Search results for surfactant deficiency

441 hits were found for surfactant deficiency

# Family MCID Name MIFTS Score
1
c SRF003 Surfactant Metabolism Dysfunction, Pulmonary, 2 29 5.189
2
c SRF004 Surfactant Metabolism Dysfunction, Pulmonary, 1 29 4.873
3
SRF006 Surfactant Dysfunction 33 4.027
4
c SRF005 Surfactant Metabolism Dysfunction, Pulmonary, 3 28 3.913
5
c SRF008 Surfactant Metabolism Dysfunction, Pulmonary, 4 26 3.832
6
c SRF007 Surfactant Metabolism Dysfunction, Pulmonary, 5 22 3.816
7
c SFT007 Sftpc-Related Pulmonary Surfactant Metabolism Dysfunction 9 3.018
8
CSF003 Csfrb-Related Pulmonary Surfactant Metabolism Dysfunction 8 3.018
9
c SFT005 Sftpb-Related Pulmonary Surfactant Metabolism Dysfunction 9 2.898
10
c ABC006 Abca3-Related Pulmonary Surfactant Metabolism Dysfunction 9 2.430
11
PLM066 Pulmonary Surfactant Protein B, Deficiency of 5 1.890
12
LNG099 Lung Disease 64 0.247
13
PRT011 Protein C Deficiency 52 0.213
14
P PNM007 Pneumonia 68 0.213
15
CHL071 Child Syndrome 58 0.190
16
c ACT210 Acute Respiratory Distress Syndrome 57 0.190
17
KDS001 Kid Syndrome 53 0.190
18
MCN007 Meconium Aspiration Syndrome 52 0.189
19
NTR005 Nutritional Deficiency Disease 36 0.189
20
P ADL010 Adult Respiratory Distress Syndrome 61 0.188
21
RSP019 Respiratory Distress Syndrome in Premature Infants 43 0.179
22
P RSP003 Respiratory Failure 71 0.173
23
P THY032 Thyroiditis 54 0.172
24
RSP006 Respiratory System Disease 58 0.169
25
PRT014 Protein S Deficiency 53 0.166
26
NWB001 Newborn Respiratory Distress Syndrome 45 0.164
27
RSP007 Respiratory Distress Syndrome, Infant 22 0.160
28
CHR322 Choreoathetosis, Hypothyroidism, and Neonatal Respiratory Distress 40 0.155
29
INT066 Interstitial Lung Disease 59 0.153
30
c ADL080 Adult Acute Respiratory Distress Syndrome 19 0.146
31
P PLM006 Pulmonary Alveolar Proteinosis 48 0.146
32
P INF038 Influenza 72 0.144
33
P AST005 Asthma 82 0.143
34
P PLM036 Pulmonary Fibrosis 71 0.138
35
CYS001 Cystic Fibrosis 83 0.138
36
THR024 Thrombosis 57 0.138
37
BRN056 Bronchopulmonary Dysplasia 48 0.138
38
TBR010 Tuberculosis 70 0.134
39
P LNG032 Lung Cancer 95 0.133
40
ADL002 Adult Syndrome 52 0.130
41
P ADN016 Adenocarcinoma 69 0.125
42
P HPT021 Hepatitis 69 0.120
43
CRB009 Cerebritis 39 0.119
44
ATH003 Atherosclerosis 65 0.110
45
NNT004 Neonatal Respiratory Failure 37 0.109
46
ALR002 Al-Raqad Syndrome 36 0.109
47
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.107
48
P ART022 Arthritis 75 0.106
49
P PLM071 Pulmonary Surfactant Metabolism Dysfunction 35 0.105
50
NSD001 Nose Disease 48 0.102
51
P LKM002 Leukemia 71 0.101
52
c INH020 Inherited Metabolic Disorder 49 0.101
53
DRM006 Dermatitis 66 0.100
54
PNM008 Pneumothorax 53 0.097
55
P OBS005 Obesity 92 0.096
56
TRC026 Tracheal Disease 35 0.095
57
P RHM011 Rheumatoid Arthritis 89 0.095
58
END072 Endotheliitis 42 0.095
59
P NRP001 Neuropathy 59 0.092
60
ACD009 Acid-Labile Subunit, Deficiency of 45 0.091
61
PLM034 Pulmonary Emphysema 55 0.090
62
PLC008 Placenta Disease 33 0.085
63
PRS047 Prostatitis 56 0.084
64
CSY001 C Syndrome 50 0.083
65
C3D001 C3 Deficiency 53 0.083
66
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.082
67
P LPS004 Lupus Erythematosus 64 0.082
68
P SHR029 Short Syndrome 58 0.080
69
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.080
70
P HRT032 Heart Disease 75 0.079
71
ISC004 Ischemia 61 0.078
72
P INF032 Infertility 59 0.077
73
c PLM150 Pulmonary Alveolar Proteinosis, Acquired 23 0.077
74
c SYS001 Systemic Lupus Erythematosus 86 0.077
75
c AST037 Asthma 1 28 0.077
76
ALL026 Allergic Hypersensitivity Disease 52 0.076
77
PCK002 Pick Disease 68 0.076
78
MSS002 Mass Syndrome 48 0.076
79
PRV004 Periventricular Leukomalacia 48 0.075
80
LKM006 Leukomalacia 43 0.075
81
BRN002 Bronchiolitis 56 0.075
82
PRT056 Protein R Deficiency 10 0.075
83
PLM010 Pulmonary Edema 54 0.074
84
P CNG015 Congenital Diaphragmatic Hernia 60 0.074
85
P LYM118 Lymphoma 69 0.074
86
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 36 0.074
87
c CNG121 Congenital Pulmonary Alveolar Proteinosis 14 0.073
88
P INF037 Inflammatory Bowel Disease 63 0.073
89
P THL005 Thalassemia 64 0.073
90
P PNC044 Pancreatitis 61 0.072
91
PLM033 Pulmonary Embolism 60 0.072
92
P PLM037 Pulmonary Hypertension 79 0.072
93
HMT018 Hematopoietic Stem Cell Transplantation 41 0.072
94
ATP002 Atopy 66 0.072
95
RTN018 Retinal Disease 53 0.070
96
LPD004 Lipoid Nephrosis 48 0.070
97
BLD054 Blood Protein Disease 37 0.070
98
BRN038 Bronchial Disease 51 0.070
99
c AST039 Asthma 2 28 0.069
100
P KDN018 Kidney Disease 66 0.069
101
PLM001 Pulmonary Tuberculosis 67 0.069
102
SKN016 Skin Disease 66 0.068
103
CNT047 Contact Dermatitis 61 0.068
104
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 54 0.068
105
P HYP086 Hypothyroidism 64 0.068
106
P MNN013 Meningitis 67 0.067
107
ATN011 Autoinflammation with Infantile Enterocolitis 39 0.067
108
SKN023 Skin Tag 44 0.066
109
PRN019 Perinatal Necrotizing Enterocolitis 42 0.066
110
P ASP006 Aspergillosis 61 0.066
111
DMN002 Dementia 65 0.065
112
CLT003 Colitis 60 0.065
113
ACR041 Acromelic Frontonasal Dysostosis 45 0.065
114
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.064
115
ALL006 Allergic Asthma 58 0.064
116
SLC006 Silicosis 53 0.064
117
IMM136 Immune System Disease 51 0.064
118
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.063
119
CLD014 Cole Disease 37 0.063
120
CHL068 Cholestasis 59 0.063
121
BRT030 Birth Defects 43 0.062
122
P RHN004 Rhinitis 60 0.062
123
BRN071 Brain Injury 52 0.061
124
P ATP001 Atopic Dermatitis 62 0.061
125
LRY017 Laryngeal Disease 34 0.061
126
WLL006 Wells Syndrome 59 0.061
127
GDS001 Good Syndrome 44 0.061
128
SCK005 Sickle Cell Disease 51 0.061
129
P HMN010 Hemangioma 59 0.060
130
CRN246 Cranioosteoarthropathy 31 0.060
131
DRG003 Drug Dependence 50 0.060
132
CCN007 Cocoon Syndrome 45 0.059
133
ART002 Arts Syndrome 51 0.058
134
CHL079 Children's Interstitial Lung Disease 18 0.058
135
ACQ007 Acquired Immunodeficiency Syndrome 60 0.058
136
P ESN008 Eosinophilic Pneumonia 51 0.058
137
P PSR002 Psoriasis 61 0.058
138
P ICH004 Ichthyosis 52 0.057
139
ADJ001 Adjustment Disorder 38 0.057
140
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.056
141
c THR092 Thrombophilia Due to Thrombin Defect 54 0.056
142
P HRM001 Hermansky-Pudlak Syndrome 59 0.056
143
OLG003 Oligohydramnios 53 0.055
144
STC004 Stachybotrys Chartarum 37 0.055
145
PLM129 Pulmonary Disease, Chronic Obstructive 63 0.055
146
VND001 Vein Disease 47 0.055
147
OTT002 Otitis Media 66 0.055
148
P SPS003 Spastic Diplegia 52 0.055
149
ATN005 Autonomic Dysfunction 49 0.055
150
P DRR001 Diarrhea 60 0.055
151
c CRN214 Coronary Heart Disease 5 22 0.055
152
P TRN020 Turner Syndrome 65 0.054
153
ALL010 Allergic Contact Dermatitis 57 0.054
154
SKN027 Skin Conditions 43 0.054
155
HYP711 Hypotonia, Ataxia, and Delayed Development Syndrome 26 0.054
156
CNN005 Connective Tissue Disease 62 0.054
157
PRD011 Proud Syndrome 42 0.054
158
HYP266 Hypoxia 56 0.054
159
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.054
160
MCS002 Mucositis 55 0.053
161
VGN023 Vaginitis 42 0.053
162
ADN018 Adenoma 58 0.053
163
IDP011 Idiopathic Interstitial Pneumonia 56 0.053
164
UPP004 Upper Respiratory Tract Disease 46 0.053
165
ATN002 Autonomic Nervous System Disease 48 0.052
166
NSY001 N Syndrome 36 0.052
167
VNT001 Ventilation Pneumonitis 35 0.052
168
CRB037 Cerebral Palsy 66 0.052
169
NRM005 Neuromuscular Disease 56 0.052
170
STM006 Stomach Disease 50 0.052
171
PLM012 Pulmonary Sarcoidosis 54 0.051
172
P PRD008 Periodontitis 63 0.051
173
c EHL032 Ehlers-Danlos Syndrome, Type Viib 49 0.051
174
NNS002 Nonspecific Interstitial Pneumonia 45 0.051
175
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.050
176
BRN022 Bronchiectasis 50 0.050
177
P PRS040 Prostate Cancer 90 0.050
178
THL010 Thalassemia Minor 39 0.050
179
WST001 West Syndrome 57 0.050
180
c HPT001 Hepatitis C 68 0.049
181
c CNG027 Congenital Hemolytic Anemia 48 0.049
182
ALL003 Allergic Rhinitis 63 0.049
183
BRN012 Bronchiolitis Obliterans 58 0.049
184
CHR005 Chorioamnionitis 48 0.049
185
c CNT068 Central Pain Syndrome 29 0.049
186
DBT010 Diabetic Neuropathy 55 0.049
187
VCC001 Vaccinia 46 0.049
188
P HRP006 Herpes Simplex 65 0.048
189
RBR001 Roberts Syndrome 60 0.048
190
ANG049 Angioedema Induced by Ace Inhibitors 34 0.048
191
BCK006 Back Pain 43 0.048
192
CML001 Cumulative Trauma Disorders 18 0.048
193
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.048
194
P CHR345 Chronic Pain 50 0.048
195
MTH009 Mouth Disease 61 0.048
196
ULC004 Ulcerative Colitis 76 0.047
197
EYD002 Eye Disease 61 0.047
198
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.047
199
P DRM010 Dermatomyositis 62 0.047
200
CHL123 Chlamydia 60 0.047
201
PRP019 Peripheral Nervous System Disease 55 0.047
202
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.047
203
c TRC078 Trichohepatoenteric Syndrome 2 29 0.047
204
SML020 Small Patella Syndrome 36 0.046
205
P LYM026 Lymphoblastic Leukemia 62 0.046
206
HYP458 Hyper Ige Syndrome 42 0.046
207
VSC047 Vascular Malformation 45 0.046
208
P PLY019 Polyneuropathy 56 0.046
209
c HMG001 Hemoglobin C Disease 47 0.046
210
DWN001 Down Syndrome 66 0.045
211
EXT034 Extrinsic Allergic Alveolitis 54 0.045
212
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 40 0.045
213
P OCY001 Oocyte Maturation Defect 38 0.045
214
GLB003 Globe Disease 32 0.045
215
c CNG006 Congenital Hypothyroidism 60 0.045
216
HMG005 Hemoglobinopathy 52 0.045
217
BLM001 Bloom Syndrome 63 0.045
218
PLR022 Pleural Disease 51 0.044
219
c VRL005 Viral Pneumonia 42 0.044
220
SCL017 Sclerosing Hemangioma 41 0.044
221
GLS018 Glass Syndrome 34 0.044
222
c SCN051 Secondary Pulmonary Alveolar Proteinosis 18 0.044
223
c CHR096 Chronic Pulmonary Heart Disease 40 0.044
224
HYD012 Hydrops Fetalis 43 0.044
225
P CRN178 Coronary Heart Disease 6 21 0.044
226
P GLB002 Glioblastoma 68 0.043
227
MLN007 Male Infertility 55 0.043
228
TTH006 Tooth Disease 52 0.043
229
CYT002 Cytokine Deficiency 30 0.043
230
c SVR001 Severe Acute Respiratory Syndrome 57 0.043
231
CRB085 Cerebral Hemorrhage 46 0.043
232
c CRN173 Coronary Heart Disease 8 18 0.043
233
SCK003 Sickle Cell Anemia 71 0.043
234
P GT001 Gout 58 0.043
235
GLC008 Glucose Metabolism Disease 42 0.043
236
c CRN175 Coronary Heart Disease 4 19 0.043
237
c CRN172 Coronary Heart Disease 3 19 0.042
238
P ALX003 Alexander Disease 63 0.042
239
WLL001 Williams-Beuren Syndrome 60 0.042
240
DPH001 Diphtheria 59 0.042
241
P TMT001 Timothy Syndrome 55 0.042
242
PNM001 Pneumocystosis 50 0.042
243
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.042
244
CNT067 Central Cord Syndrome 23 0.042
245
VSC007 Vascular Disease 67 0.042
246
HV1006 Hiv-1 80 0.041
247
GLC037 Glucocorticoid Resistance 62 0.041
248
P EXN002 Exanthem 57 0.041
249
CYT008 Cytomegalovirus Infection 52 0.041
250
PRM025 Primary Bacterial Infectious Disease 41 0.041
251
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.041
252
PLS010 Plasma Protein Metabolism Disease 34 0.041
253
SBS003 Substance Abuse 54 0.041
254
c LRG001 Large Cell Carcinoma 51 0.041
255
ACT017 Acute Chest Syndrome 48 0.041
256
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.041
257
P CHR071 Charcot-Marie-Tooth Disease 67 0.040
258
c HPT003 Hepatitis a 59 0.040
259
CRY005 Cryptococcosis 50 0.040
260
LRN003 Learning Disability 49 0.040
261
P AXN001 Axonal Neuropathy 38 0.040
262
ATM012 Autoimmune Disease of Blood 35 0.040
263
SQM006 Squamous Cell Carcinoma 70 0.040
264
BRC012 Brucellosis 66 0.040
265
NRT004 Neuritis 52 0.040
266
P LYM007 Lymphangioleiomyomatosis 66 0.039
267
PLN006 Poland Syndrome 54 0.039
268
P PLY041 Polymyositis 52 0.039
269
BLL003 Bell's Palsy 48 0.039
270
DCB001 Decubitus Ulcer 41 0.039
271
ATR003 Atrophic Rhinitis 31 0.039
272
BRW006 Brown Syndrome 29 0.039
273
LPD027 Lip Disease 28 0.039
274
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.039
275
PRP027 Peripheral Vascular Disease 68 0.039
276
OLV001 Olivopontocerebellar Atrophy 53 0.039
277
ANG011 Angiodysplasia 44 0.039
278
c HMG003 Hemoglobin E Disease 44 0.039
279
CRB031 Cerebral Arterial Disease 27 0.039
280
LSH001 Leishmaniasis 66 0.038
281
TXC005 Toxic Shock Syndrome 60 0.038
282
EXF001 Exfoliation Syndrome 57 0.038
283
BNF002 Bone Fracture 50 0.038
284
P PLN008 Peeling Skin Syndrome 45 0.038
285
ATM052 Autoimmune Disease 1 25 0.038
286
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.037
287
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.037
288
P TBR001 Tuberous Sclerosis 67 0.037
289
P UVT001 Uveitis 58 0.037
290
DMY004 Demyelinating Disease 53 0.037
291
P TCL004 T-Cell Leukemia 47 0.037
292
STF001 Stiff-Person Syndrome 56 0.037
293
P ALL008 Allergic Bronchopulmonary Aspergillosis 51 0.037
294
P PLM040 Pulmonary Valve Disease 43 0.037
295
FCT008 Factitious Disorder 41 0.037
296
HRT012 Heart Valve Disease 40 0.037
297
PLM018 Pulmonary Sclerosing Hemangioma 39 0.037
298
LNS003 Lens Disease 33 0.037
299
c PLM127 Pulmonary Hypertension, Primary, 3 28 0.037
300
PLM124 Pulmonary Hypertension, Neonatal 22 0.037
301
WSC001 Wisconsin Syndrome 14 0.037
302
P RTT002 Rett Syndrome 77 0.037
303
ART005 Arteriovenous Malformation 66 0.037
304
KRT001 Keratoconjunctivitis Sicca 59 0.037
305
LYM019 Lymphosarcoma 53 0.037
306
P HRD018 Hair Disease 51 0.037
307
MSL001 Measles 61 0.036
308
c ACT073 Acute Leukemia 60 0.036
309
ASP003 Aseptic Meningitis 51 0.036
310
GST078 Gastrointestinal Allergy 40 0.036
311
c PLN018 Peeling Skin Syndrome 2 40 0.036
312
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 37 0.036
313
c HYP595 Hypertension, Essential 69 0.035
314
c ADL017 Adult T-Cell Leukemia 60 0.035
315
DRY001 Dry Eye Syndrome 50 0.035
316
THL018 Thalassemia Major 48 0.035
317
ADR038 Adermatoglyphia 46 0.035
318
SNS003 Sensory Peripheral Neuropathy 45 0.035
319
P ART084 Arteriovenous Fistula 44 0.035
320
GST092 Gastroesophageal Reflux 62 0.034
321
P SNS014 Sinusitis 60 0.034
322
PNC034 Pancreas Disease 58 0.034
323
GNR004 Generalized Anxiety Disorder 51 0.034
324
P SJG001 Sjogren's Syndrome 50 0.034
325
c INV001 Invasive Aspergillosis 47 0.034
326
SLV003 Salivary Gland Disease 47 0.034
327
WBR001 Weber Syndrome 41 0.034
328
ADT003 Auditory System Disease 40 0.034
329
c ADL001 Adult Lymphoma 39 0.034
330
NRP016 Neuropathy, Recurrent, with Pressure Palsies 38 0.034
331
LCR008 Lacrimal Apparatus Disease 37 0.034
332
c DRR009 Diarrhea 6 29 0.034
333
c AST050 Asthma, Phf11-Related 22 0.034
334
ATM053 Autoimmune Disease 2 16 0.034
335
ATM054 Autoimmune Disease 3 15 0.034
336
P LNG064 Lung Cancer Susceptibility 3 62 0.033
337
GLL022 Guillain-Barre Syndrome 56 0.033
338
c MLG077 Malignant Peripheral Nerve Sheath Tumor 56 0.033
339
GNT003 Genital Herpes 53 0.033
340
THL016 Thalassemias, Alpha- 53 0.033
341
TLN003 Telangiectasis 52 0.033
342
NRP015 Neuropathy, Congenital Hypomyelinating 52 0.033
343
P CFF001 Coffin-Siris Syndrome 51 0.033
344
RSS002 Roussy-Levy Syndrome 50 0.033
345
c CHR532 Charcot-Marie-Tooth Disease, Type 2e 49 0.033
346
P TRC086 Trichohepatoenteric Syndrome 1 48 0.033
347
BRD001 Brody Myopathy 47 0.033
348
PLY020 Polyradiculoneuropathy 45 0.033
349
HRT015 Heritable Pulmonary Arterial Hypertension 45 0.033
350
IRR003 Irritant Dermatitis 44 0.033
351
BHR001 Behr Syndrome 42 0.033
352
P CHR102 Charcot-Marie-Tooth Neuropathy 41 0.033
353
THL017 Thalassemia Intermedia 40 0.033
354
HMG025 Hemoglobin H Disease, Nondeletional 39 0.033
355
PDT001 Pediatric Lymphoma 38 0.033
356
c PNC106 Pancreatic Agenesis 1 37 0.033
357
EXC003 Excessive Tearing 36 0.033
358
LCN001 Lice Infestation 31 0.033
359
c CRN176 Coronary Heart Disease 9 18 0.033
360
ATM055 Autoimmune Disease 4 15 0.033
361
MLD001 Melioidosis 67 0.031
362
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 60 0.031
363
P PNM006 Pneumoconiosis 51 0.031
364
c CHR537 Charcot-Marie-Tooth Disease, Type 1e 50 0.031
365
c CHR527 Charcot-Marie-Tooth Disease, Type 1b 49 0.031
366
SLD003 Sialadenitis 49 0.031
367
LMB062 Limb Ischemia 48 0.031
368
P RNL017 Renal Oncocytoma 47 0.031
369
P OTT001 Otitis Externa 47 0.031
370
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 46 0.031
371
DJR004 Dejerine-Sottas Disease 46 0.031
372
P ICH001 Ichthyosis Vulgaris 46 0.031
373
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.031
374
MTR007 Motor Peripheral Neuropathy 37 0.031
375
c CHR520 Charcot-Marie-Tooth Disease, Axonal, Type 2s 36 0.031
376
c HRD094 Hereditary Motor and Sensory Neuropathy, Type Iic 34 0.031
377
IMM039 Immune Hydrops Fetalis 33 0.031
378
ATM059 Autoimmune Disease 6 22 0.031
379
P GNR027 Generalized Peeling Skin Syndrome 19 0.031
380
P PLZ001 Pelizaeus-Merzbacher Disease 65 0.030
381
BRN024 Bronchitis 64 0.030
382
P SYS005 Systemic Scleroderma 61 0.030
383
P MCR129 Microvascular Complications of Diabetes 1 54 0.030
384
NRL005 Neurilemmoma 51 0.030
385
FRM003 Farmer's Lung 47 0.030
386
DBT008 Diabetic Angiopathy 44 0.030
387
STT002 Status Asthmaticus 42 0.030
388
c CHR530 Charcot-Marie-Tooth Disease, Type 2b 40 0.030
389
c HRD088 Hereditary Neuropathies 40 0.030
390
HNZ001 Heinz Body Anemia 39 0.030
391
P CHR348 Charcot-Marie-Tooth Neuropathy, X-Linked Dominant, 1 38 0.030
392
c CHR534 Charcot-Marie-Tooth Disease, Type 1d 38 0.030
393
c CHR407 Charcot-Marie-Tooth Disease, Type 4f 38 0.030
394
LNG013 Lung Lymphoma 38 0.030
395
c DBT048 Diabetes Mellitus, Insulin-Dependent, 11 36 0.030
396
RHB002 Rhabdoid Meningioma 36 0.030
397
PLM052 Pulmonary Arteriovenous Malformation 34 0.030
398
ALV006 Alveolar Capillary Dysplasia 33 0.030
399
FTD001 Foot Drop 33 0.030
400
PRN029 Parainfluenza Virus Type 3 31 0.030
401
MN1001 Mn1 30 0.030
402
c STR092 Striatal Degeneration, Autosomal Dominant 2 27 0.030
403
PLM134 Pulmonary Fibrosis, Idiopathic 61 0.028
404
c MNN043 Meningioma, Familial 59 0.028
405
c CHR536 Charcot-Marie-Tooth Disease, Type 1a 58 0.028
406
CHR177 Chromophobe Renal Cell Carcinoma 56 0.028
407
AVN001 Avian Influenza 54 0.028
408
HPT009 Hepatopulmonary Syndrome 48 0.028
409
SPN021 Spinal Meningioma 44 0.028
410
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 42 0.028
411
ASB001 Asbestosis 42 0.028
412
HYD038 Hydrops Fetalis, Nonimmune 40 0.028
413
CHR100 Chronic Ulcer of Skin 40 0.028
414
c ACT004 Acute Diarrhea 39 0.028
415
ALP093 Alpha-Thalassemia/mental Retardation Syndrome, Chromosome 16-Related 37 0.028
416
c CHR535 Charcot-Marie-Tooth Disease, Type 1c 37 0.028
417
BRC011 Brachial Plexus Neuropathy 36 0.028
418
c CHR533 Charcot-Marie-Tooth Disease, Type 1f 36 0.028
419
c DBT058 Diabetes Mellitus, Insulin-Dependent, 7 35 0.028
420
c DBT054 Diabetes Mellitus, Insulin-Dependent, 24 34 0.028
421
ALT002 Aleutian Mink Disease 33 0.028
422
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 33 0.028
423
P ACT080 Acute Pulmonary Heart Disease 31 0.028
424
c NRV012 Nervous System Benign Neoplasm 31 0.028
425
c DRR007 Diarrhea 7 31 0.028
426
c CHR113 Charcot-Marie-Tooth Neuropathy Type 1 31 0.028
427
ISC001 Ischemic Neuropathy 30 0.028
428
ALP094 Alpha Thalassemia-Intellectual Disability Syndrome Type 1 29 0.028
429
MTH064 Methemoglobinemia, Beta-Globin Type 29 0.028
430
SPL009 Splenic Sequestration 28 0.028
431
TYP027 Type 1 Diabetes Mellitus 10 27 0.028
432
AMY003 Amyotrophic Neuralgia 27 0.028
433
c CHR352 Charcot-Marie-Tooth Disease, Axonal, Type 2f 27 0.028
434
IMM002 Immature Cataract 27 0.028
435
c ATM007 Autoimmune Disease of Central Nervous System 25 0.028
436
PRM133 Primary Pulmonary Lymphoma 23 0.028
437
c CHR313 Charcot-Marie-Tooth Neuropathy Type 4f 19 0.028
438
VSC009 Vascular Skin Disease 19 0.028
439
CNG102 Congenital Hypomyelination Neuropathy 18 0.028
440
c SML023 Small Cell Lung Cancer, Adult 15 0.028
441
c ATP019 Atopic Dermatitis 6 14 0.028
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