Search results for "surfactant deficiency"

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

299 hits were found for 'surfactant deficiency'

# Family MCID Name MIFTS Score
1
c SRF003 Surfactant Metabolism Dysfunction, Pulmonary, 2 30 5.051
2
c SRF004 Surfactant Metabolism Dysfunction, Pulmonary, 1 29 4.716
3
SRF006 Surfactant Dysfunction 32 4.133
4
c SRF005 Surfactant Metabolism Dysfunction, Pulmonary, 3 29 3.663
5
c SRF008 Surfactant Metabolism Dysfunction, Pulmonary, 4 27 3.582
6
c SRF007 Surfactant Metabolism Dysfunction, Pulmonary, 5 22 3.540
7
c SFT007 Sftpc-Related Pulmonary Surfactant Metabolism Dysfunction 10 3.083
8
c SFT005 Sftpb-Related Pulmonary Surfactant Metabolism Dysfunction 10 2.963
9
c ABC006 Abca3-Related Pulmonary Surfactant Metabolism Dysfunction 10 2.488
10
PLM066 Pulmonary Surfactant Protein B, Deficiency of 2 1.897
11
LNG099 Lung Disease 63 0.297
12
P PNM007 Pneumonia 67 0.245
13
PRT011 Protein C Deficiency 52 0.229
14
MCN007 Meconium Aspiration Syndrome 52 0.223
15
P ADL010 Adult Respiratory Distress Syndrome 60 0.216
16
c ACT210 Acute Respiratory Distress Syndrome 55 0.215
17
CHL071 Child Syndrome 58 0.204
18
KDS001 Kid Syndrome 53 0.204
19
P RSP003 Respiratory Failure 68 0.199
20
P THY032 Thyroiditis 57 0.197
21
RSP006 Respiratory System Disease 61 0.196
22
RSP019 Respiratory Distress Syndrome in Premature Infants 43 0.190
23
INT066 Interstitial Lung Disease 60 0.187
24
P PLM006 Pulmonary Alveolar Proteinosis 46 0.183
25
NWB001 Newborn Respiratory Distress Syndrome 47 0.180
26
NTR005 Nutritional Deficiency Disease 51 0.178
27
RSP007 Respiratory Distress Syndrome, Infant 26 0.175
28
CHR322 Choreoathetosis, Hypothyroidism, and Neonatal Respiratory Distress 43 0.169
29
ALR002 Al-Raqad Syndrome 36 0.167
30
P INF038 Influenza 71 0.165
31
P AST005 Asthma 80 0.162
32
BRN056 Bronchopulmonary Dysplasia 56 0.161
33
c ADL080 Adult Acute Respiratory Distress Syndrome 21 0.158
34
ADL002 Adult Syndrome 53 0.154
35
CYS001 Cystic Fibrosis 87 0.154
36
TBR010 Tuberculosis 70 0.153
37
P PLM036 Pulmonary Fibrosis 69 0.152
38
PRT014 Protein S Deficiency 54 0.150
39
P LNG032 Lung Cancer 92 0.145
40
P ADN016 Adenocarcinoma 69 0.141
41
CRB009 Cerebritis 36 0.137
42
P HPT021 Hepatitis 74 0.137
43
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.126
44
NNT004 Neonatal Respiratory Failure 38 0.117
45
P ART022 Arthritis 73 0.116
46
c BLD124 Bleeding Disorder, Platelet-Type, 11 37 0.115
47
ATH003 Atherosclerosis 63 0.115
48
c CNG121 Congenital Pulmonary Alveolar Proteinosis 14 0.113
49
NSD001 Nose Disease 51 0.112
50
P OBS005 Obesity 91 0.110
51
PNM008 Pneumothorax 51 0.109
52
P LKM002 Leukemia 70 0.109
53
END072 Endotheliitis 41 0.106
54
P RHM011 Rheumatoid Arthritis 87 0.104
55
DRM006 Dermatitis 58 0.104
56
P HYP265 Hypotonia 39 0.104
57
c PLM150 Pulmonary Alveolar Proteinosis, Acquired 22 0.103
58
P CNG015 Congenital Diaphragmatic Hernia 58 0.099
59
c CNG401 Congenital Heart Disease 67 0.096
60
PLC008 Placenta Disease 33 0.096
61
TRC026 Tracheal Disease 33 0.094
62
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 52 0.094
63
PLM034 Pulmonary Emphysema 55 0.093
64
P HRT032 Heart Disease 64 0.093
65
CRN246 Cranioosteoarthropathy 32 0.093
66
ACD009 Acid-Labile Subunit, Deficiency of 37 0.093
67
P LPS004 Lupus Erythematosus 63 0.092
68
BRN002 Bronchiolitis 56 0.091
69
P SHR029 Short Syndrome 60 0.087
70
c SYS001 Systemic Lupus Erythematosus 87 0.087
71
PLM001 Pulmonary Tuberculosis 69 0.084
72
P PNC044 Pancreatitis 62 0.083
73
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 30 0.083
74
PRV004 Periventricular Leukomalacia 51 0.083
75
RTN018 Retinal Disease 55 0.083
76
c INH020 Inherited Metabolic Disorder 49 0.081
77
C3D001 C3 Deficiency 50 0.080
78
P INF032 Infertility 61 0.080
79
LKM006 Leukomalacia 41 0.079
80
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 57 0.079
81
PLM033 Pulmonary Embolism 59 0.079
82
P MNN013 Meningitis 66 0.079
83
PLM010 Pulmonary Edema 56 0.078
84
P HYP086 Hypothyroidism 63 0.078
85
P ASP006 Aspergillosis 61 0.077
86
P KDN018 Kidney Disease 64 0.077
87
SLC006 Silicosis 53 0.075
88
PRN019 Perinatal Necrotizing Enterocolitis 47 0.075
89
SML020 Small Patella Syndrome 36 0.075
90
PCK002 Pick Disease 66 0.074
91
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 38 0.073
92
PRS047 Prostatitis 56 0.073
93
P PLM037 Pulmonary Hypertension 78 0.073
94
HMT018 Hematopoietic Stem Cell Transplantation 39 0.073
95
ATN011 Autoinflammation with Infantile Enterocolitis 36 0.072
96
CLT003 Colitis 56 0.071
97
c AST037 Asthma 1 35 0.071
98
SKN023 Skin Tag 48 0.071
99
DMN002 Dementia 62 0.071
100
P HMN010 Hemangioma 62 0.069
101
P RHN004 Rhinitis 59 0.069
102
P PSR002 Psoriasis 63 0.068
103
BLD054 Blood Protein Disease 38 0.067
104
CSY001 C Syndrome 49 0.067
105
ACQ007 Acquired Immunodeficiency Syndrome 60 0.067
106
OTT002 Otitis Media 66 0.067
107
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 41 0.067
108
OLG003 Oligohydramnios 52 0.066
109
PTN002 Patent Ductus Arteriosus 50 0.066
110
EYD002 Eye Disease 62 0.066
111
LPD004 Lipoid Nephrosis 49 0.065
112
ALL026 Allergic Hypersensitivity Disease 53 0.065
113
P HRM001 Hermansky-Pudlak Syndrome 56 0.064
114
STF001 Stiff-Person Syndrome 54 0.064
115
LRY017 Laryngeal Disease 33 0.064
116
SCK005 Sickle Cell Disease 51 0.063
117
c THR092 Thrombophilia Due to Thrombin Defect 56 0.062
118
HDC001 Headache 52 0.062
119
P TRN020 Turner Syndrome 64 0.062
120
ISC004 Ischemia 56 0.062
121
HYP266 Hypoxia 55 0.062
122
c AST039 Asthma 2 28 0.061
123
VGN023 Vaginitis 41 0.061
124
ADN018 Adenoma 59 0.061
125
CNT047 Contact Dermatitis 62 0.061
126
GDS001 Good Syndrome 46 0.061
127
PLM012 Pulmonary Sarcoidosis 54 0.060
128
P ESN008 Eosinophilic Pneumonia 47 0.060
129
DRG003 Drug Dependence 53 0.060
130
CHL079 Children's Interstitial Lung Disease 18 0.060
131
STC004 Stachybotrys Chartarum 38 0.060
132
P ATP001 Atopic Dermatitis 60 0.060
133
WLL006 Wells Syndrome 57 0.060
134
P CRN178 Coronary Heart Disease 6 22 0.060
135
BRN071 Brain Injury 51 0.059
136
BRN038 Bronchial Disease 54 0.059
137
CCN007 Cocoon Syndrome 32 0.059
138
P DRM010 Dermatomyositis 59 0.059
139
GBT001 Gaba-Transaminase Deficiency 28 0.059
140
SKN016 Skin Disease 69 0.059
141
CHR005 Chorioamnionitis 47 0.058
142
P DGR001 Digeorge Syndrome 52 0.058
143
EXT034 Extrinsic Allergic Alveolitis 58 0.058
144
ATP002 Atopy 62 0.056
145
CHL123 Chlamydia 60 0.056
146
P PRD008 Periodontitis 46 0.056
147
VND001 Vein Disease 51 0.056
148
BRN022 Bronchiectasis 55 0.056
149
PNM001 Pneumocystosis 50 0.056
150
PTN001 Patent Foramen Ovale 55 0.056
151
ATN005 Autonomic Dysfunction 44 0.056
152
c HPT001 Hepatitis C 68 0.056
153
ALL003 Allergic Rhinitis 67 0.054
154
P LYM007 Lymphangioleiomyomatosis 65 0.054
155
P LNG064 Lung Cancer Susceptibility 3 62 0.054
156
P PLM040 Pulmonary Valve Disease 45 0.054
157
BRN012 Bronchiolitis Obliterans 58 0.054
158
UPP004 Upper Respiratory Tract Disease 48 0.054
159
VCC001 Vaccinia 46 0.054
160
c CNG006 Congenital Hypothyroidism 59 0.054
161
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 36 0.053
162
P SPS003 Spastic Diplegia 49 0.053
163
c AST050 Asthma, Phf11-Related 23 0.053
164
ACR041 Acromelic Frontonasal Dysostosis 45 0.053
165
P LYM026 Lymphoblastic Leukemia 60 0.053
166
BRT030 Birth Defects 44 0.053
167
c VRL005 Viral Pneumonia 44 0.053
168
ALL010 Allergic Contact Dermatitis 58 0.052
169
P NRV006 Nervous System Cancer 62 0.052
170
NSY001 N Syndrome 42 0.052
171
DPH001 Diphtheria 55 0.052
172
ULC004 Ulcerative Colitis 74 0.052
173
P HYP071 Hypersensitivity Reaction Type Ii Disease 46 0.052
174
ADJ001 Adjustment Disorder 38 0.051
175
PRT056 Protein R Deficiency 12 0.051
176
c SCN051 Secondary Pulmonary Alveolar Proteinosis 15 0.051
177
HYD012 Hydrops Fetalis 45 0.051
178
CRB037 Cerebral Palsy 54 0.050
179
PLM129 Pulmonary Disease, Chronic Obstructive 61 0.050
180
P ESN007 Eosinophilia 61 0.050
181
CRY005 Cryptococcosis 50 0.050
182
P CNT061 Conotruncal Heart Malformations 61 0.050
183
HMP005 Hemiplegia 52 0.050
184
PRD011 Proud Syndrome 42 0.049
185
c CRN214 Coronary Heart Disease 5 22 0.049
186
P DRV001 Dravet Syndrome 66 0.049
187
P VNT002 Ventricular Septal Defect 59 0.049
188
c LRG001 Large Cell Carcinoma 49 0.049
189
P HMP006 Hemiplegic Migraine 45 0.049
190
GMM004 Gamma-Amino Butyric Acid Metabolism Disorder 23 0.049
191
TTR001 Tetralogy of Fallot 69 0.047
192
NRF007 Neurofibroma 53 0.047
193
IMM002 Immature Cataract 28 0.047
194
P SML002 Small Cell Sarcoma 39 0.047
195
BCK006 Back Pain 40 0.047
196
AMY002 Amyloid Tumor 37 0.047
197
WST001 West Syndrome 61 0.047
198
STM006 Stomach Disease 48 0.047
199
HV1006 Hiv-1 80 0.046
200
P VLC001 Velocardiofacial Syndrome 64 0.046
201
P EPS003 Episodic Ataxia 58 0.046
202
c FML001 Familial Atrial Fibrillation 59 0.046
203
CLD014 Cole Disease 38 0.046
204
P ATR001 Atrioventricular Septal Defect 52 0.046
205
PLM041 Pulmonary Valve Stenosis 48 0.046
206
ALL006 Allergic Asthma 59 0.046
207
P PLY041 Polymyositis 49 0.046
208
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 60 0.046
209
c HPT003 Hepatitis a 55 0.046
210
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 45 0.045
211
TXC005 Toxic Shock Syndrome 61 0.045
212
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 42 0.045
213
CYT008 Cytomegalovirus Infection 51 0.045
214
VNT001 Ventilation Pneumonitis 35 0.045
215
GLB003 Globe Disease 34 0.045
216
P ALT001 Alternating Hemiplegia of Childhood 52 0.044
217
EBS001 Ebstein Anomaly 44 0.044
218
c BNG023 Benign Familial Infantile Epilepsy 40 0.044
219
P ATR010 Atrial Heart Septal Defect 41 0.044
220
TRN044 Transposition of the Great Arteries 48 0.044
221
ATR003 Atrophic Rhinitis 30 0.044
222
HRT011 Heart Septal Defect 40 0.044
223
EPT008 Epithelioid Malignant Peripheral Nerve Sheath Tumor 31 0.044
224
TNY001 Tanycytic Ependymoma 28 0.044
225
ATS008 Autosomal Dominant Disease 41 0.044
226
SNG009 Single Ventricular Septal Defect 28 0.044
227
RBR001 Roberts Syndrome 61 0.043
228
PRP019 Peripheral Nervous System Disease 52 0.043
229
LSH001 Leishmaniasis 63 0.043
230
P SNS014 Sinusitis 66 0.043
231
ANG049 Angioedema Induced by Ace Inhibitors 35 0.043
232
ETH011 Ethylmalonic Encephalopathy 57 0.043
233
P TBR001 Tuberous Sclerosis 68 0.043
234
OCY001 Oocyte Maturation Defect 31 0.043
235
c ADL017 Adult T-Cell Leukemia 59 0.043
236
SKN027 Skin Conditions 44 0.043
237
ASP003 Aseptic Meningitis 51 0.043
238
P TCL004 T-Cell Leukemia 44 0.043
239
BNF002 Bone Fracture 46 0.043
240
c FML023 Familial Hemiplegic Migraine 55 0.042
241
c MLG077 Malignant Peripheral Nerve Sheath Tumor 56 0.042
242
ATN002 Autonomic Nervous System Disease 46 0.042
243
P UVT001 Uveitis 60 0.042
244
P RTT002 Rett Syndrome 77 0.041
245
DWN001 Down Syndrome 65 0.041
246
MSL001 Measles 61 0.041
247
c TRC078 Trichohepatoenteric Syndrome 2 30 0.041
248
c INV001 Invasive Aspergillosis 44 0.041
249
FRM003 Farmer's Lung 47 0.040
250
c CHR096 Chronic Pulmonary Heart Disease 40 0.040
251
P ART084 Arteriovenous Fistula 40 0.040
252
BRN024 Bronchitis 67 0.039
253
WLL001 Williams-Beuren Syndrome 61 0.039
254
c CRN173 Coronary Heart Disease 8 19 0.038
255
MVD001 Moved to 60 0.037
256
P TMT001 Timothy Syndrome 58 0.037
257
P SYS005 Systemic Scleroderma 60 0.037
258
GNT003 Genital Herpes 55 0.037
259
DCB001 Decubitus Ulcer 44 0.037
260
PLM017 Pulmonary Alveolar Microlithiasis 46 0.037
261
c PLM128 Pulmonary Hypertension, Primary, 2 36 0.037
262
LNS003 Lens Disease 37 0.037
263
LPD027 Lip Disease 35 0.037
264
BYS001 Byssinosis 32 0.037
265
CRB085 Cerebral Hemorrhage 40 0.037
266
CNT067 Central Cord Syndrome 22 0.037
267
ART002 Arts Syndrome 53 0.035
268
P ALX003 Alexander Disease 64 0.035
269
P ICH001 Ichthyosis Vulgaris 44 0.035
270
MLD001 Melioidosis 67 0.035
271
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 42 0.035
272
MSS002 Mass Syndrome 49 0.035
273
CRV047 Cervical Cancer, Somatic 65 0.035
274
P RNL017 Renal Oncocytoma 48 0.035
275
ACT017 Acute Chest Syndrome 50 0.035
276
BRW006 Brown Syndrome 31 0.035
277
HPT009 Hepatopulmonary Syndrome 48 0.035
278
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.034
279
MCH010 Michels Syndrome 24 0.034
280
ALV006 Alveolar Capillary Dysplasia 32 0.034
281
P PNM006 Pneumoconiosis 51 0.034
282
PRN029 Parainfluenza Virus Type 3 34 0.034
283
MN1001 Mn1 28 0.034
284
PLM134 Pulmonary Fibrosis, Idiopathic 61 0.031
285
BLL003 Bell's Palsy 47 0.031
286
P IGN003 Iga Nephropathy 1 31 0.031
287
PLN006 Poland Syndrome 48 0.031
288
c PLM127 Pulmonary Hypertension, Primary, 3 31 0.031
289
PLM124 Pulmonary Hypertension, Neonatal 25 0.031
290
c SVR001 Severe Acute Respiratory Syndrome 56 0.031
291
IRR003 Irritant Dermatitis 45 0.031
292
STT002 Status Asthmaticus 43 0.031
293
SLD003 Sialadenitis 45 0.031
294
DSQ001 Desquamative Interstitial Pneumonia 33 0.031
295
ASB001 Asbestosis 42 0.031
296
CHR177 Chromophobe Renal Cell Carcinoma 43 0.031
297
FCT008 Factitious Disorder 42 0.031
298
HRT012 Heart Valve Disease 39 0.031
299
WSC001 Wisconsin Syndrome 16 0.031