Search results for "surfactant deficiency"

The MalaCard for "surfactant deficiency" has been retired.
Searching MalaCards for entries containing "surfactant deficiency"

379 hits were found for 'surfactant deficiency'

# Family MCID Name MIFTS Score
1
c SRF003 Surfactant Metabolism Dysfunction, Pulmonary, 2 29 5.188
2
c SRF004 Surfactant Metabolism Dysfunction, Pulmonary, 1 29 4.873
3
SRF006 Surfactant Dysfunction 33 4.034
4
c SRF005 Surfactant Metabolism Dysfunction, Pulmonary, 3 28 3.914
5
c SRF008 Surfactant Metabolism Dysfunction, Pulmonary, 4 26 3.833
6
c SRF007 Surfactant Metabolism Dysfunction, Pulmonary, 5 21 3.816
7
c SFT007 Sftpc-Related Pulmonary Surfactant Metabolism Dysfunction 9 3.017
8
CSF003 Csfrb-Related Pulmonary Surfactant Metabolism Dysfunction 8 3.017
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 1.894
12
LNG099 Lung Disease 62 0.257
13
PRT011 Protein C Deficiency 51 0.227
14
P PNM007 Pneumonia 66 0.222
15
MCN007 Meconium Aspiration Syndrome 51 0.201
16
c ACT210 Acute Respiratory Distress Syndrome 57 0.201
17
NTR005 Nutritional Deficiency Disease 39 0.201
18
CHL071 Child Syndrome 58 0.200
19
KDS001 Kid Syndrome 53 0.200
20
P ADL010 Adult Respiratory Distress Syndrome 60 0.198
21
P RSP003 Respiratory Failure 70 0.182
22
P THY032 Thyroiditis 54 0.182
23
RSP019 Respiratory Distress Syndrome in Premature Infants 44 0.181
24
PRT014 Protein S Deficiency 52 0.179
25
RSP006 Respiratory System Disease 62 0.177
26
NWB001 Newborn Respiratory Distress Syndrome 47 0.172
27
RSP007 Respiratory Distress Syndrome, Infant 26 0.167
28
CHR322 Choreoathetosis, Hypothyroidism, and Neonatal Respiratory Distress 41 0.162
29
INT066 Interstitial Lung Disease 58 0.159
30
c ADL080 Adult Acute Respiratory Distress Syndrome 23 0.152
31
P PLM006 Pulmonary Alveolar Proteinosis 48 0.152
32
P AST005 Asthma 82 0.152
33
P INF038 Influenza 74 0.151
34
CYS001 Cystic Fibrosis 86 0.145
35
BRN056 Bronchopulmonary Dysplasia 49 0.145
36
ADL002 Adult Syndrome 53 0.143
37
P PLM036 Pulmonary Fibrosis 68 0.141
38
TBR010 Tuberculosis 69 0.140
39
P LNG032 Lung Cancer 94 0.136
40
P HPT021 Hepatitis 70 0.130
41
P ADN016 Adenocarcinoma 69 0.129
42
CRB009 Cerebritis 38 0.128
43
ATH003 Atherosclerosis 62 0.117
44
NNT004 Neonatal Respiratory Failure 41 0.114
45
ALR002 Al-Raqad Syndrome 36 0.114
46
P ART022 Arthritis 75 0.112
47
P LKM002 Leukemia 70 0.108
48
c INH020 Inherited Metabolic Disorder 49 0.107
49
NSD001 Nose Disease 52 0.106
50
DRM006 Dermatitis 61 0.105
51
P OBS005 Obesity 93 0.103
52
PNM008 Pneumothorax 52 0.102
53
END072 Endotheliitis 42 0.101
54
TRC026 Tracheal Disease 35 0.100
55
P RHM011 Rheumatoid Arthritis 88 0.100
56
ACD009 Acid-Labile Subunit, Deficiency of 48 0.097
57
PLM034 Pulmonary Emphysema 54 0.095
58
P NRP001 Neuropathy 60 0.089
59
PLC008 Placenta Disease 36 0.089
60
C3D001 C3 Deficiency 53 0.088
61
P LPS004 Lupus Erythematosus 63 0.088
62
CSY001 C Syndrome 49 0.086
63
P SHR029 Short Syndrome 60 0.084
64
P HRT032 Heart Disease 76 0.083
65
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.083
66
P CNG015 Congenital Diaphragmatic Hernia 58 0.082
67
c SYS001 Systemic Lupus Erythematosus 87 0.082
68
c BLD124 Bleeding Disorder, Platelet-Type, 11 42 0.082
69
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 53 0.082
70
P INF032 Infertility 61 0.082
71
MSS002 Mass Syndrome 59 0.081
72
c PLM150 Pulmonary Alveolar Proteinosis, Acquired 23 0.081
73
c AST037 Asthma 1 31 0.080
74
PCK002 Pick Disease 67 0.080
75
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.080
76
P LYM118 Lymphoma 70 0.080
77
PLM033 Pulmonary Embolism 59 0.079
78
PRV004 Periventricular Leukomalacia 48 0.079
79
PRT056 Protein R Deficiency 14 0.079
80
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 39 0.078
81
ALL026 Allergic Hypersensitivity Disease 53 0.078
82
P PNC044 Pancreatitis 60 0.077
83
BRN002 Bronchiolitis 56 0.077
84
LKM006 Leukomalacia 42 0.077
85
c CNG121 Congenital Pulmonary Alveolar Proteinosis 13 0.077
86
SKN023 Skin Tag 46 0.077
87
HMT018 Hematopoietic Stem Cell Transplantation 41 0.076
88
RTN018 Retinal Disease 56 0.076
89
ISC004 Ischemia 59 0.075
90
P HYP265 Hypotonia 39 0.075
91
LPD004 Lipoid Nephrosis 48 0.074
92
BLD054 Blood Protein Disease 40 0.074
93
c HRD171 Hereditary Pulmonary Alveolar Proteinosis 23 0.073
94
P HYP086 Hypothyroidism 65 0.072
95
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 55 0.072
96
ATP002 Atopy 63 0.072
97
PLM010 Pulmonary Edema 56 0.072
98
c AST039 Asthma 2 31 0.072
99
BRN038 Bronchial Disease 54 0.071
100
ATN011 Autoinflammation with Infantile Enterocolitis 41 0.071
101
P MNN013 Meningitis 65 0.071
102
SKN016 Skin Disease 68 0.071
103
P PLM037 Pulmonary Hypertension 79 0.071
104
ACR041 Acromelic Frontonasal Dysostosis 46 0.071
105
BRT030 Birth Defects 43 0.070
106
PRS047 Prostatitis 56 0.069
107
PRN019 Perinatal Necrotizing Enterocolitis 44 0.069
108
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 56 0.069
109
DMN002 Dementia 64 0.068
110
PLM001 Pulmonary Tuberculosis 68 0.068
111
P ASP006 Aspergillosis 60 0.068
112
CLT003 Colitis 59 0.068
113
CLD014 Cole Disease 39 0.068
114
CHL068 Cholestasis 58 0.067
115
CNT047 Contact Dermatitis 62 0.066
116
SLC006 Silicosis 53 0.066
117
BRN071 Brain Injury 52 0.066
118
IMM136 Immune System Disease 50 0.066
119
GDS001 Good Syndrome 45 0.065
120
WLL006 Wells Syndrome 56 0.064
121
CRN246 Cranioosteoarthropathy 31 0.064
122
P RHN004 Rhinitis 61 0.064
123
LRY017 Laryngeal Disease 37 0.064
124
ALL006 Allergic Asthma 58 0.062
125
P HMN010 Hemangioma 60 0.062
126
P PSR002 Psoriasis 63 0.062
127
CCN007 Cocoon Syndrome 35 0.062
128
c THR092 Thrombophilia Due to Thrombin Defect 56 0.061
129
HYD057 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 44 0.061
130
ART002 Arts Syndrome 53 0.061
131
DRG003 Drug Dependence 53 0.061
132
CHL079 Children's Interstitial Lung Disease 19 0.061
133
OLG003 Oligohydramnios 52 0.061
134
P TRN020 Turner Syndrome 64 0.060
135
VND001 Vein Disease 52 0.060
136
ADJ001 Adjustment Disorder 38 0.058
137
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 49 0.058
138
OTT002 Otitis Media 66 0.058
139
P SPS003 Spastic Diplegia 53 0.058
140
PLM129 Pulmonary Disease, Chronic Obstructive 62 0.058
141
HYP266 Hypoxia 55 0.058
142
P DRR001 Diarrhea 51 0.058
143
PRD011 Proud Syndrome 42 0.057
144
c CRN214 Coronary Heart Disease 5 23 0.057
145
ATN005 Autonomic Dysfunction 45 0.057
146
INT309 Intellectual Developmental Disorder with Persistence of Fetal Hemoglobin 29 0.057
147
ADN018 Adenoma 59 0.057
148
NSY001 N Syndrome 39 0.056
149
CNN005 Connective Tissue Disease 61 0.056
150
VGN023 Vaginitis 42 0.056
151
P ATP001 Atopic Dermatitis 62 0.055
152
VNT001 Ventilation Pneumonitis 37 0.055
153
P ESN008 Eosinophilic Pneumonia 49 0.055
154
STM006 Stomach Disease 50 0.055
155
SKN027 Skin Conditions 45 0.054
156
SCK005 Sickle Cell Disease 49 0.054
157
BRN022 Bronchiectasis 47 0.054
158
WST001 West Syndrome 61 0.053
159
CRB037 Cerebral Palsy 54 0.053
160
ALL010 Allergic Contact Dermatitis 57 0.053
161
PLM012 Pulmonary Sarcoidosis 54 0.053
162
UPP004 Upper Respiratory Tract Disease 48 0.053
163
STC004 Stachybotrys Chartarum 37 0.053
164
P HYP071 Hypersensitivity Reaction Type Ii Disease 51 0.053
165
c HPT001 Hepatitis C 68 0.053
166
P HRP006 Herpes Simplex 65 0.052
167
VCC001 Vaccinia 46 0.052
168
P PRD008 Periodontitis 46 0.052
169
ANG049 Angioedema Induced by Ace Inhibitors 35 0.051
170
ALL003 Allergic Rhinitis 64 0.050
171
BCK006 Back Pain 42 0.050
172
CML001 Cumulative Trauma Disorders 21 0.050
173
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.050
174
P DRM010 Dermatomyositis 58 0.050
175
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 47 0.050
176
MTH009 Mouth Disease 63 0.050
177
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.050
178
HV1006 Hiv-1 82 0.050
179
EYD002 Eye Disease 63 0.050
180
CHL123 Chlamydia 59 0.050
181
P CHR345 Chronic Pain 49 0.050
182
ATN002 Autonomic Nervous System Disease 47 0.050
183
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 47 0.050
184
GLB003 Globe Disease 35 0.050
185
PLR022 Pleural Disease 52 0.049
186
CHR005 Chorioamnionitis 48 0.049
187
P PLM040 Pulmonary Valve Disease 45 0.049
188
c VRL005 Viral Pneumonia 42 0.049
189
SML020 Small Patella Syndrome 36 0.049
190
RBR001 Roberts Syndrome 59 0.049
191
DPH001 Diphtheria 58 0.049
192
P OCY001 Oocyte Maturation Defect 39 0.049
193
c TRC078 Trichohepatoenteric Syndrome 2 31 0.049
194
P LYM026 Lymphoblastic Leukemia 60 0.049
195
c CNG006 Congenital Hypothyroidism 59 0.049
196
ULC004 Ulcerative Colitis 75 0.048
197
DWN001 Down Syndrome 65 0.048
198
GLC008 Glucose Metabolism Disease 47 0.047
199
HYP458 Hyper Ige Syndrome 41 0.047
200
HYD012 Hydrops Fetalis 44 0.047
201
EXT034 Extrinsic Allergic Alveolitis 56 0.047
202
PNM001 Pneumocystosis 50 0.047
203
c CHR096 Chronic Pulmonary Heart Disease 40 0.047
204
BRN012 Bronchiolitis Obliterans 58 0.047
205
c SCN051 Secondary Pulmonary Alveolar Proteinosis 18 0.047
206
P GT001 Gout 58 0.046
207
MLN007 Male Infertility 56 0.046
208
CYT002 Cytokine Deficiency 31 0.046
209
P CRN178 Coronary Heart Disease 6 24 0.046
210
c CRN175 Coronary Heart Disease 4 21 0.046
211
PRP027 Peripheral Vascular Disease 69 0.046
212
VSC007 Vascular Disease 67 0.046
213
GBT001 Gaba-Transaminase Deficiency 27 0.046
214
c CRN173 Coronary Heart Disease 8 20 0.045
215
P ESN007 Eosinophilia 61 0.045
216
HDC001 Headache 54 0.045
217
WLL001 Williams-Beuren Syndrome 61 0.044
218
CRB085 Cerebral Hemorrhage 43 0.044
219
c PLM128 Pulmonary Hypertension, Primary, 2 30 0.044
220
CNT067 Central Cord Syndrome 24 0.044
221
NRM005 Neuromuscular Disease 57 0.044
222
PLS010 Plasma Protein Metabolism Disease 38 0.044
223
ATM012 Autoimmune Disease of Blood 37 0.044
224
LRN003 Learning Disability 51 0.044
225
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 41 0.044
226
STF001 Stiff-Person Syndrome 56 0.043
227
P TMT001 Timothy Syndrome 56 0.043
228
DCB001 Decubitus Ulcer 44 0.043
229
LPD027 Lip Disease 36 0.043
230
c PLM121 Pulmonary Hypertension, Primary, 4 29 0.043
231
GLC037 Glucocorticoid Resistance 62 0.043
232
c HPT003 Hepatitis a 59 0.043
233
CRY005 Cryptococcosis 50 0.043
234
c CRN172 Coronary Heart Disease 3 21 0.043
235
PRM025 Primary Bacterial Infectious Disease 43 0.042
236
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.041
237
P EXN002 Exanthem 57 0.041
238
DBT010 Diabetic Neuropathy 55 0.041
239
P LYM007 Lymphangioleiomyomatosis 65 0.041
240
P ALX003 Alexander Disease 64 0.041
241
SBS003 Substance Abuse 56 0.041
242
P PLY041 Polymyositis 51 0.041
243
c LRG001 Large Cell Carcinoma 51 0.041
244
ACT017 Acute Chest Syndrome 48 0.041
245
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 42 0.041
246
LNS003 Lens Disease 38 0.041
247
ATR003 Atrophic Rhinitis 32 0.041
248
BRW006 Brown Syndrome 26 0.041
249
P PRP019 Peripheral Nervous System Disease 54 0.040
250
BNF002 Bone Fracture 47 0.040
251
CRB031 Cerebral Arterial Disease 31 0.040
252
ATM052 Autoimmune Disease 1 28 0.040
253
BRC012 Brucellosis 65 0.040
254
EXF001 Exfoliation Syndrome 57 0.040
255
CYT008 Cytomegalovirus Infection 51 0.040
256
c SVR001 Severe Acute Respiratory Syndrome 57 0.039
257
PLN006 Poland Syndrome 48 0.039
258
BLL003 Bell's Palsy 46 0.039
259
FCT008 Factitious Disorder 43 0.039
260
HRT012 Heart Valve Disease 41 0.039
261
c PLM127 Pulmonary Hypertension, Primary, 3 30 0.039
262
PLM124 Pulmonary Hypertension, Neonatal 27 0.039
263
WSC001 Wisconsin Syndrome 17 0.039
264
P RTT002 Rett Syndrome 78 0.039
265
PTN001 Patent Foramen Ovale 54 0.039
266
P PLN008 Peeling Skin Syndrome 47 0.039
267
P TCL004 T-Cell Leukemia 46 0.039
268
MSL001 Measles 61 0.038
269
PNC034 Pancreas Disease 57 0.038
270
DMY004 Demyelinating Disease 55 0.038
271
SLV003 Salivary Gland Disease 49 0.038
272
c INV001 Invasive Aspergillosis 47 0.038
273
VSC047 Vascular Malformation 45 0.038
274
P ART084 Arteriovenous Fistula 44 0.038
275
c HYP595 Hypertension, Essential 69 0.037
276
c ACT073 Acute Leukemia 62 0.037
277
TXC005 Toxic Shock Syndrome 61 0.037
278
c ADL017 Adult T-Cell Leukemia 58 0.037
279
LYM019 Lymphosarcoma 53 0.037
280
DRY001 Dry Eye Syndrome 51 0.037
281
ADT003 Auditory System Disease 51 0.037
282
P HRD018 Hair Disease 50 0.037
283
c PLN018 Peeling Skin Syndrome 2 35 0.037
284
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 76 0.036
285
P PLR004 Pleuropulmonary Blastoma 64 0.036
286
P SNS014 Sinusitis 60 0.036
287
P UVT001 Uveitis 59 0.036
288
HMP005 Hemiplegia 54 0.036
289
NRF007 Neurofibroma 52 0.036
290
ASP003 Aseptic Meningitis 51 0.036
291
ADR038 Adermatoglyphia 48 0.036
292
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 35 0.036
293
c DRR009 Diarrhea 6 31 0.036
294
ATM054 Autoimmune Disease 3 18 0.036
295
c KNN009 Kenny-Caffey Syndrome, Type 1 62 0.034
296
LSH001 Leishmaniasis 62 0.034
297
GST092 Gastroesophageal Reflux 61 0.034
298
P MCR129 Microvascular Complications of Diabetes 1 57 0.034
299
GNT003 Genital Herpes 54 0.034
300
P SJG001 Sjogren's Syndrome 53 0.034
301
GNR004 Generalized Anxiety Disorder 51 0.034
302
BRD001 Brody Myopathy 49 0.034
303
LMB062 Limb Ischemia 48 0.034
304
FRM003 Farmer's Lung 47 0.034
305
BHR001 Behr Syndrome 44 0.034
306
GST078 Gastrointestinal Allergy 41 0.034
307
c ADL001 Adult Lymphoma 41 0.034
308
c PNC106 Pancreatic Agenesis 1 40 0.034
309
LCN001 Lice Infestation 32 0.034
310
c AST050 Asthma, Phf11-Related 22 0.034
311
c CRN176 Coronary Heart Disease 9 20 0.034
312
ATM053 Autoimmune Disease 2 19 0.034
313
ATM055 Autoimmune Disease 4 18 0.034
314
P DRV001 Dravet Syndrome 68 0.033
315
BRN024 Bronchitis 63 0.033
316
P SPN301 Spinocerebellar Ataxia 2 63 0.033
317
P VNT002 Ventricular Septal Defect 59 0.033
318
P SYS005 Systemic Scleroderma 58 0.033
319
SLD003 Sialadenitis 48 0.033
320
P OTT001 Otitis Externa 47 0.033
321
P RNL017 Renal Oncocytoma 46 0.033
322
P HMP006 Hemiplegic Migraine 44 0.033
323
P ICH001 Ichthyosis Vulgaris 44 0.033
324
CPL007 Capillary Malformation-Arteriovenous Malformation 41 0.033
325
LCR008 Lacrimal Apparatus Disease 40 0.033
326
LNG013 Lung Lymphoma 40 0.033
327
EXC003 Excessive Tearing 38 0.033
328
ATM059 Autoimmune Disease 6 26 0.033
329
ATM005 Autoimmune Disease of Musculoskeletal System 16 0.033
330
TTR001 Tetralogy of Fallot 71 0.031
331
MLD001 Melioidosis 67 0.031
332
P CNT061 Conotruncal Heart Malformations 62 0.031
333
c FML001 Familial Atrial Fibrillation 59 0.031
334
P EPS003 Episodic Ataxia 56 0.031
335
P ATR001 Atrioventricular Septal Defect 52 0.031
336
P ALT001 Alternating Hemiplegia of Childhood 52 0.031
337
HPT009 Hepatopulmonary Syndrome 48 0.031
338
PLM041 Pulmonary Valve Stenosis 48 0.031
339
ASP007 Aspiration Pneumonia 46 0.031
340
P TRC086 Trichohepatoenteric Syndrome 1 46 0.031
341
BYS001 Byssinosis 31 0.031
342
MN1001 Mn1 31 0.031
343
PRN029 Parainfluenza Virus Type 3 30 0.031
344
ALV006 Alveolar Capillary Dysplasia 30 0.031
345
IMM002 Immature Cataract 28 0.031
346
GMM004 Gamma-Amino Butyric Acid Metabolism Disorder 24 0.031
347
P GNR027 Generalized Peeling Skin Syndrome 22 0.031
348
PLM134 Pulmonary Fibrosis, Idiopathic 61 0.029
349
c FML023 Familial Hemiplegic Migraine 55 0.029
350
CHR177 Chromophobe Renal Cell Carcinoma 53 0.029
351
DBT062 Diabetic Foot Ulcers 52 0.029
352
P PNM006 Pneumoconiosis 51 0.029
353
c RBN018 Robinow Syndrome, Autosomal Dominant 1 48 0.029
354
TRN044 Transposition of the Great Arteries 47 0.029
355
PLM017 Pulmonary Alveolar Microlithiasis 46 0.029
356
IRR003 Irritant Dermatitis 46 0.029
357
DBT008 Diabetic Angiopathy 45 0.029
358
EBS001 Ebstein Anomaly 44 0.029
359
P TRC087 Tricuspid Valve Disease 44 0.029
360
P ATR010 Atrial Heart Septal Defect 43 0.029
361
STT002 Status Asthmaticus 43 0.029
362
ATS008 Autosomal Dominant Disease 42 0.029
363
ASB001 Asbestosis 42 0.029
364
HRT011 Heart Septal Defect 41 0.029
365
c BNG023 Benign Familial Infantile Epilepsy 41 0.029
366
CPL005 Capillary Disease 40 0.029
367
PDT001 Pediatric Lymphoma 40 0.029
368
c ACT004 Acute Diarrhea 38 0.029
369
AMY002 Amyloid Tumor 37 0.029
370
ISC001 Ischemic Neuropathy 33 0.029
371
c DRR007 Diarrhea 7 33 0.029
372
P ACT080 Acute Pulmonary Heart Disease 32 0.029
373
EPT008 Epithelioid Malignant Peripheral Nerve Sheath Tumor 31 0.029
374
c ATM007 Autoimmune Disease of Central Nervous System 28 0.029
375
c MLT094 Multiple Sclerosis 3 26 0.029
376
TNY001 Tanycytic Ependymoma 26 0.029
377
PRM133 Primary Pulmonary Lymphoma 24 0.029
378
VSC009 Vascular Skin Disease 22 0.029
379
c SML023 Small Cell Lung Cancer, Adult 17 0.029