Search results for Chondroitin

517 hits were found for Chondroitin

# Family MCID Name MIFTS Score
1
BRC115 Brachyolmia Type 1, Toledo Type 14 4.145
2
OST012 Osteoarthritis 78 0.531
3
P CYS018 Cystitis 59 0.230
4
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.218
5
P INT143 Interstitial Cystitis 61 0.207
6
SPN186 Spinal Cord Injury 60 0.207
7
P CHN012 Chondrosarcoma 56 0.201
8
P MLN008 Melanoma 69 0.147
9
P ART023 Arthropathy 62 0.137
10
P ART022 Arthritis 69 0.130
11
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.130
12
P GLM045 Glioma 63 0.123
13
ATH013 Atherosclerosis Susceptibility 65 0.120
14
P NRB001 Neuroblastoma 72 0.116
15
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.116
16
SYN007 Synovitis 54 0.112
17
PLC002 Plica Syndrome 36 0.112
18
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.108
19
GLL048 Glial Tumor 45 0.108
20
GLB015 Glioblastoma Multiforme 75 0.104
21
c ACT068 Acute Cystitis 63 0.104
22
c PNS012 Paine Syndrome 61 0.104
23
MST004 Mast Cell Neoplasm 42 0.104
24
EXT007 Extracutaneous Mastocytoma 38 0.104
25
c CFF010 Coffin-Siris Syndrome 3 42 0.099
26
P PSR002 Psoriasis 62 0.095
27
PST011 Pustulosis of Palm and Sole 52 0.095
28
DGN001 Degenerative Disc Disease 48 0.095
29
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.095
30
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.090
31
LWC001 Low Compliance Bladder 43 0.085
32
P BRS047 Breast Cancer 97 0.079
33
P MSC005 Muscular Dystrophy 66 0.079
34
P NRP001 Neuropathy 56 0.079
35
CRT017 Cartilage Disease 54 0.079
36
c EXS019 Exostoses, Multiple, Type I 53 0.079
37
PLS007 Plasmodium Falciparum Malaria 52 0.079
38
KSH004 Kashin-Beck Disease 38 0.079
39
P OVR042 Ovarian Cancer 88 0.073
40
MLR004 Malaria 81 0.073
41
SPN209 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations 66 0.073
42
P HRP006 Herpes Simplex 65 0.073
43
HYP066 Hyperglycemia 61 0.073
44
TRM010 Traumatic Brain Injury 51 0.073
45
BRN071 Brain Injury 49 0.073
46
SKL017 Skeletal Dysplasias 40 0.073
47
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.073
48
P CLR023 Colorectal Cancer 99 0.067
49
P OST002 Osteoporosis 74 0.067
50
c MCP052 Mucopolysaccharidosis, Type Vi 67 0.067
51
GST092 Gastroesophageal Reflux 67 0.067
52
OST159 Osteogenic Sarcoma 66 0.067
53
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.067
54
P PRD008 Periodontitis 64 0.067
55
ATM095 Autoimmune Disease 62 0.067
56
EYD002 Eye Disease 58 0.067
57
IRN002 Iron Metabolism Disease 57 0.067
58
PNG002 Pain Agnosia 51 0.067
59
BNR002 Bone Resorption Disease 48 0.067
60
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.067
61
P BNG032 Benign Mesothelioma 46 0.067
62
DWR001 Dwarfism 44 0.067
63
P END039 Endodermal Sinus Tumor 44 0.067
64
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.067
65
TST018 Testicular Yolk Sac Tumor 39 0.067
66
c CHR087 Chronic Cystitis 34 0.067
67
RDT001 Radiation Cystitis 32 0.067
68
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.060
69
CRH001 Crohn's Disease 74 0.060
70
ULC004 Ulcerative Colitis 73 0.060
71
c THR092 Thrombophilia Due to Thrombin Defect 73 0.060
72
MSC157 Muscular Dystrophy, Duchenne Type 72 0.060
73
P MLT020 Multiple Sclerosis 72 0.060
74
P PHC003 Pheochromocytoma 71 0.060
75
DFC004 Deficiency Anemia 70 0.060
76
P AMY004 Amyloidosis 70 0.060
77
P ADN016 Adenocarcinoma 64 0.060
78
SKN016 Skin Disease 63 0.060
79
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.060
80
P FBR017 Fibrosarcoma 56 0.060
81
P INF037 Inflammatory Bowel Disease 54 0.060
82
P LTR001 Lateral Sclerosis 54 0.060
83
P AST007 Astrocytoma 51 0.060
84
TMT002 Temtamy Preaxial Brachydactyly Syndrome 50 0.060
85
ADR040 Adrenal Gland Pheochromocytoma 46 0.060
86
URT010 Ureteral Obstruction 45 0.060
87
URL001 Urolithiasis 45 0.060
88
CYT002 Cytokine Deficiency 42 0.060
89
BCK006 Back Pain 42 0.060
90
ALL014 Allergic Encephalomyelitis 38 0.060
91
MCP033 Mucopolysaccharidoses 38 0.060
92
P HPT023 Hepatocellular Carcinoma 100 0.052
93
P ALZ034 Alzheimer Disease 88 0.052
94
c HYP836 Hypercholesterolemia, Familial, 1 73 0.052
95
P KDN018 Kidney Disease 72 0.052
96
P LKM002 Leukemia 68 0.052
97
CST001 Costello Syndrome 68 0.052
98
CNN005 Connective Tissue Disease 68 0.052
99
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.052
100
P HYD006 Hydrocephalus 66 0.052
101
KRT019 Keratitis, Hereditary 65 0.052
102
PRT036 Peritonitis 64 0.052
103
NRM005 Neuromuscular Disease 64 0.052
104
P MST009 Mastocytosis 64 0.052
105
P CRN300 Coronary Heart Disease 1 63 0.052
106
c GLC092 Glaucoma, Primary Open Angle 62 0.052
107
P ESP024 Esophagitis 62 0.052
108
ALL026 Allergic Hypersensitivity Disease 62 0.052
109
P MYL006 Myeloid Leukemia 60 0.052
110
P BCL017 B-Cell Lymphoma 58 0.052
111
FBR047 Fibromyalgia 58 0.052
112
P URT039 Urticaria 58 0.052
113
DSS008 Disease of Mental Health 58 0.052
114
HYP266 Hypoxia 57 0.052
115
P PLY019 Polyneuropathy 56 0.052
116
CHR100 Chronic Ulcer of Skin 55 0.052
117
SNS003 Sensory Peripheral Neuropathy 54 0.052
118
PRS045 Prostatic Hypertrophy 53 0.052
119
P RTN016 Retinal Degeneration 53 0.052
120
c PSR017 Psoriasis 2 53 0.052
121
c MCR113 Microvascular Complications of Diabetes 3 52 0.052
122
c PSR023 Psoriasis 1 52 0.052
123
PPT001 Peptic Esophagitis 52 0.052
124
PRS021 Prostatic Adenoma 51 0.052
125
CLR109 Colorectal Adenocarcinoma 51 0.052
126
P OVR082 Overgrowth Syndrome 50 0.052
127
P TMP001 Temporal Lobe Epilepsy 50 0.052
128
KRT001 Keratoconjunctivitis Sicca 49 0.052
129
PRS129 Prostatic Hyperplasia, Benign 49 0.052
130
P OPN001 Open-Angle Glaucoma 49 0.052
131
BLD044 Bladder Disease 48 0.052
132
c PSR032 Psoriasis 11 47 0.052
133
c MCR120 Microvascular Complications of Diabetes 7 47 0.052
134
CHR074 Choriocarcinoma 47 0.052
135
EXS001 Exostosis 46 0.052
136
MDD018 Middle East Respiratory Syndrome 43 0.052
137
c PSR028 Psoriasis 7 42 0.052
138
OCL052 Ocular Dominance 42 0.052
139
c CFF007 Coffin-Siris Syndrome 2 41 0.052
140
c MCR130 Microvascular Complications of Diabetes 6 41 0.052
141
c MCR133 Microvascular Complications of Diabetes 4 41 0.052
142
c PSR018 Psoriasis 13 41 0.052
143
48X005 48,xyyy 39 0.052
144
P PRS040 Prostate Cancer 97 0.042
145
c LKM061 Leukemia, Acute Myeloid 84 0.042
146
CYS001 Cystic Fibrosis 81 0.042
147
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.042
148
P HRT032 Heart Disease 75 0.042
149
c MCP050 Mucopolysaccharidosis, Type Ii 72 0.042
150
DWN001 Down Syndrome 70 0.042
151
P OST001 Osteopetrosis 70 0.042
152
c CHR684 Chronic Kidney Disease 70 0.042
153
ADL002 Adult Syndrome 70 0.042
154
P MYP004 Myopathy 70 0.042
155
P TYS001 Tay-Sachs Disease 69 0.042
156
MST024 Mastocytosis, Cutaneous 69 0.042
157
P LVR013 Liver Disease 68 0.042
158
SKN019 Skin Melanoma 68 0.042
159
c INF071 Inflammatory Bowel Disease 1 67 0.042
160
BRK010 Burkitt Lymphoma 67 0.042
161
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.042
162
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.042
163
P PSD087 Pseudoxanthoma Elasticum 65 0.042
164
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.042
165
CLF027 Cleft Palate, Isolated 64 0.042
166
c MCP049 Mucopolysaccharidosis, Type Vii 63 0.042
167
LSH001 Leishmaniasis 63 0.042
168
CLT003 Colitis 62 0.042
169
P PLY014 Polycystic Kidney Disease 62 0.042
170
c BRN108 Branchiootic Syndrome 1 62 0.042
171
c MCP047 Mucopolysaccharidosis, Type Iva 61 0.042
172
NRL005 Neurilemmoma 60 0.042
173
P CTR002 Cataract 60 0.042
174
PLM033 Pulmonary Embolism 59 0.042
175
PRN019 Perinatal Necrotizing Enterocolitis 59 0.042
176
P MLN069 Melanoma, Uveal 59 0.042
177
GNG013 Gingivitis 59 0.042
178
IRN001 Iron Deficiency Anemia 59 0.042
179
P DNG005 Dengue Virus 59 0.042
180
ADN018 Adenoma 59 0.042
181
ISC004 Ischemia 58 0.042
182
P EHL001 Ehlers-Danlos Syndrome 58 0.042
183
c MCP004 Mucopolysaccharidosis Iv 57 0.042
184
P UVT001 Uveitis 57 0.042
185
c LKM070 Leukemia, Acute Monocytic 57 0.042
186
P BPL003 Bipolar Disorder 56 0.042
187
HMT008 Hematuria, Benign Familial 56 0.042
188
EXF001 Exfoliation Syndrome 56 0.042
189
SFT003 Soft Tissue Sarcoma 56 0.042
190
EMB004 Embryonal Carcinoma 56 0.042
191
INT030 Intracranial Aneurysm 56 0.042
192
AGN016 Aging 56 0.042
193
NPH009 Nephrolithiasis 55 0.042
194
P ART021 Arteriosclerosis 54 0.042
195
P EPD016 Epidermolysis Bullosa 53 0.042
196
KRT006 Keratoconjunctivitis 53 0.042
197
P MNC007 Monocytic Leukemia 53 0.042
198
CRH005 Crohn's Colitis 53 0.042
199
c PRD040 Periodontitis, Chronic 53 0.042
200
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.042
201
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.042
202
ACT200 Acute Monoblastic Leukemia 52 0.042
203
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.042
204
ENT011 Enterocolitis 51 0.042
205
SPN019 Spondylolisthesis 51 0.042
206
ENT004 Enthesopathy 49 0.042
207
BLL004 Bullous Keratopathy 49 0.042
208
47X002 47,xyy 49 0.042
209
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.042
210
DRY001 Dry Eye Syndrome 47 0.042
211
KRT008 Keratopathy 47 0.042
212
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.042
213
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.042
214
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.042
215
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.042
216
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.042
217
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.042
218
P CHR345 Chronic Pain 44 0.042
219
c PCH010 Pachyonychia Congenita 3 44 0.042
220
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.042
221
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.042
222
MYF002 Myofascial Pain Syndrome 42 0.042
223
c HYP057 Hypervitaminosis D 42 0.042
224
MLT162 Multiple Joint Dislocations, Short Stature, and Craniofacial Dysmorphism with or Without Congenital Heart Defects 42 0.042
225
P KLZ004 Kala-Azar 1 41 0.042
226
c MJR024 Major Affective Disorder 9 41 0.042
227
c EXS020 Exostoses, Multiple, Type Ii 40 0.042
228
KLD004 Keloid Disorder 40 0.042
229
c MJR022 Major Affective Disorder 8 38 0.042
230
P MRQ003 Morquio Syndrome 37 0.042
231
PLC006 Placental Choriocarcinoma 36 0.042
232
SPN331 Spondyloocular Syndrome 36 0.042
233
HRW001 Hair Whorl 36 0.042
234
c LKM005 Leukemia, T-Cell, Chronic 34 0.042
235
P DSB002 Desbuquois Dysplasia 32 0.042
236
EXN003 Exencephaly 31 0.042
237
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.042
238
ARG004 Argyria 27 0.042
239
URN022 Urinary Tract Infections, Recurrent 27 0.042
240
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.042
241
P LTH050 Lethal Chondrodysplasia 14 0.042
242
MYL069 Myeloma, Multiple 85 0.030
243
P PNC035 Pancreatic Cancer 84 0.030
244
NRL016 Neural Tube Defects 82 0.030
245
P GLM040 Glioma Susceptibility 1 81 0.030
246
P RHM011 Rheumatoid Arthritis 80 0.030
247
P BLD134 Bladder Cancer 79 0.030
248
P LKM071 Leukemia, Chronic Lymphocytic 79 0.030
249
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.030
250
P LNG064 Lung Cancer Susceptibility 3 78 0.030
251
P PRK057 Parkinson Disease, Late-Onset 78 0.030
252
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.030
253
AST005 Asthma 76 0.030
254
c ATR087 Atrial Standstill 1 75 0.030
255
END057 Endometrial Cancer 74 0.030
256
SVR004 Severe Combined Immunodeficiency 73 0.030
257
P CNR004 Cone-Rod Dystrophy 2 73 0.030
258
ANX010 Anxiety 73 0.030
259
c HPT073 Hepatitis C Virus 72 0.030
260
P HNT016 Huntington Disease 72 0.030
261
ACR007 Acromegaly 71 0.030
262
P EPL164 Epilepsy 71 0.030
263
P HYP061 Hypertrophic Cardiomyopathy 70 0.030
264
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.030
265
WRN001 Werner Syndrome 69 0.030
266
P LKM062 Leukemia, Acute Lymphoblastic 69 0.030
267
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.030
268
P LYM118 Lymphoma 68 0.030
269
ODN023 Odontochondrodysplasia 68 0.030
270
P SYS005 Systemic Scleroderma 68 0.030
271
SND001 Sandhoff Disease 68 0.030
272
c BSL007 Basal Cell Carcinoma 68 0.030
273
BRN024 Bronchitis 68 0.030
274
RCK004 Rickets 68 0.030
275
PNC129 Pancreatic Adenocarcinoma 68 0.030
276
P THR014 Thrombocytopenia 67 0.030
277
P CRD119 Cardiac Arrest 67 0.030
278
P HPT021 Hepatitis 67 0.030
279
CRP001 Carpal Tunnel Syndrome 67 0.030
280
P SKN015 Skin Carcinoma 66 0.030
281
MYX005 Myxoid Liposarcoma 66 0.030
282
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.030
283
ACH004 Achondroplasia 66 0.030
284
LBR036 Leber Plus Disease 66 0.030
286
P MNN013 Meningitis 66 0.030
287
P DRM053 Dermatitis, Atopic 66 0.030
288
P PLM036 Pulmonary Fibrosis 65 0.030
289
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.030
290
SRC014 Sarcoma 65 0.030
291
P LPS002 Liposarcoma 65 0.030
292
P MTR014 Motor Neuron Disease 65 0.030
293
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.030
294
PRT037 Pertussis 65 0.030
295
P CHR071 Charcot-Marie-Tooth Disease 65 0.030
296
APN008 Apnea, Obstructive Sleep 64 0.030
297
GT001 Gout 64 0.030
298
MSC007 Muscle Hypertrophy 64 0.030
299
OST017 Osteomyelitis 64 0.030
300
P RHB003 Rhabdomyosarcoma 63 0.030
301
P VSC007 Vascular Disease 63 0.030
302
c MLG084 Malignant Fibrous Histiocytoma 63 0.030
303
INT146 Intervertebral Disc Disease 63 0.030
304
P END044 Endometriosis 63 0.030
305
c ATM011 Autoimmune Hepatitis 63 0.030
306
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.030
307
LPD008 Lipid Metabolism Disorder 62 0.030
308
c FNC043 Fanconi Anemia, Complementation Group E 62 0.030
309
c HPT003 Hepatitis a 62 0.030
310
c SVR001 Severe Acute Respiratory Syndrome 62 0.030
311
P HYP750 Hypertriglyceridemia, Familial 62 0.030
312
P LRS001 Larsen Syndrome 62 0.030
313
LVR012 Liver Cirrhosis 62 0.030
314
CHL068 Cholestasis 61 0.030
315
P DRM010 Dermatomyositis 61 0.030
316
FTT001 Fatty Liver Disease 61 0.030
317
DRM006 Dermatitis 61 0.030
318
P ENC004 Encephalitis 61 0.030
319
P STS008 Sotos Syndrome 1 61 0.030
320
P PNC044 Pancreatitis 61 0.030
321
P SJG008 Sjogren Syndrome 61 0.030
322
RTN017 Retinal Detachment 61 0.030
323
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.030
324
P SCL018 Scoliosis 60 0.030
325
c ACT027 Acute Pancreatitis 60 0.030
326
RHM001 Rheumatic Fever 60 0.030
327
P USH001 Usher Syndrome 60 0.030
328
P MYC008 Myocarditis 59 0.030
329
CHL014 Cholera 59 0.030
330
IGR001 Ige Responsiveness, Atopic 59 0.030
331
c DNG003 Dengue Disease 59 0.030
332
P BRS044 Breast Adenocarcinoma 59 0.030
333
GRD007 Grade Iii Astrocytoma 59 0.030
334
P GLL022 Guillain-Barre Syndrome 59 0.030
335
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.030
336
ANR040 Aneurysm 59 0.030
337
PSD012 Pseudoachondroplasia 58 0.030
338
P ANP001 Anaplastic Large Cell Lymphoma 58 0.030
339
ANT024 Anthrax Disease 58 0.030
340
CNT047 Contact Dermatitis 58 0.030
341
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.030
342
BRS051 Breast Disease 58 0.030
343
P PRP019 Peripheral Nervous System Disease 58 0.030
344
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 57 0.030
345
P EXN002 Exanthem 57 0.030
346
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.030
347
LYM021 Lymphadenitis 57 0.030
348
P FCL005 Focal Segmental Glomerulosclerosis 57 0.030
349
TNS005 Tonsillitis 57 0.030
350
JPN002 Japanese Encephalitis 57 0.030
351
AYM001 Ayme-Gripp Syndrome 57 0.030
352
P ANG015 Angioedema 57 0.030
353
BCT022 Bacterial Infectious Disease 56 0.030
354
P SZR006 Seizure Disorder 56 0.030
355
ALL010 Allergic Contact Dermatitis 56 0.030
356
OVR012 Ovarian Serous Cystadenocarcinoma 56 0.030
357
PYC001 Pycnodysostosis 56 0.030
358
P GST044 Gastritis 56 0.030
359
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.030
360
HYP005 Hypokalemia 55 0.030
361
FND002 Fundus Dystrophy 55 0.030
362
P DRR001 Diarrhea 55 0.030
363
P GRV001 Graves' Disease 55 0.030
364
P LRY044 Larynx Cancer 55 0.030
365
P SLM003 Salmonellosis 55 0.030
366
CLF004 Cleft Lip/palate 54 0.030
367
GLS001 Gliosarcoma 54 0.030
368
AMN003 Amnestic Disorder 54 0.030
369
GLC003 Glucose Intolerance 54 0.030
370
MSC162 Muscular Dystrophy, Congenital Merosin-Deficient, 1a 54 0.030
371
MCL075 Macular Dystrophy, Corneal 54 0.030
372
TND005 Tendinitis 54 0.030
373
c MLG077 Malignant Peripheral Nerve Sheath Tumor 54 0.030
374
DBT010 Diabetic Neuropathy 54 0.030
375
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.030
376
RCS002 Recessive Dystrophic Epidermolysis Bullosa 54 0.030
377
P BRC006 Brachydactyly 53 0.030
378
P END047 Endophthalmitis 53 0.030
379
OST016 Osteochondrosis 53 0.030
380
P CTN003 Cutaneous Lupus Erythematosus 53 0.030
381
CLF001 Cleft Lip 53 0.030
382
SPN035 Spindle Cell Sarcoma 53 0.030
383
P ACT008 Actinic Keratosis 53 0.030
384
OVR059 Ovary Adenocarcinoma 53 0.030
385
P RTN018 Retinal Disease 53 0.030
386
DMY004 Demyelinating Disease 52 0.030
387
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 52 0.030
388
c MSC169 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 1 52 0.030
389
LYS002 Lysosomal Storage Disease 52 0.030
390
P DDN001 Duodenal Ulcer 52 0.030
391
P CNG436 Congenital Disorder of Deglycosylation 52 0.030
392
ART074 Aortic Dissection 52 0.030
393
P TRT010 Teratoma 52 0.030
394
PRV004 Periventricular Leukomalacia 52 0.030
395
c INH030 Inherited Retinal Disorder 51 0.030
396
NPH003 Nephrocalcinosis 51 0.030
397
KRT009 Keratosis 51 0.030
398
MYL001 Myelitis 51 0.030
399
PLS009 Plasma Cell Neoplasm 51 0.030
400
c PNC106 Pancreatic Agenesis 1 51 0.030
401
VSC006 Vascular Cancer 51 0.030
402
CLB002 Clubfoot 51 0.030
403
NRM004 Neuroma 51 0.030
404
BLL003 Bell's Palsy 51 0.030
405
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.030
406
HYP781 Hypoascorbemia 51 0.030
407
PLR008 Pleurisy 50 0.030
408
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.030
409
BRN009 Burning Mouth Syndrome 50 0.030
410
STM007 Stomatitis 50 0.030
411
P AGG001 Aggressive Periodontitis 50 0.030
412
P KRT007 Keratoconus 50 0.030
413
NTR046 Neutrophil Migration 50 0.030
414
P OTS001 Otosclerosis 49 0.030
415
P CRN025 Corneal Dystrophy 49 0.030
416
PLY024 Polymicrogyria 49 0.030
417
AMB002 Amblyopia 49 0.030
418
c ACH042 Achondrogenesis, Type Ib 49 0.030
419
BCT004 Bacteriuria 49 0.030
420
VCC001 Vaccinia 49 0.030
421
LRN003 Learning Disability 49 0.030
422
c DSB006 Desbuquois Dysplasia 1 48 0.030
423
ATS010 Autosomal Recessive Disease 48 0.030
424
CLS016 Clostridium Difficile Colitis 48 0.030
425
PNC034 Pancreas Disease 48 0.030
426
PYL006 Pyloric Stenosis 48 0.030
427
HLX001 Helix Syndrome 47 0.030
428
PPL002 Papillary Carcinoma 47 0.030
429
RNL077 Renal Fibrosis 47 0.030
430
KRT002 Keratomalacia 47 0.030
431
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.030
432
AML029 Ameloblastoma 46 0.030
433
CMP012 Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome 46 0.030
435
KRT013 Keratolytic Winter Erythema 46 0.030
436
TXC011 Toxocariasis 46 0.030
437
SCL002 Scleredema Adultorum 46 0.030
438
P HRD001 Hereditary Multiple Exostoses 46 0.030
439
SVN002 Sveinsson Chorioretinal Atrophy 46 0.030
440
MYX013 Myxofibrosarcoma 45 0.030
441
c GM2006 Gm2 Gangliosidosis 45 0.030
442
c ATM099 Autoimmune Uveitis 45 0.030
443
LRY022 Laryngoonychocutaneous Syndrome 44 0.030
444
CYS009 Cystadenoma 44 0.030
445
FCH001 Fuchs' Endothelial Dystrophy 44 0.030
446
SCH030 Schneckenbecken Dysplasia 44 0.030
447
P GNG009 Gangliosidosis 44 0.030
448
P FBR003 Fibrous Histiocytoma 44 0.030
449
DYS018 Dysostosis 44 0.030
450
FBR054 Fibroma 44 0.030
451
CHN010 Chondroma 43 0.030
452
SPN369 Spinal Disease 43 0.030
453
TND004 Tendinopathy 43 0.030
454
RFR003 Refractive Error 43 0.030
455
DYS032 Dystrophinopathies 43 0.030
456
P CRN026 Corneal Edema 43 0.030
457
P DMY001 Demyelinating Polyneuropathy 43 0.030
458
BCL002 B Cell Deficiency 43 0.030
459
PRS036 Parasitic Protozoa Infectious Disease 43 0.030
460
DSC009 Discoid Lupus Erythematosus 42 0.030
461
SNL007 Senile Cataract 42 0.030
462
c CNG023 Congenital Fibrosarcoma 42 0.030
463
ATX019 Ataxia with Vitamin E Deficiency 42 0.030
464
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.030
465
c MLG079 Malignant Pleural Mesothelioma 42 0.030
466
IDP070 Idiopathic Scoliosis 42 0.030
467
TND006 Tendinosis 42 0.030
468
EPC002 Epicondylitis 41 0.030
469
MNN002 Mononeuritis Multiplex 41 0.030
470
LCH016 Lichen Sclerosus Et Atrophicus 41 0.030
471
XRP001 Xerophthalmia 41 0.030
472
PLY183 Polymicrogyria with or Without Vascular-Type Ehlers-Danlos Syndrome 41 0.030
473
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.030
474
P HYP009 Hypertrophic Pyloric Stenosis 41 0.030
475
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.030
476
c HYP072 Hypersensitivity Reaction Type Iii Disease 40 0.030
477
BRS050 Breast Cyst 40 0.030
478
P MSC134 Musculocontractural Ehlers-Danlos Syndrome 40 0.030
479
WLL004 Wallerian Degeneration 39 0.030
480
SPP007 Suppression Amblyopia 39 0.030
481
P BRC003 Brachyolmia 39 0.030
482
c HRD104 Hereditary Multiple Osteochondromas 39 0.030
483
AML001 Amelanotic Melanoma 39 0.030
484
CRN288 Corneal Dystrophy, Band-Shaped 38 0.030
485
OVR094 Ovarian Epithelial Cancer 38 0.030
486
HPT070 Hepatosplenic T-Cell Lymphoma 38 0.030
487
DYS006 Dysembryoplastic Neuroepithelial Tumor 38 0.030
488
SHW001 Shwartzman Phenomenon 37 0.030
489
OPS002 Opsismodysplasia 37 0.030
490
DDN027 Duodenum Disease 37 0.030
491
GLM044 Glomerular Disease 37 0.030
492
WGN003 Wagner Syndrome 36 0.030
493
P AXN001 Axonal Neuropathy 36 0.030
495
PNC005 Penicilliosis 34 0.030
496
HMP018 Hemophilic Arthropathy 34 0.030
498
c PYL018 Pyloric Stenosis, Infantile Hypertrophic, 1 33 0.030
499
PPL052 Papillomatosis, Confluent and Reticulated 33 0.030
500
c SBC035 Subacute Cutaneous Lupus Erythematosus 32 0.030
501
SCL025 Scleromyxedema 32 0.030
502
ENC014 Enchondroma 29 0.030
504
P QLT011 Qualitative or Quantitative Defects of Sarcoglycan 26 0.030
505
MLG164 Malignant Epithelial Tumor of Ovary 26 0.030
506
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.030
507
PRN071 Parenteral Nutrition-Associated Cholestasis 25 0.030
508
OVR098 Ovarian Fibroma 25 0.030
509
MCN011 Mucinoses 24 0.030
510
DRM046 Dermal Ridges-off-the-End 24 0.030
511
CRN023 Corneal Deposit 22 0.030
512
CRT057 Critical Congenital Heart Disease 21 0.030
513
GLS013 Glossodynia 18 0.030
514
BRC114 Brachyolmia Type 1, Hobaek Type 17 0.030
515
CLF034 Cleft Hard Palate 16 0.030
516
SKL033 Skeletal Dysplasia, Mild, with Joint Laxity and Advanced Bone Age 12 0.030
517
MCP042 Mucopolysaccharidoses, Unclassified Types 10 0.030
Content
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