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Search results for heparan sulfate

523 hits were found for heparan sulfate

# Family MCID Name MIFTS Score
1
c MCP043 Mucopolysaccharidosis, Type Iiia 61 7.444
2
c MCP001 Mucopolysaccharidosis Iii 65 3.542
3
CNG363 Congenital Enterocyte Heparan Sulfate Deficiency 10 3.334
4
c EXS019 Exostoses, Multiple, Type I 53 0.322
5
CLT003 Colitis 62 0.321
6
P HRP006 Herpes Simplex 65 0.282
7
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.268
8
OST012 Osteoarthritis 78 0.238
9
c EXS020 Exostoses, Multiple, Type Ii 40 0.237
10
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.232
11
c PRC016 Pre-Eclampsia 63 0.227
12
P LYM118 Lymphoma 68 0.220
13
HMN044 Human Immunodeficiency Virus Type 1 71 0.209
14
48X005 48,xyyy 39 0.209
15
P ECL001 Eclampsia 50 0.200
16
P INF037 Inflammatory Bowel Disease 54 0.198
17
P LKM002 Leukemia 68 0.190
18
P BRS047 Breast Cancer 97 0.187
19
P HRD001 Hereditary Multiple Exostoses 46 0.186
20
c HRD104 Hereditary Multiple Osteochondromas 39 0.184
21
c MCR120 Microvascular Complications of Diabetes 7 47 0.179
22
c MCR113 Microvascular Complications of Diabetes 3 52 0.179
23
c MCR130 Microvascular Complications of Diabetes 6 41 0.179
24
c MCR133 Microvascular Complications of Diabetes 4 41 0.179
25
P NRB001 Neuroblastoma 72 0.177
26
c SYS001 Systemic Lupus Erythematosus 86 0.175
27
P AMY004 Amyloidosis 70 0.175
28
MCP033 Mucopolysaccharidoses 38 0.169
29
P CLR023 Colorectal Cancer 99 0.166
30
P ALZ034 Alzheimer Disease 88 0.163
31
P GLM007 Glomerulonephritis 57 0.159
32
P KDN018 Kidney Disease 72 0.155
33
P ADN016 Adenocarcinoma 64 0.155
34
P MLN008 Melanoma 69 0.154
35
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.153
36
P LKM062 Leukemia, Acute Lymphoblastic 69 0.149
37
IMM167 Immune Deficiency Disease 78 0.149
38
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.147
39
ATH013 Atherosclerosis Susceptibility 65 0.145
40
P VSC007 Vascular Disease 63 0.145
41
ACQ007 Acquired Immunodeficiency Syndrome 60 0.143
42
P DNG005 Dengue Virus 59 0.143
43
CYT002 Cytokine Deficiency 42 0.142
44
P GLM045 Glioma 63 0.141
45
GLB015 Glioblastoma Multiforme 75 0.141
46
MST004 Mast Cell Neoplasm 42 0.140
47
EXT007 Extracutaneous Mastocytoma 38 0.140
48
P FBR017 Fibrosarcoma 56 0.139
49
GLL048 Glial Tumor 45 0.139
50
P CHN012 Chondrosarcoma 56 0.136
51
P BCL017 B-Cell Lymphoma 58 0.134
52
P OVR042 Ovarian Cancer 88 0.134
53
KPS004 Kaposi Sarcoma 75 0.132
54
c MCP050 Mucopolysaccharidosis, Type Ii 72 0.127
55
P NPH012 Nephrotic Syndrome 60 0.126
56
ATM095 Autoimmune Disease 62 0.124
57
P ENC004 Encephalitis 61 0.124
58
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.123
59
NPH009 Nephrolithiasis 55 0.121
60
P DRR001 Diarrhea 55 0.121
61
SRC014 Sarcoma 65 0.117
62
SPN035 Spindle Cell Sarcoma 53 0.117
63
SPN186 Spinal Cord Injury 60 0.116
64
HLX001 Helix Syndrome 47 0.115
65
P LPS004 Lupus Erythematosus 61 0.115
66
P PRN023 Prion Disease 57 0.114
67
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.114
68
MTH009 Mouth Disease 56 0.113
69
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.113
70
c MCP045 Mucopolysaccharidosis, Type Iiic 59 0.112
71
CHL123 Chlamydia 59 0.112
72
VCC001 Vaccinia 49 0.111
73
HYP266 Hypoxia 57 0.111
74
HYP066 Hyperglycemia 61 0.111
75
ADN018 Adenoma 59 0.111
76
P PHC003 Pheochromocytoma 71 0.110
77
ADR040 Adrenal Gland Pheochromocytoma 46 0.110
78
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.108
79
c LKM005 Leukemia, T-Cell, Chronic 34 0.108
80
P HPT023 Hepatocellular Carcinoma 100 0.107
81
ALL026 Allergic Hypersensitivity Disease 62 0.107
82
HRL003 Hurler Syndrome 65 0.106
83
P CYS018 Cystitis 59 0.106
84
P LVR013 Liver Disease 68 0.105
85
P PNC035 Pancreatic Cancer 84 0.105
86
P HMN032 Human Herpesvirus 8 47 0.105
87
MYL069 Myeloma, Multiple 85 0.104
88
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.104
89
BNR002 Bone Resorption Disease 48 0.104
90
c HYP595 Hypertension, Essential 84 0.104
91
SCH036 Scheie Syndrome 72 0.104
92
SCR011 Scrapie 39 0.103
93
c SVR001 Severe Acute Respiratory Syndrome 62 0.103
94
c THR092 Thrombophilia Due to Thrombin Defect 73 0.103
95
BRK010 Burkitt Lymphoma 67 0.103
96
P OVR082 Overgrowth Syndrome 50 0.103
97
CHL068 Cholestasis 61 0.103
98
P SRC025 Sarcoidosis 1 70 0.102
99
P MMB011 Membranous Nephropathy 50 0.102
100
47X002 47,xyy 49 0.101
101
P CHR345 Chronic Pain 44 0.101
102
STM007 Stomatitis 50 0.101
103
P INT143 Interstitial Cystitis 61 0.099
104
P NRP001 Neuropathy 56 0.099
105
c HPT073 Hepatitis C Virus 72 0.098
106
P PLM036 Pulmonary Fibrosis 65 0.096
107
P HYP086 Hypothyroidism 69 0.096
108
P ATS364 Autism 70 0.095
109
P ENC018 Encephalopathy 61 0.095
110
P OST028 Osteochondroma 45 0.095
111
ARG004 Argyria 27 0.095
112
LYS002 Lysosomal Storage Disease 52 0.094
113
EXS001 Exostosis 46 0.094
114
END086 End Stage Renal Disease 51 0.094
115
LNG099 Lung Disease 60 0.092
116
HND002 Hand, Foot and Mouth Disease 51 0.091
117
P HYP750 Hypertriglyceridemia, Familial 62 0.089
118
c MLG068 Malignant Glioma 46 0.089
119
CHL014 Cholera 59 0.088
120
CRB039 Cerebrovascular Disease 67 0.088
121
JPN002 Japanese Encephalitis 57 0.088
122
EMB004 Embryonal Carcinoma 56 0.088
123
OST159 Osteogenic Sarcoma 66 0.087
124
SVR004 Severe Combined Immunodeficiency 73 0.087
125
c DBT099 Diabetes Mellitus, Type I 65 0.087
126
c HPT001 Hepatitis C 62 0.087
127
P LNG032 Lung Cancer 98 0.086
128
MLR004 Malaria 81 0.086
129
INS024 Insulin-Like Growth Factor I 79 0.086
130
P RHB003 Rhabdomyosarcoma 63 0.086
131
DWR001 Dwarfism 44 0.086
132
P MDL005 Medulloblastoma 77 0.086
133
ALL014 Allergic Encephalomyelitis 38 0.086
134
c MCP044 Mucopolysaccharidosis, Type Iiib 59 0.085
135
c AMY009 Amyloidosis Aa 50 0.085
136
P NRF002 Neurofibromatosis 56 0.085
137
P PLM037 Pulmonary Hypertension 67 0.084
138
LVR012 Liver Cirrhosis 62 0.084
139
P PRS040 Prostate Cancer 97 0.084
140
P BLD134 Bladder Cancer 79 0.084
141
c MCP046 Mucopolysaccharidosis, Type Iiid 51 0.083
142
P RTN024 Retinoblastoma 73 0.082
143
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.082
144
c FML008 Familial Retinoblastoma 53 0.082
145
CYT008 Cytomegalovirus Infection 57 0.082
146
PRP027 Peripheral Vascular Disease 71 0.081
147
P ART022 Arthritis 69 0.081
148
P KLL001 Kallmann Syndrome 61 0.081
149
TXC005 Toxic Shock Syndrome 62 0.081
150
P PRP019 Peripheral Nervous System Disease 58 0.080
151
P ADL017 Adult T-Cell Leukemia 56 0.080
152
P SYS005 Systemic Scleroderma 68 0.080
154
CRV035 Cervical Cancer 76 0.080
155
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.080
156
PRT037 Pertussis 65 0.080
157
CYS001 Cystic Fibrosis 81 0.079
158
P GST044 Gastritis 56 0.079
159
P MCR115 Microvascular Complications of Diabetes 5 66 0.078
160
SKN016 Skin Disease 63 0.078
161
c ACT027 Acute Pancreatitis 60 0.078
162
P LNG064 Lung Cancer Susceptibility 3 78 0.078
163
c MCP049 Mucopolysaccharidosis, Type Vii 63 0.077
164
P PRD008 Periodontitis 64 0.077
165
BRN028 Brain Cancer 74 0.076
166
LSH001 Leishmaniasis 63 0.076
167
P KLZ004 Kala-Azar 1 41 0.076
168
P RHM011 Rheumatoid Arthritis 80 0.075
169
CLN015 Colon Adenocarcinoma 65 0.075
170
P DBT009 Diabetes Mellitus 64 0.075
171
GST045 Gastroenteritis 59 0.075
172
IGG001 Iga Glomerulonephritis 48 0.075
173
PLY150 Polykaryocytosis Inducer 31 0.075
174
BRN024 Bronchitis 68 0.074
175
c NRF024 Neurofibromatosis, Type I 77 0.074
176
P EHL001 Ehlers-Danlos Syndrome 58 0.074
177
P EXN002 Exanthem 57 0.074
178
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.074
179
MCS002 Mucositis 56 0.073
180
P GRF003 Graft-Versus-Host Disease 72 0.073
181
c WLM013 Wilms Tumor 1 65 0.073
182
c HPT003 Hepatitis a 62 0.073
183
SYN007 Synovitis 54 0.073
184
NTR046 Neutrophil Migration 50 0.073
185
PLC002 Plica Syndrome 36 0.073
186
ALL006 Allergic Asthma 56 0.073
187
BCT022 Bacterial Infectious Disease 56 0.072
188
PRT019 Protein-Losing Enteropathy 45 0.072
189
c HPT016 Hepatitis B 59 0.072
190
CHR074 Choriocarcinoma 47 0.072
191
CHC001 Chickenpox 60 0.071
192
c DNG003 Dengue Disease 59 0.071
193
HRL004 Hurler-Scheie Syndrome 55 0.071
194
P PNC044 Pancreatitis 61 0.070
195
SQM006 Squamous Cell Carcinoma 60 0.070
196
RNL077 Renal Fibrosis 47 0.070
197
TTN003 Tetanus 65 0.070
198
DNG002 Dengue Hemorrhagic Fever 60 0.069
199
CHK001 Chikungunya 57 0.069
200
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.069
201
RCK004 Rickets 68 0.069
202
LPP008 Lipoprotein Quantitative Trait Locus 62 0.069
203
P HMR005 Hemorrhoid 46 0.069
204
LPD008 Lipid Metabolism Disorder 62 0.069
205
P PLY019 Polyneuropathy 56 0.069
206
P BNG032 Benign Mesothelioma 46 0.069
207
c LKM061 Leukemia, Acute Myeloid 84 0.068
208
P THR014 Thrombocytopenia 67 0.068
209
GST050 Gastrointestinal System Disease 56 0.068
210
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.067
211
EYD002 Eye Disease 58 0.067
212
ADN011 Adenoid Cystic Carcinoma 70 0.067
213
TRT001 Teratocarcinoma 45 0.067
214
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.066
215
END057 Endometrial Cancer 74 0.066
216
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.066
217
c WLM018 Wilms Tumor 5 61 0.066
218
URL001 Urolithiasis 45 0.066
220
P RTN016 Retinal Degeneration 53 0.066
221
P LTR001 Lateral Sclerosis 54 0.065
222
P INT068 Intestinal Disease 53 0.065
223
c DPH024 Diaphragmatic Hernia, Congenital 63 0.065
224
CHL065 Cholangiocarcinoma 68 0.064
225
INT079 Intrahepatic Cholangiocarcinoma 51 0.064
226
c HNT011 Huntington Disease-Like 3 38 0.064
227
SKN019 Skin Melanoma 68 0.064
228
P PSR002 Psoriasis 62 0.064
229
P CTR002 Cataract 60 0.064
230
PST011 Pustulosis of Palm and Sole 52 0.064
231
c SCL052 Scleroderma, Familial Progressive 61 0.063
232
P VNS003 Venous Insufficiency 55 0.063
233
P HPT021 Hepatitis 67 0.063
234
P MYL006 Myeloid Leukemia 60 0.063
235
P KDN017 Kidney Cancer 60 0.063
236
P BND020 Bone Disease 59 0.063
237
P SKN015 Skin Carcinoma 66 0.062
238
c MCR129 Microvascular Complications of Diabetes 1 66 0.062
239
HPR003 Heparin-Induced Thrombocytopenia 48 0.062
240
CRB004 Cerebral Artery Occlusion 45 0.062
242
MCR013 Microphthalmia 57 0.061
243
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.061
244
c MCP052 Mucopolysaccharidosis, Type Vi 67 0.061
245
P MSC005 Muscular Dystrophy 66 0.061
246
ART140 Arteries, Anomalies of 52 0.061
247
c ATS007 Autism Spectrum Disorder 67 0.061
248
KRT019 Keratitis, Hereditary 65 0.061
249
P VSC011 Vasculitis 62 0.061
250
RBS001 Rabies 58 0.061
251
HYP080 Hypogonadism 50 0.061
252
ATS010 Autosomal Recessive Disease 48 0.061
253
P OST002 Osteoporosis 74 0.060
254
P RNL100 Renal Hypodysplasia/aplasia 1 63 0.059
255
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.059
256
c CHR431 Chronic Venous Insufficiency 49 0.059
257
EST003 Eastern Equine Encephalitis 37 0.059
258
CRT072 Creutzfeldt-Jakob Disease 70 0.059
259
c DWL002 Dowling-Degos Disease 1 58 0.059
260
SPL018 Splenomegaly 48 0.059
261
PLM031 Poliomyelitis 64 0.058
262
P BRS044 Breast Adenocarcinoma 59 0.058
263
PPL022 Papilloma 54 0.058
264
SQM002 Squamous Cell Papilloma 46 0.058
265
BRS050 Breast Cyst 40 0.058
266
ESP021 Esophageal Cancer 90 0.057
267
CHG001 Chagas Disease 66 0.057
268
FTT001 Fatty Liver Disease 61 0.057
269
VRL011 Viral Infectious Disease 61 0.057
270
THY029 Thyroid Carcinoma 59 0.057
271
P SCK005 Sickle Cell Disease 50 0.057
272
SKL017 Skeletal Dysplasias 40 0.057
273
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.057
274
c PCH010 Pachyonychia Congenita 3 44 0.057
275
P HYP265 Hypotonia 43 0.057
276
MLT162 Multiple Joint Dislocations, Short Stature, and Craniofacial Dysmorphism with or Without Congenital Heart Defects 42 0.057
277
c MCR112 Microvascular Complications of Diabetes 2 41 0.057
278
IDP091 Idiopathic Nephrotic Syndrome 42 0.056
279
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.055
280
ATR057 Atrioventricular Block 55 0.055
281
INT002 Intermittent Claudication 61 0.054
282
YLL002 Yellow Fever 61 0.054
283
P EPD016 Epidermolysis Bullosa 53 0.054
284
HMC014 Homocysteinemia 53 0.054
285
P PRL003 Proliferative Glomerulonephritis 44 0.054
286
MDD018 Middle East Respiratory Syndrome 43 0.054
287
OVR094 Ovarian Epithelial Cancer 38 0.054
288
GLM044 Glomerular Disease 37 0.054
289
P PRK057 Parkinson Disease, Late-Onset 78 0.053
290
DPH001 Diphtheria 60 0.053
291
P SCL018 Scoliosis 60 0.053
292
PLM033 Pulmonary Embolism 59 0.053
293
P END039 Endodermal Sinus Tumor 44 0.053
294
TST018 Testicular Yolk Sac Tumor 39 0.053
295
P RTN008 Retinitis Pigmentosa 79 0.052
296
P MYC008 Myocarditis 59 0.052
297
TCK001 Tick-Borne Encephalitis 56 0.052
298
P MCL001 Mucolipidosis 48 0.052
299
PPL002 Papillary Carcinoma 47 0.052
300
DFF003 Diffuse Scleroderma 41 0.052
301
SPN331 Spondyloocular Syndrome 36 0.052
302
MSC157 Muscular Dystrophy, Duchenne Type 72 0.052
303
P NRV007 Nervous System Disease 66 0.052
304
P MLN069 Melanoma, Uveal 59 0.052
305
P SBS003 Substance Abuse 55 0.052
306
GLC003 Glucose Intolerance 54 0.052
307
KSH004 Kashin-Beck Disease 38 0.052
308
PNC129 Pancreatic Adenocarcinoma 68 0.050
309
P CLC063 Celiac Disease 1 66 0.050
310
ANR040 Aneurysm 59 0.050
311
THY122 Thyroid Gland Cancer 57 0.050
312
HYP017 Hypophosphatemia 50 0.050
313
NRL016 Neural Tube Defects 82 0.049
314
PCK003 Pick Disease of Brain 68 0.049
315
P HYP098 Hypereosinophilic Syndrome 67 0.049
316
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.049
317
CCC001 Coccidioidomycosis 58 0.049
318
CHR177 Chromophobe Renal Cell Carcinoma 57 0.049
319
P PLM034 Pulmonary Emphysema 55 0.049
320
RCS002 Recessive Dystrophic Epidermolysis Bullosa 54 0.049
321
P MNC007 Monocytic Leukemia 53 0.049
322
TRY001 Trypanosomiasis 50 0.049
323
RFT001 Rift Valley Fever 47 0.049
324
AML029 Ameloblastoma 46 0.049
325
LPD004 Lipoid Nephrosis 46 0.049
326
DNG001 Dengue Shock Syndrome 43 0.049
327
MCL022 Mucolipidoses 30 0.049
328
P CND004 Candidiasis 58 0.048
329
P UVT001 Uveitis 57 0.048
330
c MST023 Mesothelioma, Malignant 57 0.048
331
SCH014 Schistosomiasis 57 0.048
332
P GRV001 Graves' Disease 55 0.048
333
GNT003 Genital Herpes 54 0.048
334
GTR002 Goiter 53 0.048
335
P IGN003 Iga Nephropathy 1 49 0.048
336
URT010 Ureteral Obstruction 45 0.048
337
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.048
338
HML018 Homologous Wasting Disease 22 0.048
339
MRF001 Marfan Syndrome 77 0.046
340
P TRC072 Treacher Collins Syndrome 1 66 0.046
341
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.046
342
c LKM070 Leukemia, Acute Monocytic 57 0.046
343
OPT070 Optic Nerve Hypoplasia, Bilateral 56 0.046
344
FRY006 Fryns Microphthalmia Syndrome 52 0.046
345
CLB010 Coloboma of Macula 52 0.046
346
P HYP730 Hypogonadotropic Hypogonadism 52 0.046
347
ACT200 Acute Monoblastic Leukemia 52 0.046
348
CHL147 Chlamydia Pneumonia 48 0.046
349
CRN027 Corneal Neovascularization 47 0.046
350
CWP001 Cowpox 46 0.046
351
SZR028 Seizures, Scoliosis, and Macrocephaly/microcephaly Syndrome 37 0.046
352
P KNB001 Knobloch Syndrome 32 0.046
353
ISL004 Isolated Gonadotropin-Releasing Hormone Deficiency 26 0.046
354
IMM165 Immunoglobulin Switch Sequences 15 0.046
355
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.045
356
MYL005 Myelofibrosis 70 0.045
357
ART016 Aortic Aneurysm 69 0.045
358
c HMP004 Hemophilia B 68 0.045
359
CLF027 Cleft Palate, Isolated 64 0.045
360
P DRM010 Dermatomyositis 61 0.045
361
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.045
362
P GLL022 Guillain-Barre Syndrome 59 0.045
363
ERY051 Erythroleukemia, Familial 56 0.045
364
INT030 Intracranial Aneurysm 56 0.045
365
LMB062 Limb Ischemia 55 0.045
366
P RTN018 Retinal Disease 53 0.045
367
c VRL010 Viral Hepatitis 52 0.045
368
THY030 Thyroid Gland Disease 52 0.045
369
P HMP007 Hemophilia 51 0.045
370
CCN002 Cocaine Abuse 49 0.045
371
INT067 Interstitial Nephritis 48 0.045
372
c EHL076 Ehlers-Danlos Syndrome, Spondylodysplastic Type, 1 34 0.045
373
EXN003 Exencephaly 31 0.045
374
LYM017 Lyme Disease 64 0.043
375
c GLC092 Glaucoma, Primary Open Angle 62 0.043
376
GST033 Gestational Diabetes 61 0.043
377
INT066 Interstitial Lung Disease 60 0.043
378
P SYP003 Syphilis 58 0.043
379
BRN056 Bronchopulmonary Dysplasia 57 0.043
380
HMR039 Hemorrhage, Intracerebral 57 0.043
381
c CNT035 Central Nervous System Disease 52 0.043
382
c ACT135 Acute Graft Versus Host Disease 52 0.043
383
P SPP010 Suppressor of Tumorigenicity 3 51 0.043
384
P PST095 Post-Thrombotic Syndrome 51 0.043
385
P MYT002 Myotonic Dystrophy 49 0.043
386
P OPN001 Open-Angle Glaucoma 49 0.043
387
P CRV031 Cervical Adenocarcinoma 49 0.043
388
PRS063 Paresthesia 41 0.043
389
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.043
390
GDP001 Goodpasture Syndrome 55 0.041
391
SLP001 Sleeping Sickness 54 0.041
392
c FML015 Familial Nephrotic Syndrome 41 0.041
393
c RTN177 Retinitis Pigmentosa 73 35 0.041
394
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.040
395
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.040
396
c NMN015 Niemann-Pick Disease, Type C1 68 0.040
397
P MTR014 Motor Neuron Disease 65 0.040
398
CLR108 Colorectal Adenoma 64 0.040
399
NRL005 Neurilemmoma 60 0.040
400
P NMN002 Niemann-Pick Disease 59 0.040
401
P URF003 Urofacial Syndrome 1 57 0.040
402
EXF001 Exfoliation Syndrome 56 0.040
403
INT007 Intermediate Coronary Syndrome 55 0.040
404
WST005 West Nile Virus 54 0.040
405
P HMR003 Hemorrhagic Disease 53 0.040
406
P CNG436 Congenital Disorder of Deglycosylation 52 0.040
407
P THY032 Thyroiditis 52 0.040
408
GNG012 Gingival Overgrowth 51 0.040
409
c DSB006 Desbuquois Dysplasia 1 48 0.040
410
THY128 Thyroid Tumor 47 0.040
411
DYG001 Dyggve-Melchior-Clausen Disease 46 0.040
412
RTN023 Retinitis 46 0.040
413
RTN020 Retinal Vascular Disease 46 0.040
415
DYS018 Dysostosis 44 0.040
416
FBR054 Fibroma 44 0.040
417
NRR001 Neuroretinitis 42 0.040
418
MSN004 Mesenchymal Cell Neoplasm 41 0.040
419
P PSD087 Pseudoxanthoma Elasticum 65 0.037
420
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 64 0.037
421
P VNT002 Ventricular Septal Defect 60 0.037
422
HLC007 Helicobacter Pylori Infection 59 0.037
423
P PLY041 Polymyositis 57 0.037
424
VSC002 Vascular Dementia 57 0.037
425
c NPH055 Nephrotic Syndrome, Type 1 56 0.037
427
VGN023 Vaginitis 54 0.037
428
P HMC002 Homocystinuria 53 0.037
429
P RNL017 Renal Oncocytoma 53 0.037
430
IRD001 Iridocyclitis 53 0.037
431
c HPT007 Hepatitis E 53 0.037
432
DMY004 Demyelinating Disease 52 0.037
433
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 52 0.037
434
MCP006 Mucoepidermoid Carcinoma 50 0.037
435
HYP748 Hypertelorism 50 0.037
436
VLV047 Volvulus of Midgut 49 0.037
437
P CTN015 Cutaneous T Cell Lymphoma 49 0.037
438
VNZ002 Venezuelan Equine Encephalitis 47 0.037
439
CRS001 Crescentic Glomerulonephritis 43 0.037
440
c MCP051 Mucopolysaccharidosis, Type Ix 40 0.037
441
IMM001 Immune-Complex Glomerulonephritis 40 0.037
442
P DSB002 Desbuquois Dysplasia 32 0.037
443
P HRD084 Hereditary Cerebral Amyloid Angiopathy 32 0.037
444
ACT181 Acute Motor Axonal Neuropathy 26 0.037
445
LYS030 Lysosomal Storage Disease with Skeletal Involvement 25 0.037
446
P OST001 Osteopetrosis 70 0.032
447
c CNG411 Congenital Disorder of Glycosylation, Type in 68 0.032
448
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 68 0.032
450
DRM014 Dermatofibrosarcoma Protuberans 65 0.032
451
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.032
452
CNT061 Conotruncal Heart Malformations 63 0.032
453
ACT119 Acute Promyelocytic Leukemia 63 0.032
454
PTR032 Peters-Plus Syndrome 63 0.032
455
P ECT006 Ectodermal Dysplasia 62 0.032
456
P LRS001 Larsen Syndrome 62 0.032
457
P TRC086 Trichohepatoenteric Syndrome 1 62 0.032
458
BLL006 Bullous Pemphigoid 62 0.032
459
DCB001 Decubitus Ulcer 61 0.032
460
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.032
461
SPP011 Suppression of Tumorigenicity 12 59 0.032
462
WLF002 Wolf-Hirschhorn Syndrome 59 0.032
463
CSY001 C Syndrome 58 0.032
464
c ACT134 Acute Liver Failure 56 0.032
465
DBL002 Double Outlet Right Ventricle 56 0.032
466
SBC001 Subacute Sclerosing Panencephalitis 56 0.032
467
SML019 Smallpox 56 0.032
468
P WLL002 Weill-Marchesani Syndrome 56 0.032
469
CLR030 Clear Cell Renal Cell Carcinoma 53 0.032
470
P INS002 in Situ Carcinoma 53 0.032
471
OVR059 Ovary Adenocarcinoma 53 0.032
472
ONC002 Onchocerciasis 52 0.032
473
c NMN014 Niemann-Pick Disease, Type C2 51 0.032
474
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.032
475
ALK024 Alkuraya-Kucinskas Syndrome 51 0.032
476
THR016 Thrombophlebitis 51 0.032
477
P THR015 Thrombophilia 51 0.032
478
ASP003 Aseptic Meningitis 51 0.032
479
LNT004 Lentigines 50 0.032
480
RTN003 Retinal Ischemia 50 0.032
481
MYD002 Myd88 Deficiency 50 0.032
482
P SMP003 Simpson-Golabi-Behmel Syndrome 50 0.032
483
VLV011 Vulvovaginal Candidiasis 49 0.032
484
c HPT015 Hepatitis D 49 0.032
485
EBL001 Ebola Hemorrhagic Fever 49 0.032
486
ASB001 Asbestosis 47 0.032
487
HPT025 Hepatic Lipase Deficiency 47 0.032
488
HYD001 Hydranencephaly 44 0.032
489
P FRN036 Frontonasal Dysplasia 1 44 0.032
490
BCT021 Bacterial Sepsis 44 0.032
491
GRN007 Granuloma Annulare 44 0.032
492
CLN044 Colon Adenoma 44 0.032
493
P RPD001 Rapidly Progressive Glomerulonephritis 44 0.032
494
P HYP121 Hypoalphalipoproteinemia 43 0.032
495
VRL003 Variola Major 42 0.032
496
MNK002 Monkeypox 39 0.032
497
P CNG048 Congenital Hepatic Fibrosis 38 0.032
498
P OMD003 Omodysplasia 37 0.032
499
c CHR020 Chronic Interstitial Cystitis 37 0.032
500
c HYP548 Hypogonadotropic Hypogonadism 2 with or Without Anosmia 37 0.032
501
ANT002 Anti-Basement Membrane Glomerulonephritis 36 0.032
502
GST052 Gestational Choriocarcinoma 36 0.032
503
CRN022 Corneal Degeneration 36 0.032
504
PRN029 Parainfluenza Virus Type 3 36 0.032
505
c OMD001 Omodysplasia 1 35 0.032
506
SCL025 Scleromyxedema 32 0.032
507
CRN238 Corneal Dystrophy, Epithelial Basement Membrane 32 0.032
508
LRY004 Laryngotracheitis 31 0.032
509
MRR003 Murray Valley Encephalitis 29 0.032
510
c HYP511 Hypogonadotropic Hypogonadism 15 with or Without Anosmia 29 0.032
511
CNG506 Congenital Amyoplasia 27 0.032
512
ASB003 Asbestos Intoxication 26 0.032
513
c HYP817 Hypogonadotropic Hypogonadism 21 with or Without Anosmia 25 0.032
514
EPT025 Epithelial Basement Membrane Dystrophy 25 0.032
515
c JVN058 Juvenile-Onset Parkinson's Disease 25 0.032
516
c HYP546 Hypogonadotropic Hypogonadism 20 with or Without Anosmia 25 0.032
517
c HYP444 Hypogonadotropic Hypogonadism 9 with or Without Anosmia 24 0.032
518
CHR176 Chromophil Renal Cell Carcinoma 23 0.032
519
CHR247 Chromosome 4p Deletion 22 0.032
521
c EXS021 Exostoses, Multiple, Type Iii 20 0.032
522
MLN071 Melanoma Tumor Antigen Gp90 17 0.032
523
HND011 Hendra Virus Infection 12 0.032
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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