATS010 Autosomal Recessive Disease 42 1.413
152
GLB002 Glioblastoma 67 1.413
153
OST012 Osteoarthritis 77 1.413
154
DPH001 Diphtheria 59 1.413
155
P HNT016 Huntington Disease 73 1.403
156
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.403
157
P MSC003 Muscular Atrophy 52 1.403
158
INT007 Intermediate Coronary Syndrome 54 1.403
159
EXP004 Exophthalmos 51 1.403
160
c HYP546 Hypogonadotropic Hypogonadism 20 with or Without Anosmia 24 1.403
161
P PLY006 Polydactyly 59 1.332
162
P MCR010 Microcephaly 60 1.332
163
48X005 48,xyyy 39 1.332
164
c TYP008 Type 1 Diabetes Mellitus 70 1.253
165
TLN003 Telangiectasis 51 1.253
166
LRY018 Laryngeal Squamous Cell Carcinoma 44 1.253
167
CLT003 Colitis 63 1.246
168
P JBR020 Joubert Syndrome 1 74 1.246
169
BRN004 Brain Edema 54 1.246
170
ULC004 Ulcerative Colitis 74 1.246
171
P VNT002 Ventricular Septal Defect 58 1.246
172
MCR013 Microphthalmia 60 1.246
173
c SCL052 Scleroderma, Familial Progressive 61 1.154
174
CHR103 Charge Syndrome 66 1.154
175
P ART023 Arthropathy 61 1.154
176
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.154
177
c SVR005 Severe Pre-Eclampsia 50 1.154
178
BRN071 Brain Injury 50 1.154
179
ART140 Arteries, Anomalies of 53 1.058
180
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 1.058
181
BRN003 Branchiooculofacial Syndrome 53 1.058
182
P ATX030 Ataxia-Telangiectasia 80 1.058
183
LPP008 Lipoprotein Quantitative Trait Locus 65 1.058
184
c HYP836 Hypercholesterolemia, Familial, 1 73 1.058
185
P KDN018 Kidney Disease 72 1.058
186
IGG001 Iga Glomerulonephritis 50 1.058
187
INS001 Insulinoma 59 1.058
188
P OVR082 Overgrowth Syndrome 49 1.053
189
P ALG028 Alagille Syndrome 1 73 1.053
190
CLB010 Coloboma of Macula 53 1.053
191
P SLV026 Salivary Gland Carcinoma 58 1.053
192
END086 End Stage Renal Disease 52 1.053
193
CRB004 Cerebral Artery Occlusion 45 1.053
194
P ENC008 Encephalocele 46 1.053
195
EXN003 Exencephaly 30 1.053
196
OVR094 Ovarian Epithelial Cancer 39 1.053
197
P ALZ034 Alzheimer Disease 87 0.942
198
P NSP012 Nasopharyngeal Carcinoma 61 0.942
199
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.942
200
P RTN024 Retinoblastoma 73 0.942
201
c EXS019 Exostoses, Multiple, Type I 54 0.942
202
c ACT075 Acute Myocardial Infarction 56 0.942
203
ORF053 Orofacial Clefting Syndrome 31 0.942
204
HRT011 Heart Septal Defect 49 0.942
205
P GST044 Gastritis 55 0.942
206
RCK004 Rickets 68 0.942
207
P FCL005 Focal Segmental Glomerulosclerosis 57 0.942
208
CHL014 Cholera 62 0.942
209
c HPT016 Hepatitis B 62 0.942
210
SKL017 Skeletal Dysplasias 41 0.816
211
c JVN041 Juvenile Nephronophthisis 43 0.816
212
c ORF037 Orofaciodigital Syndrome I 59 0.816
213
PRS129 Prostatic Hyperplasia, Benign 49 0.816
214
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.816
215
PLY150 Polykaryocytosis Inducer 29 0.816
216
BRK010 Burkitt Lymphoma 66 0.816
217
P PRK057 Parkinson Disease, Late-Onset 80 0.816
218
ARM010 Arima Syndrome 56 0.816
219
c LKM063 Leukemia, Chronic Myeloid 71 0.816
220
c JBR004 Joubert Syndrome 2 48 0.816
221
c BRN108 Branchiootic Syndrome 1 62 0.816
222
c JBR013 Joubert Syndrome 8 44 0.816
223
ULN003 Ulnar-Mammary Syndrome 56 0.816
224
P SNR003 Senior-Loken Syndrome 1 58 0.816
225
P HRS035 Hirschsprung Disease 1 66 0.816
226
CHL065 Cholangiocarcinoma 58 0.816
227
P BRC015 Bruck Syndrome 48 0.816
228
P MYL006 Myeloid Leukemia 61 0.816
229
OCC011 Occipital Encephalocele 26 0.816
230
HYP066 Hyperglycemia 61 0.816
231
MLG079 Malignant Pleural Mesothelioma 42 0.816
232
c DLT002 Dilated Cardiomyopathy 78 0.816
233
P ESP024 Esophagitis 60 0.816
234
PRS021 Prostatic Adenoma 43 0.816
235
P NPH005 Nephronophthisis 56 0.816
236
P RSP003 Respiratory Failure 74 0.816
237
PRS045 Prostatic Hypertrophy 53 0.816
238
INT079 Intrahepatic Cholangiocarcinoma 51 0.816
239
P RTN018 Retinal Disease 53 0.816
240
P TCD001 Tic Disorder 49 0.816
241
P BNG032 Benign Mesothelioma 53 0.816
242
ANK001 Ankylosis 51 0.816
243
c JVN010 Juvenile Rheumatoid Arthritis 66 0.816
244
MD2001 Med23 20 0.816
245
ISL109 Isolated Cleft Lip 33 0.666
246
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.666
247
c BNM016 Bone Mineral Density Quantitative Trait Locus 1 24 0.666
248
ANX010 Anxiety 70 0.666
249
c PLM164 Pulmonary Hypertension, Primary, 1 76 0.666
250
P FRN036 Frontonasal Dysplasia 1 44 0.666
251
P PLM037 Pulmonary Hypertension 72 0.666
252
HYP017 Hypophosphatemia 49 0.666
253
FML037 Female Breast Cancer 51 0.666
254
FTL006 Fetal Alcohol Spectrum Disorder 43 0.666
255
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 60 0.666
256
P ATR011 Atrial Fibrillation 66 0.666
257
P ANT088 Anterior Segment Dysgenesis 55 0.666
258
P BRC006 Brachydactyly 51 0.666
259
P SML001 Small Cell Carcinoma 52 0.666
260
RHM028 Rheumatic Heart Disease 56 0.666
261
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.666
262
SPN405 Spondyloepiphyseal Dysplasia Tarda, X-Linked 47 0.666
263
P CHN012 Chondrosarcoma 57 0.666
264
P CRN013 Craniodiaphyseal Dysplasia 43 0.666
265
FNC009 Fanconi-Bickel Syndrome 53 0.666
266
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.666
267
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 0.666
268
P CXV002 Coxa Vara 33 0.666
269
SPN209 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations 66 0.666
270
CRN220 Craniodiaphyseal Dysplasia, Autosomal Dominant 27 0.666
271
P GLM040 Glioma Susceptibility 1 71 0.666
272
VLP002 Valproate Embryopathy 38 0.666
273
MNN043 Meningioma, Familial 79 0.666
274
P PTN014 Patent Ductus Arteriosus 1 59 0.666
275
TNG007 Tongue Carcinoma 52 0.666
276
P HLP001 Holoprosencephaly 69 0.666
277
DGN001 Degenerative Disc Disease 49 0.666
278
P PLM034 Pulmonary Emphysema 58 0.666
279
P PTT006 Pituitary Adenoma 55 0.666
280
TRT001 Teratocarcinoma 42 0.666
281
PRT036 Peritonitis 65 0.666
282
SCR001 Secretory Meningioma 40 0.666
283
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.666
284
P LKM002 Leukemia 67 0.666
285
END041 Endometrial Adenocarcinoma 64 0.666
286
P ATR010 Atrial Heart Septal Defect 58 0.666
287
CRN027 Corneal Neovascularization 47 0.666
288
P HPT021 Hepatitis 69 0.666
289
MLG169 Malignant Astrocytoma 57 0.666
290
P HRT032 Heart Disease 81 0.666
291
GST033 Gestational Diabetes 61 0.666
292
P PLY011 Polycystic Ovary Syndrome 57 0.666
293
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.666
294
PNC002 Pancreatic Mucinous Cystadenoma 31 0.666
295
OBS004 Obstructive Hydrocephalus 45 0.666
296
PPT001 Peptic Esophagitis 52 0.666
297
SPN021 Spinal Meningioma 50 0.666
298
HYP572 Hypoganglionosis 27 0.666
299
c LKM005 Leukemia, T-Cell, Chronic 34 0.666
300
DPR016 Depression 65 0.666
301
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.666
302
P OST028 Osteochondroma 45 0.666
303
DWR001 Dwarfism 44 0.666
304
P AST005 Asthma 76 0.587
305
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 0.587
306
ADN011 Adenoid Cystic Carcinoma 68 0.517
307
CNG284 Congenital Pseudoarthrosis of the Tibia 17 0.471
308
WLL022 Well-Differentiated Fetal Adenocarcinoma of the Lung 16 0.471
309
MLF009 Malformation of the Cerebellar Vermis 5 0.471
310
INT358 Intestinal Polyposis Syndrome 25 0.471
311
P PLY187 Polyarticular Juvenile Idiopathic Arthritis 39 0.471
312
c ACT134 Acute Liver Failure 59 0.471
313
P BLD134 Bladder Cancer 79 0.471
314
SPP011 Suppression of Tumorigenicity 12 61 0.471
315
SMT008 Smith-Magenis Syndrome 54 0.471
316
P WSK001 Wiskott-Aldrich Syndrome 72 0.471
317
P FRG001 Fragile X Syndrome 70 0.471
318
CRD132 Cardiac Conduction Defect 60 0.471
319
ACR008 Acrocallosal Syndrome 70 0.471
320
P MYC084 Mycobacterium Tuberculosis 1 68 0.471
321
P SCH015 Schizophrenia 74 0.471
322
CLF028 Cleft Soft Palate 38 0.471
323
ALC007 Alcohol Dependence 66 0.471
324
c SPN225 Spondyloarthropathy 1 70 0.471
325
WLL001 Williams-Beuren Syndrome 61 0.471
326
ANS023 Anus, Imperforate 56 0.471
327
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 61 0.471
328
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 63 0.471
329
P CRN038 Carney Complex Variant 64 0.471
330
P APL001 Aplastic Anemia 73 0.471
331
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 0.471
332
HYP457 Hypertrophic Scars 42 0.471
333
P LYS001 Loeys-Dietz Syndrome 65 0.471
334
c PRK052 Parkinson Disease 17 43 0.471
335
TTH002 Tooth Agenesis 61 0.471
336
DFF005 Diffuse Large B-Cell Lymphoma 54 0.471
337
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.471
339
ACT098 Acute Erythroid Leukemia 55 0.471
340
NNL006 Non-Alcoholic Steatohepatitis 54 0.471
341
LWG006 Low Grade Glioma 41 0.471
342
P LYM033 Lymphoproliferative Syndrome 59 0.471
343
MYL020 Myelomeningocele 51 0.471
344
P LYM118 Lymphoma 67 0.471
345
c ATM022 Autoimmune Myocarditis 36 0.471
346
HLC007 Helicobacter Pylori Infection 67 0.471
347
END020 Endocardial Fibroelastosis 51 0.471
348
c TRC091 Trichorhinophalangeal Syndrome, Type Ii 51 0.471
349
P PRD006 Prader-Willi Syndrome 61 0.471
350
P LKM062 Leukemia, Acute Lymphoblastic 69 0.471
351
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.471
352
VRH001 Verheij Syndrome 39 0.471
353
c PCH010 Pachyonychia Congenita 3 43 0.471
354
c HPT073 Hepatitis C Virus 71 0.471
355
c OST132 Osteogenesis Imperfecta, Type Vi 45 0.471
356
c SCL042 Sclerosteosis 2 40 0.471
357
P ESP035 Esophagitis, Eosinophilic, 1 58 0.471
358
P DVL012 Developmental Dysplasia of the Hip 1 46 0.471
359
TBL029 Tubulin, Beta 28 0.471
360
MND020 Mandibulofacial Dysostosis, Guion-Almeida Type 51 0.471
361
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.471
362
P ACT092 Acth-Independent Macronodular Adrenal Hyperplasia 56 0.471
363
CHR619 Chromosome 2q35 Duplication Syndrome 64 0.471
364
c TRC092 Trichorhinophalangeal Syndrome, Type I 54 0.471
365
c TBR025 Tuberous Sclerosis 1 84 0.471
366
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.471
367
PPL048 Papillorenal Syndrome 58 0.471
368
ERM002 Ear Malformation 36 0.471
369
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.471
370
c NRF024 Neurofibromatosis, Type I 72 0.471
371
P RBN002 Robinow Syndrome 51 0.471
372
P SYN057 Syndromic Intellectual Disability 38 0.471
373
P NNS031 Non-Syndromic Intellectual Disability 32 0.471
374
OST017 Osteomyelitis 63 0.471
375
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 55 0.471
376
P HRD008 Hereditary Hemorrhagic Telangiectasia 65 0.471
377
P MTP001 Metaphyseal Dysplasia 38 0.471
378
P MYP006 Myopia 56 0.471
379
FCL090 Facial Cleft 30 0.471
380
RPD005 Rapidly Involuting Congenital Hemangioma 46 0.471
381
CRH001 Crohn's Disease 80 0.471
382
P RHB003 Rhabdomyosarcoma 66 0.471
383
P RBL001 Rubella 58 0.471
384
P HRP006 Herpes Simplex 65 0.471
385
DBT010 Diabetic Neuropathy 54 0.471
386
P ALP008 Alopecia 54 0.471
387
P HYP098 Hypereosinophilic Syndrome 66 0.471
388
SKN016 Skin Disease 63 0.471
389
P LVR013 Liver Disease 69 0.471
390
c HPT001 Hepatitis C 62 0.471
391
DYS018 Dysostosis 44 0.471
392
MTS001 Mutism 44 0.471
393
LNG039 Lung Squamous Cell Carcinoma 57 0.471
394
SPN035 Spindle Cell Sarcoma 54 0.471
395
CNN005 Connective Tissue Disease 67 0.471
396
P INF038 Influenza 68 0.471
397
P ORF001 Orofaciodigital Syndrome 50 0.471
398
SPN051 Spondylitis 51 0.471
399
INT071 Intestinal Perforation 49 0.471
401
c HYP532 Hypogonadotropic Hypogonadism 18 with or Without Anosmia 27 0.471
402
P SNS001 Sensorineural Hearing Loss 59 0.471
403
P DNG005 Dengue Virus 56 0.471
404
P DMN002 Dementia 66 0.471
405
P MLN007 Male Infertility 56 0.471
406
INF009 Inflammatory Spondylopathy 30 0.471
407
P HYP086 Hypothyroidism 69 0.471
408
CLN015 Colon Adenocarcinoma 65 0.471
409
TST014 Testicular Cancer 52 0.471
410
HGH043 High Grade Glioma 45 0.471
411
P TBR001 Tuberous Sclerosis 69 0.471
412
P ECL001 Eclampsia 52 0.471
413
IDP011 Idiopathic Interstitial Pneumonia 59 0.471
414
SRC014 Sarcoma 65 0.471
415
INT030 Intracranial Aneurysm 55 0.471
416
PRM013 Premature Menopause 58 0.471
417
BLL004 Bullous Keratopathy 48 0.471
418
c INF023 Inflammatory Breast Carcinoma 49 0.471
419
P INF032 Infertility 57 0.471
420
P PRP019 Peripheral Nervous System Disease 58 0.471
421
P TRT010 Teratoma 51 0.471
422
EMB004 Embryonal Carcinoma 56 0.471
423
c ACT071 Acute Kidney Failure 60 0.471
424
INT066 Interstitial Lung Disease 60 0.471
425
P MLT074 Multiple Endocrine Neoplasia 59 0.471
426
P KDN017 Kidney Cancer 61 0.471
427
CRB027 Cerebellar Disease 47 0.471
428
P MTR014 Motor Neuron Disease 65 0.471
429
DMY004 Demyelinating Disease 50 0.471
430
GST037 Gastroparesis 52 0.471
431
P GND004 Gonadal Dysgenesis 47 0.471
432
P OST001 Osteopetrosis 71 0.471
433
P ART005 Arteriovenous Malformation 65 0.471
434
MGC001 Megacolon 48 0.471
435
KRT008 Keratopathy 46 0.471
436
KLD004 Keloid Disorder 39 0.471
438
7Q1002 7q11.23 Duplication Syndrome 33 0.471
439
P NRF002 Neurofibromatosis 57 0.471
440
P MYC008 Myocarditis 59 0.471
441
P HYP055 Hypoplastic Left Heart Syndrome 65 0.471
442
DRG003 Drug Dependence 46 0.471
443
MTR027 Mitral Atresia 19 0.471
444
ORL011 Oral Cancer 60 0.471
445
c ERL012 Early-Onset Glaucoma 24 0.471
446
PTT037 Pituitary Tumors 44 0.471
447
ART030 Aortic Arch Interruption 25 0.471
448
CRB053 Cerebellar Agenesis 16 0.471
449
P NRV007 Nervous System Disease 67 0.471
The MalaCards human disease database index: 1-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
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