Search results for Pulmonary Surfactants

685 hits were found for Pulmonary Surfactants

# Family MCID Name MIFTS Score
1
c SRF003 Surfactant Metabolism Dysfunction, Pulmonary, 2 36 7.916
2
P SRF004 Surfactant Metabolism Dysfunction, Pulmonary, 1 38 7.722
3
c SRF005 Surfactant Metabolism Dysfunction, Pulmonary, 3 34 6.338
4
c SRF008 Surfactant Metabolism Dysfunction, Pulmonary, 4 31 6.322
5
c SRF007 Surfactant Metabolism Dysfunction, Pulmonary, 5 23 6.302
6
SRF006 Surfactant Dysfunction 35 6.000
7
c PRM166 Primary Interstitial Lung Disease Specific to Childhood Due to Pulmonary Surfactant Protein Anomalies 8 3.961
8
PLM066 Pulmonary Surfactant Protein B, Deficiency of 1 2.317
9
P PLM037 Pulmonary Hypertension 68 1.014
10
LNG099 Lung Disease 61 0.980
11
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.969
12
PLM001 Pulmonary Tuberculosis 70 0.964
13
PLM033 Pulmonary Embolism 59 0.793
14
IDP011 Idiopathic Interstitial Pneumonia 63 0.787
15
P PLM036 Pulmonary Fibrosis 61 0.783
16
P RSP003 Respiratory Failure 74 0.745
17
PLM010 Pulmonary Edema 55 0.643
18
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.588
19
PLM134 Pulmonary Fibrosis, Idiopathic 75 0.585
20
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.563
21
BRN056 Bronchopulmonary Dysplasia 57 0.521
22
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.513
23
PNM008 Pneumothorax 56 0.511
24
INT066 Interstitial Lung Disease 59 0.462
25
P ADL010 Adult Respiratory Distress Syndrome 63 0.439
26
P MYC084 Mycobacterium Tuberculosis 1 68 0.434
27
NWB001 Newborn Respiratory Distress Syndrome 58 0.434
28
RSP019 Respiratory Distress Syndrome in Premature Infants 57 0.421
29
P PNM007 Pneumonia 68 0.402
30
P PTN014 Patent Ductus Arteriosus 1 60 0.402
31
P SRC025 Sarcoidosis 1 70 0.377
32
P PLM006 Pulmonary Alveolar Proteinosis 52 0.374
33
P PLM034 Pulmonary Emphysema 56 0.369
34
P ASP006 Aspergillosis 66 0.351
35
P ADN016 Adenocarcinoma 64 0.347
36
CYS001 Cystic Fibrosis 80 0.345
37
BRN024 Bronchitis 68 0.342
38
HRT011 Heart Septal Defect 50 0.337
39
MCN007 Meconium Aspiration Syndrome 52 0.316
40
P LNG032 Lung Cancer 97 0.316
41
P VSC007 Vascular Disease 63 0.314
42
HYP266 Hypoxia 56 0.311
43
P HRT032 Heart Disease 75 0.298
44
BRN002 Bronchiolitis 59 0.290
45
P VNT002 Ventricular Septal Defect 60 0.280
46
c DPH024 Diaphragmatic Hernia, Congenital 64 0.277
47
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.267
48
P HYP098 Hypereosinophilic Syndrome 66 0.267
49
P TTR001 Tetralogy of Fallot 69 0.264
50
c SCL052 Scleroderma, Familial Progressive 62 0.261
51
PLM012 Pulmonary Sarcoidosis 53 0.259
52
c THR092 Thrombophilia Due to Thrombin Defect 73 0.258
53
INT011 Interstitial Emphysema 34 0.257
54
CNG034 Congestive Heart Failure 70 0.255
55
AST005 Asthma 77 0.254
56
P BRN022 Bronchiectasis 59 0.251
57
48X005 48,xyyy 39 0.249
58
ADL002 Adult Syndrome 69 0.249
59
P CRD119 Cardiac Arrest 67 0.245
60
P LNG064 Lung Cancer Susceptibility 3 77 0.234
61
RSP007 Respiratory Distress Syndrome, Infant 30 0.231
62
c HYP595 Hypertension, Essential 84 0.226
63
ALL026 Allergic Hypersensitivity Disease 64 0.225
64
THR024 Thrombosis 56 0.221
65
SLC006 Silicosis 56 0.220
66
CNN005 Connective Tissue Disease 66 0.219
67
CYT002 Cytokine Deficiency 44 0.219
68
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.216
69
ANR040 Aneurysm 58 0.213
70
c BCT013 Bacterial Pneumonia 47 0.211
71
ENT011 Enterocolitis 50 0.207
72
CYN002 Cyanosis, Transient Neonatal 45 0.206
73
c PLM022 Pulmonary Valve Insufficiency 40 0.203
74
c EXD008 Exudative Vitreoretinopathy 1 69 0.203
75
PNM010 Pneumothorax, Primary Spontaneous 60 0.198
76
PRN019 Perinatal Necrotizing Enterocolitis 54 0.196
77
P SYS005 Systemic Scleroderma 70 0.195
78
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.192
79
ISC004 Ischemia 60 0.192
80
CHD004 Chudley-Mccullough Syndrome 44 0.191
81
ANT018 Anthracosis 48 0.186
82
HLX001 Helix Syndrome 47 0.186
83
P INF038 Influenza 68 0.185
84
BRN012 Bronchiolitis Obliterans 56 0.183
85
EXT034 Extrinsic Allergic Alveolitis 58 0.182
86
47X002 47,xyy 49 0.181
87
P PNM006 Pneumoconiosis 55 0.180
88
P VSC011 Vasculitis 62 0.180
89
P ESN008 Eosinophilic Pneumonia 50 0.180
90
CRY005 Cryptococcosis 58 0.174
91
TXC005 Toxic Shock Syndrome 61 0.170
92
P SLP006 Sleep Apnea 69 0.170
93
BCT022 Bacterial Infectious Disease 56 0.167
94
ACQ007 Acquired Immunodeficiency Syndrome 60 0.163
95
IMM167 Immune Deficiency Disease 78 0.162
96
P NTR004 Neutropenia 63 0.161
97
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.160
98
HMP009 Haemophilus Influenzae 42 0.157
99
PLM035 Pulmonary Eosinophilia 48 0.156
100
ALL006 Allergic Asthma 56 0.155
101
NNS002 Nonspecific Interstitial Pneumonia 45 0.155
102
HMN044 Human Immunodeficiency Virus Type 1 71 0.153
103
ADN018 Adenoma 58 0.153
104
ACT029 Acute Interstitial Pneumonia 44 0.151
105
P LPS004 Lupus Erythematosus 61 0.151
106
OTT002 Otitis Media 71 0.150
107
LYM007 Lymphangioleiomyomatosis 68 0.150
108
P ACT105 Acute Mountain Sickness 52 0.148
109
ATM095 Autoimmune Disease 61 0.147
110
c SML038 Small Cell Cancer of the Lung 65 0.147
111
c SYS001 Systemic Lupus Erythematosus 86 0.146
112
P AMY004 Amyloidosis 70 0.141
113
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.141
114
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.140
115
P RHN004 Rhinitis 57 0.137
116
P LYM118 Lymphoma 68 0.136
117
PNM001 Pneumocystosis 54 0.135
118
c PLM150 Pulmonary Alveolar Proteinosis, Acquired 40 0.135
119
c INV001 Invasive Aspergillosis 48 0.135
120
GST092 Gastroesophageal Reflux 65 0.132
121
SDD001 Sudden Infant Death Syndrome 61 0.132
122
ASP007 Aspiration Pneumonia 48 0.131
123
ASB001 Asbestosis 46 0.131
124
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.131
125
ASB003 Asbestos Intoxication 26 0.131
126
P RHM011 Rheumatoid Arthritis 80 0.131
127
NNT004 Neonatal Respiratory Failure 35 0.130
128
P SCK005 Sickle Cell Disease 50 0.130
129
OST159 Osteogenic Sarcoma 66 0.130
130
PLM017 Pulmonary Alveolar Microlithiasis 50 0.130
131
DRM006 Dermatitis 61 0.130
132
P BNG032 Benign Mesothelioma 45 0.129
133
CRD137 Cardiogenic Shock 48 0.128
134
c ACT027 Acute Pancreatitis 59 0.127
135
SQM006 Squamous Cell Carcinoma 60 0.127
136
P ALL008 Allergic Bronchopulmonary Aspergillosis 53 0.127
137
P KDN018 Kidney Disease 70 0.126
138
c LRG001 Large Cell Carcinoma 49 0.126
139
LNG031 Lung Benign Neoplasm 50 0.126
140
P ENC018 Encephalopathy 61 0.125
141
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.124
142
PLY150 Polykaryocytosis Inducer 31 0.124
143
P SML001 Small Cell Carcinoma 52 0.123
144
P PNC044 Pancreatitis 61 0.123
145
PRV004 Periventricular Leukomalacia 51 0.121
146
P HMN010 Hemangioma 61 0.121
147
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.120
148
PLM032 Pulmonary Blastoma 46 0.120
149
PRT037 Pertussis 65 0.120
150
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.119
151
PNG002 Pain Agnosia 51 0.119
152
P HYP086 Hypothyroidism 68 0.119
153
ATH013 Atherosclerosis Susceptibility 66 0.119
154
P CLR023 Colorectal Cancer 98 0.118
155
P HYP055 Hypoplastic Left Heart Syndrome 62 0.118
156
P DRM010 Dermatomyositis 61 0.118
157
AGN016 Aging 56 0.117
158
CHL123 Chlamydia 59 0.117
159
PRT036 Peritonitis 65 0.117
160
MTB004 Metabolic Acidosis 50 0.115
161
P DBT009 Diabetes Mellitus 64 0.115
162
CHR005 Chorioamnionitis 51 0.114
163
BRN014 Bronchopneumonia 50 0.114
164
P TRC086 Trichohepatoenteric Syndrome 1 59 0.114
165
c SPN225 Spondyloarthropathy 1 73 0.114
166
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.113
167
ASP008 Aspiration Pneumonitis 42 0.112
168
DFC004 Deficiency Anemia 75 0.112
169
c ATR087 Atrial Standstill 1 74 0.112
170
ALL003 Allergic Rhinitis 67 0.111
171
THR013 Thoracic Outlet Syndrome 53 0.111
172
CNT047 Contact Dermatitis 57 0.110
173
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.110
174
P BRS047 Breast Cancer 96 0.110
175
DWN001 Down Syndrome 70 0.109
176
P LKM002 Leukemia 66 0.109
177
c DNT047 Dentinogenesis Imperfecta Type 2 33 0.109
178
ANX010 Anxiety 72 0.109
179
OLG003 Oligohydramnios 52 0.108
180
c PRC016 Pre-Eclampsia 63 0.107
181
P INF037 Inflammatory Bowel Disease 56 0.107
182
P TBR001 Tuberous Sclerosis 70 0.107
183
OCL069 Ocular Motor Apraxia 51 0.106
184
CRB037 Cerebral Palsy 68 0.106
185
P CLL015 Collagen Disease 42 0.106
186
ATX019 Ataxia with Vitamin E Deficiency 48 0.106
187
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.106
188
THY029 Thyroid Carcinoma 59 0.106
189
P LYM031 Lymphocytic Leukemia 55 0.105
190
CHR074 Choriocarcinoma 46 0.105
191
HRW001 Hair Whorl 36 0.105
192
SVR004 Severe Combined Immunodeficiency 73 0.105
193
P PLM182 Pulmonary Hypoplasia, Primary 32 0.105
194
BRN015 Bronchiolo-Alveolar Adenocarcinoma 54 0.105
195
ESP021 Esophageal Cancer 90 0.104
196
P PLY041 Polymyositis 57 0.104
197
CCC001 Coccidioidomycosis 53 0.104
198
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 20 0.103
199
SCH014 Schistosomiasis 56 0.103
200
SCL017 Sclerosing Hemangioma 32 0.103
201
P BCL017 B-Cell Lymphoma 58 0.102
202
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.102
203
c ACT071 Acute Kidney Failure 59 0.102
204
P MYC007 Myocardial Infarction 70 0.100
205
PRT011 Protein C Deficiency 45 0.100
206
P TRN020 Turner Syndrome 65 0.100
207
c CNG121 Congenital Pulmonary Alveolar Proteinosis 18 0.100
208
c PLM044 Pulmonary Fibrosis, Familial 23 0.100
209
INT304 Interstitial Pneumonitis, Desquamative, Familial 45 0.100
210
P HYD006 Hydrocephalus 65 0.099
211
P GRF003 Graft-Versus-Host Disease 71 0.099
212
ULC004 Ulcerative Colitis 73 0.099
213
PLM018 Pulmonary Sclerosing Hemangioma 35 0.098
214
c MST023 Mesothelioma, Malignant 57 0.097
215
MXD005 Mixed Connective Tissue Disease 59 0.097
216
ALC007 Alcohol Dependence 66 0.096
217
IRN002 Iron Metabolism Disease 57 0.096
218
PRQ002 Paraquat Poisoning 25 0.096
219
P PSR002 Psoriasis 62 0.095
220
P CND004 Candidiasis 57 0.095
221
PST011 Pustulosis of Palm and Sole 52 0.095
222
P HRM001 Hermansky-Pudlak Syndrome 65 0.095
223
c VRL005 Viral Pneumonia 49 0.094
224
HPT009 Hepatopulmonary Syndrome 49 0.094
225
P HRP006 Herpes Simplex 65 0.094
226
GLB015 Glioblastoma Multiforme 75 0.094
227
P DRR001 Diarrhea 57 0.094
228
MLN008 Melanoma 69 0.092
229
ANR007 Anorexia Nervosa 63 0.092
230
ATS010 Autosomal Recessive Disease 48 0.092
231
P THL005 Thalassemia 60 0.092
232
PLM013 Pulmonary Immaturity 29 0.092
233
NTR046 Neutrophil Migration 50 0.092
234
P LVR013 Liver Disease 68 0.091
235
ARG004 Argyria 28 0.091
236
c SCN051 Secondary Pulmonary Alveolar Proteinosis 22 0.091
237
P DRM053 Dermatitis, Atopic 66 0.090
238
PLR022 Pleural Disease 44 0.090
239
P NRB001 Neuroblastoma 71 0.090
240
LSH001 Leishmaniasis 63 0.089
241
P KLZ004 Kala-Azar 1 41 0.089
242
DSS009 Disseminated Intravascular Coagulation 57 0.089
243
c FNC043 Fanconi Anemia, Complementation Group E 62 0.089
244
DYS073 Dysphagia 50 0.089
245
ART140 Arteries, Anomalies of 53 0.089
246
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.088
247
ACN002 Acanthosis Nigricans 60 0.088
248
ANX004 Anoxia 42 0.088
249
P ANR048 Aniridia 1 63 0.088
250
CLT003 Colitis 62 0.088
251
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.088
252
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.088
253
DFF002 Diffuse Pulmonary Fibrosis 29 0.087
254
ATX010 Ataxia Neuropathy Spectrum 38 0.087
255
ACT064 Acute Necrotizing Encephalitis 32 0.087
256
BLD137 Blood Group--Ahonen 19 0.087
257
HYP066 Hyperglycemia 61 0.087
258
CRH001 Crohn's Disease 74 0.087
259
IGR001 Ige Responsiveness, Atopic 59 0.087
260
CHL147 Chlamydia Pneumonia 45 0.087
261
KRT002 Keratomalacia 48 0.087
262
CHL079 Children's Interstitial Lung Disease 27 0.087
263
c RHB024 Rhabdomyosarcoma 2 65 0.087
264
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.087
265
PST092 Posttransplant Acute Limbic Encephalitis 29 0.087
266
P ANG001 Angelman Syndrome 67 0.086
267
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.085
268
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.085
269
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.085
270
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.085
271
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.085
272
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.085
273
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.085
274
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.085
275
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.085
276
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.085
277
DPR016 Depression 63 0.085
278
IRR003 Irritant Dermatitis 47 0.085
279
CHL014 Cholera 55 0.085
280
SCK003 Sickle Cell Anemia 72 0.084
281
P HYP061 Hypertrophic Cardiomyopathy 66 0.084
282
ALL010 Allergic Contact Dermatitis 55 0.084
283
P LKM062 Leukemia, Acute Lymphoblastic 68 0.084
284
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 53 0.083
285
c CHR684 Chronic Kidney Disease 66 0.083
286
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.082
287
OST017 Osteomyelitis 64 0.082
288
c SVR001 Severe Acute Respiratory Syndrome 55 0.082
289
GLS018 Glass Syndrome 53 0.081
290
LPD008 Lipid Metabolism Disorder 62 0.081
291
SPN186 Spinal Cord Injury 60 0.081
292
P MNN013 Meningitis 65 0.081
293
PPT005 Peptic Ulcer Disease 58 0.081
294
PRS030 Persistent Fetal Circulation Syndrome 52 0.081
295
c HRD171 Hereditary Pulmonary Alveolar Proteinosis 35 0.080
296
HYD038 Hydrops Fetalis, Nonimmune 61 0.080
297
c LKM061 Leukemia, Acute Myeloid 83 0.080
298
PNB004 Panbronchiolitis, Diffuse 37 0.080
299
c TBR025 Tuberous Sclerosis 1 76 0.080
300
SKN016 Skin Disease 63 0.079
301
P ALC033 Alcohol Use Disorder 58 0.078
302
P RHB003 Rhabdomyosarcoma 62 0.078
303
P GST044 Gastritis 55 0.078
304
PRP027 Peripheral Vascular Disease 71 0.078
305
P NRP001 Neuropathy 56 0.078
306
CHL068 Cholestasis 60 0.077
307
MSL001 Measles 61 0.077
308
CYT008 Cytomegalovirus Infection 56 0.077
309
AND002 Androgen Insensitivity Syndrome 66 0.076
310
P AXN002 Axenfeld-Rieger Syndrome 58 0.076
311
ALR002 Al-Raqad Syndrome 34 0.076
312
ASP004 Asphyxia Neonatorum 45 0.076
313
P SJG008 Sjogren Syndrome 56 0.075
314
VRL011 Viral Infectious Disease 61 0.075
315
P TRT010 Teratoma 51 0.075
316
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.075
317
P PNC035 Pancreatic Cancer 84 0.075
318
HYP056 Hypoglycemia 66 0.075
319
NTR005 Nutritional Deficiency Disease 61 0.075
320
c HYP836 Hypercholesterolemia, Familial, 1 72 0.074
321
DPH001 Diphtheria 60 0.074
322
ATR057 Atrioventricular Block 55 0.074
323
P GLM045 Glioma 63 0.073
324
GLL048 Glial Tumor 45 0.073
325
HDN002 Head Injury 45 0.073
326
VCC001 Vaccinia 49 0.073
327
P OVR082 Overgrowth Syndrome 50 0.073
328
BRN038 Bronchial Disease 53 0.073
329
STC004 Stachybotrys Chartarum 34 0.072
330
STN013 Stenotrophomonas Maltophilia Infection 25 0.072
331
P ART023 Arthropathy 62 0.072
332
c MLG079 Malignant Pleural Mesothelioma 42 0.072
333
HYP081 Hypolipoproteinemia 50 0.072
334
P GST053 Gastric Cancer 83 0.072
335
PLM031 Poliomyelitis 57 0.072
336
OST012 Osteoarthritis 78 0.071
337
HYP060 Hyperinsulinism 54 0.071
338
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.071
339
BRN101 Bronchiolitis Obliterans with Obstructive Pulmonary Disease 28 0.071
340
KRT019 Keratitis, Hereditary 67 0.070
341
P ATX030 Ataxia-Telangiectasia 83 0.070
342
CHR100 Chronic Ulcer of Skin 53 0.070
343
ACT017 Acute Chest Syndrome 50 0.070
344
VSC003 Visceral Leishmaniasis 55 0.070
345
CHC001 Chickenpox 60 0.069
346
RHM027 Rheumatic Disease 56 0.069
347
P SZR006 Seizure Disorder 58 0.069
348
ART001 Arterial Tortuosity Syndrome 66 0.069
349
PRT082 Preterm Premature Rupture of the Membranes 54 0.069
350
ALB002 Albinism 46 0.068
351
IRN001 Iron Deficiency Anemia 58 0.068
353
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.067
354
P LYM033 Lymphoproliferative Syndrome 60 0.067
355
MLD001 Melioidosis 67 0.067
356
P PRP019 Peripheral Nervous System Disease 57 0.067
357
ISC020 Ischiocoxopodopatellar Syndrome with or Without Pulmonary Arterial Hypertension 41 0.067
358
c PRM038 Primary Agammaglobulinemia 43 0.066
359
P PRD008 Periodontitis 62 0.066
360
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.066
361
P HPT021 Hepatitis 67 0.066
362
P OCL002 Oculocutaneous Albinism 60 0.066
363
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.066
364
HYP005 Hypokalemia 55 0.065
365
IMP005 Impotence 52 0.065
366
c CHR682 Chronic Bilirubin Encephalopathy 38 0.065
367
P GCH001 Gaucher's Disease 64 0.065
368
c HPT016 Hepatitis B 59 0.064
369
ADN009 Adenosquamous Carcinoma 49 0.064
370
MLR004 Malaria 80 0.064
371
CRP001 Carpal Tunnel Syndrome 67 0.064
372
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.064
373
P UVT001 Uveitis 57 0.064
374
P ALP106 Alport Syndrome 1, X-Linked 55 0.064
375
P THY032 Thyroiditis 53 0.064
376
c ACT068 Acute Cystitis 63 0.064
377
P MYS005 Myositis 56 0.063
378
HNS001 Hansen's Disease 34 0.063
379
c SVR005 Severe Pre-Eclampsia 49 0.063
380
PPL052 Papillomatosis, Confluent and Reticulated 34 0.063
381
P LPR021 Leprosy 3 67 0.063
382
P TCL004 T-Cell Leukemia 47 0.062
383
RRD056 Rare Disease in Surgical Orthopedic 28 0.062
384
PNC129 Pancreatic Adenocarcinoma 67 0.061
385
STF001 Stiff-Person Syndrome 60 0.061
386
BRN071 Brain Injury 49 0.061
387
MTH071 Methane Production 26 0.061
388
PLC008 Placenta Disease 49 0.061
389
c GCH015 Gaucher Disease, Type I 70 0.061
390
P GLY013 Glycogen Storage Disease 59 0.061
391
c ACT134 Acute Liver Failure 51 0.060
392
CLR109 Colorectal Adenocarcinoma 50 0.060
393
BLR008 Bilirubin Metabolic Disorder 57 0.060
394
BYS001 Byssinosis 28 0.060
395
P ACR001 Aicardi-Goutieres Syndrome 65 0.060
396
BRR014 Barrett Esophagus 64 0.060
397
PRP016 Paraplegia 53 0.060
398
c ACR116 Aicardi-Goutieres Syndrome 1 51 0.060
399
PPL018 Papillary Adenocarcinoma 46 0.060
400
TLR001 Tularemia 49 0.059
401
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.059
402
P PRS040 Prostate Cancer 97 0.059
403
P OVR042 Ovarian Cancer 89 0.059
404
P LCT001 Lactic Acidosis 51 0.059
405
INS024 Insulin-Like Growth Factor I 79 0.059
406
CLN015 Colon Adenocarcinoma 63 0.059
407
P MYS003 Myasthenia Gravis 68 0.059
408
TST014 Testicular Cancer 46 0.059
409
OBS524 Obsolete: Benign Exophthalmos Syndrome 15 0.059
410
VSL002 Visual Epilepsy 58 0.058
411
P MLT020 Multiple Sclerosis 72 0.058
412
c BLD140 Blood Group, I System 30 0.058
413
CNS004 Constipation 57 0.058
414
GT001 Gout 63 0.058
415
GLC003 Glucose Intolerance 54 0.057
416
LWC002 Lowe Oculocerebrorenal Syndrome 66 0.057
417
ATN011 Autoinflammation with Infantile Enterocolitis 43 0.057
418
STM007 Stomatitis 49 0.057
419
BCT021 Bacterial Sepsis 44 0.057
420
LPD001 Lipid Pneumonia 27 0.057
421
P LTR001 Lateral Sclerosis 53 0.056
422
PLY012 Polyhydramnios 46 0.056
423
LYM019 Lymphosarcoma 47 0.056
424
GRM010 Germ Cells Tumors 34 0.056
425
FRM003 Farmer's Lung 40 0.056
426
SBC001 Subacute Sclerosing Panencephalitis 52 0.055
427
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 50 0.055
428
HPT019 Hepatic Encephalopathy 60 0.055
429
P AST007 Astrocytoma 50 0.055
430
HPT004 Hepatic Coma 43 0.055
431
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.055
432
MYC087 Mycoplasma Pneumoniae Pneumonia 50 0.055
433
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.055
434
PLM108 Pulmonary Interstitial Glycogenosis 17 0.055
435
HYP014 Hyperuricemia 51 0.055
436
RNL077 Renal Fibrosis 47 0.055
437
PPL001 Papillary Adenoma 45 0.054
438
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 59 0.054
439
c MGR028 Migraine with or Without Aura 1 69 0.054
440
P NRF023 Neurofibromatosis, Type Ii 76 0.054
441
P CNR004 Cone-Rod Dystrophy 2 71 0.054
442
c ADL017 Adult T-Cell Leukemia 57 0.054
443
P NMN002 Niemann-Pick Disease 60 0.053
444
PLG002 Plague 57 0.053
445
SMN007 Seminoma 44 0.053
446
AVN001 Avian Influenza 56 0.053
447
P SKN015 Skin Carcinoma 67 0.053
448
TXC007 Toxic Pneumonitis 29 0.053
449
CRV035 Cervical Cancer 76 0.053
450
P INF032 Infertility 57 0.053
451
BLD163 Blood Group, Dombrock System 26 0.053
452
GLC022 Glucose/galactose Malabsorption 45 0.052
453
P PYL005 Pyelonephritis 56 0.052
454
PRP080 Peripheral Artery Disease 53 0.052
455
PLC007 Placental Abruption 48 0.052
456
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.052
457
BLR001 Biliary Atresia 50 0.052
458
PLR025 Pleuroparenchymal Fibroelastosis 22 0.052
459
P DMN002 Dementia 67 0.051
460
TTN003 Tetanus 64 0.051
461
P RBL001 Rubella 58 0.051
462
ANT024 Anthrax Disease 58 0.051
463
TRM010 Traumatic Brain Injury 53 0.051
464
c CNG006 Congenital Hypothyroidism 65 0.051
465
FBR047 Fibromyalgia 59 0.051
466
P DDN001 Duodenal Ulcer 50 0.051
467
SML019 Smallpox 56 0.051
468
INT071 Intestinal Perforation 45 0.051
469
PST010 Pasteurellosis 33 0.050
470
EYD002 Eye Disease 58 0.050
471
LYS002 Lysosomal Storage Disease 52 0.050
472
CHL067 Cholecystitis 58 0.050
473
P HYP265 Hypotonia 42 0.050
474
ACT088 Acute Insulin Response 41 0.050
475
ENT001 Enterocele 39 0.050
476
PLR005 Pleuropneumonia 32 0.050
477
PLC005 Placental Insufficiency 57 0.050
478
PLL012 Pollen Allergy 45 0.050
479
P PRK057 Parkinson Disease, Late-Onset 76 0.049
480
CHL065 Cholangiocarcinoma 67 0.049
481
P CHR345 Chronic Pain 50 0.049
482
RRP031 Rare Pulmonary Disease 14 0.049
483
MCS002 Mucositis 55 0.049
485
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.049
486
PPL002 Papillary Carcinoma 47 0.049
487
GNG013 Gingivitis 59 0.049
488
GST033 Gestational Diabetes 57 0.049
489
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.048
490
BLD165 Blood Group, Colton System 23 0.048
491
FTT001 Fatty Liver Disease 61 0.048
492
CMB003 Combined T Cell and B Cell Immunodeficiency 52 0.048
493
P CMP008 Compartment Syndrome 48 0.048
494
ATM052 Autoimmune Disease 1 37 0.048
495
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.047
496
STT002 Status Asthmaticus 49 0.047
497
BRN028 Brain Cancer 73 0.047
498
c MCL062 Mucolipidosis Ii Alpha/beta 66 0.047
499
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.047
500
QFV001 Q Fever 58 0.047
501
INT079 Intrahepatic Cholangiocarcinoma 50 0.047
502
P GND004 Gonadal Dysgenesis 49 0.047
503
GST045 Gastroenteritis 59 0.046
504
P MLT074 Multiple Endocrine Neoplasia 55 0.046
505
CRP002 Croup 42 0.046
506
LPD009 Lipid Storage Disease 48 0.046
507
PLT015 Platelet Aggregation, Spontaneous 37 0.046
508
PLL001 Pallister-Hall Syndrome 64 0.046
509
AMN001 Amenorrhea 54 0.046
510
c CNT035 Central Nervous System Disease 54 0.046
511
INH001 Inhalation Anthrax 40 0.046
512
KLB003 Klebsiella Pneumonia 39 0.046
513
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 57 0.046
514
VRL003 Variola Major 43 0.045
515
SWN001 Swine Influenza 42 0.045
516
HMT002 Hematologic Cancer 62 0.045
517
PRS047 Prostatitis 56 0.045
518
BRN004 Brain Edema 55 0.045
519
P BRY005 Beryllium Disease 40 0.045
520
P PTT014 Pitt-Hopkins Syndrome 60 0.045
521
CRH005 Crohn's Colitis 52 0.045
522
RSP021 Respiratory Allergy 45 0.045
523
49X006 49, Xxxxy Syndrome 41 0.045
524
HRY003 Hairy Cell Leukemia 55 0.044
525
SPP010 Suppressor of Tumorigenicity 3 51 0.044
526
c HRM005 Hermansky-Pudlak Syndrome 1 50 0.044
527
c ADL080 Adult Acute Respiratory Distress Syndrome 26 0.044
528
HLC007 Helicobacter Pylori Infection 59 0.043
529
LYS003 Lysinuric Protein Intolerance 56 0.043
530
PNM005 Pneumonic Plague 50 0.043
531
SKN019 Skin Melanoma 67 0.043
532
P BRS044 Breast Adenocarcinoma 59 0.043
533
ANT017 Anthracosilicosis 23 0.043
534
LCN001 Lice Infestation 42 0.043
535
ATR003 Atrophic Rhinitis 33 0.043
536
P NRV007 Nervous System Disease 66 0.042
537
c LCL006 Localized Scleroderma 62 0.042
538
P MTC069 Mitochondrial Disorders 56 0.042
539
ICH001 Ichthyosis Vulgaris 55 0.042
540
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 27 0.042
541
OBS507 Obsolete: Small Pox 22 0.042
542
STR103 Streptococcus Pneumonia 45 0.042
543
SND001 Sandhoff Disease 68 0.041
544
c LNG109 Lung Cancer Susceptibility 1 26 0.041
545
VNT001 Ventilation Pneumonitis 23 0.041
546
CHR468 Chronic Pneumonitis of Infancy 14 0.041
547
PDC002 Pediculus Humanus Capitis Infestation 30 0.040
548
P MCK013 Meckel Syndrome, Type 1 65 0.040
549
P SNS001 Sensorineural Hearing Loss 61 0.040
550
P HYP083 Hypopituitarism 53 0.040
551
P MRC003 Mercury Poisoning 48 0.040
552
VGN023 Vaginitis 55 0.039
553
P MNC007 Monocytic Leukemia 54 0.039
554
ASP003 Aseptic Meningitis 51 0.039
555
RSP002 Respiratory Syncytial Virus Infectious Disease 51 0.039
556
GNT003 Genital Herpes 54 0.039
557
c HYP543 Hypoplastic Left Heart Syndrome 1 40 0.039
558
c MCR129 Microvascular Complications of Diabetes 1 66 0.039
559
RFS006 Refsum Disease, Classic 63 0.039
560
c HPT003 Hepatitis a 63 0.039
561
CTN007 Cutaneous Leishmaniasis 61 0.039
562
ACT058 Active Peptic Ulcer Disease 55 0.039
563
c PRD040 Periodontitis, Chronic 54 0.039
564
CHR073 Choreatic Disease 52 0.039
565
DDN006 Duodenitis 48 0.039
566
PRL019 Prolidase Deficiency 46 0.039
567
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 46 0.039
568
PLM179 Pulmonary Alveolar Proteinosis with Hypogammaglobulinemia 14 0.039
569
P EPL164 Epilepsy 71 0.038
570
DCB001 Decubitus Ulcer 60 0.038
571
ORL011 Oral Cancer 60 0.038
572
MST005 Mastitis 53 0.038
573
c MLG068 Malignant Glioma 45 0.038
574
P MXL015 Maxillary Sinusitis 37 0.038
575
RSC001 Rosacea 55 0.037
576
DNT012 Dental Caries 51 0.037
577
MTC005 Mitochondrial Metabolism Disease 48 0.037
578
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.037
579
BP1002 Bap1 Tumor Predisposition Syndrome 41 0.037
580
HYP193 Hypocomplementemic Urticarial Vasculitis 32 0.037
581
PTN004 Patent Ductus Venosus 27 0.037
582
NRN023 Neuroendocrine Cell Hyperplasia of Infancy 18 0.037
583
PRQ001 Paraquat Lung 16 0.037
584
P RTT002 Rett Syndrome 80 0.036
585
P LCH002 Lichen Planus 54 0.036
586
GSG001 Gas Gangrene 50 0.036
587
SLD003 Sialadenitis 50 0.036
588
BHR001 Behr Syndrome 49 0.036
589
c PRM093 Premature Ovarian Failure 7 47 0.036
590
FNG004 Fungal Meningitis 42 0.036
591
P TRC031 Trichorhinophalangeal Syndrome 40 0.036
592
CMP003 Compensatory Emphysema 24 0.036
593
P LKD001 Leukodystrophy 59 0.036
594
LCR013 Lacrimal Duct Defect 41 0.036
595
ACY011 Acyl-Coa Dehydrogenase Deficiency 37 0.036
596
HND015 Hand Skill, Relative 33 0.036
597
APN006 Apnea of Prematurity 23 0.036
598
P DNG005 Dengue Virus 57 0.034
599
P ICH004 Ichthyosis 54 0.034
600
KRT009 Keratosis 53 0.034
601
RYS001 Reye Syndrome 51 0.034
602
P PRR002 Pure Red-Cell Aplasia 48 0.034
603
c HYD019 Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius 47 0.034
604
c HYP793 Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 44 0.034
605
GNG011 Gingival Disease 44 0.034
606
RDC006 Red Cell Aplasia 42 0.034
607
STL007 Steel Syndrome 42 0.034
608
CRB079 Cerebrospinal Fluid Leak 35 0.034
609
PLN026 Pilonidal Sinus 35 0.034
610
c MLT160 Multiple Endocrine Neoplasia, Type Iia 69 0.033
611
ANN002 Anencephaly 55 0.033
612
LRN003 Learning Disability 49 0.033
613
DRY001 Dry Eye Syndrome 47 0.033
614
EBL001 Ebola Hemorrhagic Fever 46 0.033
615
PTT037 Pituitary Tumors 44 0.033
616
CRB004 Cerebral Artery Occlusion 44 0.033
617
ALL014 Allergic Encephalomyelitis 39 0.033
618
LRY004 Laryngotracheitis 31 0.033
619
CHR058 Chronic Congestive Splenomegaly 27 0.033
620
P MTC003 Metachromatic Leukodystrophy 70 0.032
621
P NRM002 Normal Pressure Hydrocephalus 56 0.032
622
JPN002 Japanese Encephalitis 54 0.032
623
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.032
624
MDD010 Middle Ear Disease 46 0.032
625
SPP008 Suppurative Otitis Media 45 0.032
626
P LTH003 Lethal Congenital Contracture Syndrome 42 0.032
627
PRN029 Parainfluenza Virus Type 3 36 0.032
628
SCR024 Sacrococcygeal Teratoma 29 0.032
629
PCK003 Pick Disease of Brain 68 0.031
630
c NMN013 Niemann-Pick Disease, Type a 62 0.031
631
P HYP035 Hypophosphatasia 60 0.031
632
CHR177 Chromophobe Renal Cell Carcinoma 56 0.031
633
DBT010 Diabetic Neuropathy 55 0.031
634
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 53 0.031
635
OCL006 Ocular Hypertension 53 0.031
636
MLT134 Multiple Pterygium Syndrome, Lethal Type 50 0.031
637
P INT099 Intrahepatic Cholestasis of Pregnancy 49 0.031
638
P DCR003 Dacryoadenitis 45 0.031
639
PDT025 Pediatric Multiple Sclerosis 36 0.031
640
ANT066 Anterior Cutaneous Nerve Entrapment Syndrome 31 0.031
643
ANG005 Anogenital Venereal Wart 56 0.029
644
P MLN007 Male Infertility 56 0.029
645
MSC190 Muscular Disease 51 0.029
646
CRN027 Corneal Neovascularization 47 0.029
647
NSS002 Neisseria Meningitidis Infection 46 0.029
648
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 46 0.029
649
c PCH010 Pachyonychia Congenita 3 43 0.029
650
OVR063 Overnutrition 43 0.029
651
DBT002 Diabetic Autonomic Neuropathy 41 0.029
652
P HRD144 Hereditary Mixed Polyposis Syndrome 39 0.029
653
FML039 Female Reproductive System Disease 38 0.029
654
MST021 Meester-Loeys Syndrome 33 0.029
655
CHR081 Choroideremia 57 0.028
656
P RNL017 Renal Oncocytoma 53 0.028
657
c LTN004 Late-Onset Retinal Degeneration 52 0.028
658
DRM011 Dermatophytosis 52 0.028
659
APL002 Aplasia of Lacrimal and Salivary Glands 50 0.028
660
P KRT007 Keratoconus 49 0.028
661
c MCK032 Meckel Syndrome, Type 3 49 0.028
662
FRS012 First-Degree Atrioventricular Block 41 0.028
663
CLP005 Ciliopathy 40 0.028
664
P OTT001 Otitis Externa 39 0.028
665
c CHR630 Chorea, Benign Hereditary 38 0.028
666
MLC004 Mulchandani-Bhoj-Conlin Syndrome 32 0.028
667
RHS001 Rh Isoimmunization 32 0.028
668
ADN014 Adenomatoid Tumor 30 0.028
669
P KRB001 Krabbe Disease 69 0.026
670
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.026
671
INT303 Intracranial Hypertension, Idiopathic 56 0.026
672
CLN045 Colonic Benign Neoplasm 49 0.026
673
MLT152 Multiple Self-Healing Squamous Epithelioma 48 0.026
674
c HYD064 Hydrocephalus, Congenital, 1 47 0.026
675
TNP001 Tinea Pedis 47 0.026
676
GLY031 Glycoproteinosis 46 0.026
677
P LBY004 Labyrinthitis 43 0.026
678
DPH021 Diaphragm Disease 43 0.026
679
PCD001 Pica Disease 37 0.026
680
P DCR004 Dacryocystitis 35 0.026
681
c PRM316 Primary Congenital Hypothyroidism 32 0.026
682
FTL029 Fetal Thalidomide Syndrome 27 0.026
683
URT049 Urate Oxidase, Pseudogene 25 0.026
684
LNR005 Linear Scleroderma 23 0.026
685
P INT354 Interstitial Lung Disease Specific to Childhood 8 0.026
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