Search results for "surfactant protein c deficiency"

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

374 hits were found for 'surfactant protein c deficiency'

# Family MCID Name MIFTS Score
1
c SRF003 Surfactant Metabolism Dysfunction, Pulmonary, 2 29 6.039
2
c SFT007 Sftpc-Related Pulmonary Surfactant Metabolism Dysfunction 9 3.929
3
P HPT021 Hepatitis 69 0.610
4
c HPT001 Hepatitis C 68 0.483
5
END072 Endotheliitis 42 0.392
6
PRT011 Protein C Deficiency 52 0.357
7
P LKM002 Leukemia 71 0.345
8
P THY032 Thyroiditis 54 0.295
9
P LNG032 Lung Cancer 95 0.293
10
PRS047 Prostatitis 56 0.282
11
P ADN016 Adenocarcinoma 69 0.266
12
THR024 Thrombosis 57 0.265
13
P PNM007 Pneumonia 68 0.258
14
P LYM118 Lymphoma 69 0.256
15
PRT014 Protein S Deficiency 53 0.250
16
P PNC044 Pancreatitis 61 0.249
17
LNG099 Lung Disease 64 0.244
18
HV1006 Hiv-1 80 0.236
19
P ART022 Arthritis 75 0.230
20
CRB009 Cerebritis 39 0.228
21
P INF038 Influenza 72 0.227
22
P OBS005 Obesity 92 0.225
23
P PRS040 Prostate Cancer 90 0.224
24
NTR005 Nutritional Deficiency Disease 36 0.224
25
P AST005 Asthma 82 0.205
26
ATH003 Atherosclerosis 65 0.203
27
SQM006 Squamous Cell Carcinoma 70 0.203
28
P RHM011 Rheumatoid Arthritis 89 0.199
29
CYS001 Cystic Fibrosis 83 0.198
30
TBR010 Tuberculosis 70 0.197
31
c HPT003 Hepatitis a 59 0.190
32
ISC004 Ischemia 61 0.186
33
HYP266 Hypoxia 56 0.179
34
P HRT032 Heart Disease 75 0.178
35
CHL071 Child Syndrome 58 0.175
36
c ACT210 Acute Respiratory Distress Syndrome 57 0.175
37
KDS001 Kid Syndrome 53 0.174
38
P RSP003 Respiratory Failure 71 0.165
39
P LPS004 Lupus Erythematosus 64 0.164
40
P ADL010 Adult Respiratory Distress Syndrome 61 0.163
41
RSP006 Respiratory System Disease 58 0.162
42
P KDN018 Kidney Disease 66 0.161
43
SRF006 Surfactant Dysfunction 33 0.159
44
c SYS001 Systemic Lupus Erythematosus 86 0.157
45
P PLM036 Pulmonary Fibrosis 71 0.156
46
INT066 Interstitial Lung Disease 59 0.151
47
PCK002 Pick Disease 68 0.150
48
BLD054 Blood Protein Disease 37 0.150
49
CSY001 C Syndrome 50 0.149
50
RSP019 Respiratory Distress Syndrome in Premature Infants 43 0.148
51
ADL002 Adult Syndrome 52 0.147
52
MCN007 Meconium Aspiration Syndrome 52 0.145
53
P NRP001 Neuropathy 59 0.144
54
P GLB002 Glioblastoma 68 0.141
55
NWB001 Newborn Respiratory Distress Syndrome 45 0.141
56
ADN018 Adenoma 58 0.138
57
RSP007 Respiratory Distress Syndrome, Infant 22 0.138
58
DRM006 Dermatitis 66 0.136
59
CHR322 Choreoathetosis, Hypothyroidism, and Neonatal Respiratory Distress 40 0.134
60
P PLM006 Pulmonary Alveolar Proteinosis 48 0.133
61
P HRP006 Herpes Simplex 65 0.132
62
DMN002 Dementia 65 0.130
63
c ADL080 Adult Acute Respiratory Distress Syndrome 19 0.128
64
P INF037 Inflammatory Bowel Disease 63 0.127
65
P PRD008 Periodontitis 63 0.127
66
P MNN013 Meningitis 67 0.127
67
P INF032 Infertility 59 0.126
68
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.125
69
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 54 0.124
70
BRN056 Bronchopulmonary Dysplasia 48 0.122
71
ALR002 Al-Raqad Syndrome 36 0.121
72
CLT003 Colitis 60 0.121
73
P PSR002 Psoriasis 61 0.118
74
P TCL004 T-Cell Leukemia 47 0.117
75
ACQ007 Acquired Immunodeficiency Syndrome 60 0.114
76
P THL005 Thalassemia 64 0.114
77
VCC001 Vaccinia 46 0.113
78
c INH020 Inherited Metabolic Disorder 49 0.112
79
P PLM037 Pulmonary Hypertension 79 0.110
80
ALL026 Allergic Hypersensitivity Disease 52 0.110
81
P LYM026 Lymphoblastic Leukemia 62 0.108
82
ACD009 Acid-Labile Subunit, Deficiency of 45 0.107
83
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.105
84
BRN071 Brain Injury 52 0.103
85
MCS002 Mucositis 55 0.103
86
C3D001 C3 Deficiency 53 0.101
87
c HMG001 Hemoglobin C Disease 47 0.100
88
c SVR001 Severe Acute Respiratory Syndrome 57 0.100
89
PLM033 Pulmonary Embolism 60 0.099
90
NNT004 Neonatal Respiratory Failure 37 0.098
91
P BLD124 Bleeding Disorder, Platelet-Type, 11 40 0.098
92
CHL123 Chlamydia 60 0.097
93
c ACT073 Acute Leukemia 60 0.097
94
ULC004 Ulcerative Colitis 76 0.096
95
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.096
96
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.095
97
P HYP086 Hypothyroidism 64 0.095
98
ACR041 Acromelic Frontonasal Dysostosis 45 0.095
99
NSD001 Nose Disease 48 0.095
100
P ATP001 Atopic Dermatitis 62 0.094
101
P DRR001 Diarrhea 60 0.094
102
ATP002 Atopy 66 0.094
103
PLC008 Placenta Disease 33 0.094
104
MTH009 Mouth Disease 61 0.094
105
SKN016 Skin Disease 66 0.093
106
DWN001 Down Syndrome 66 0.093
107
MSL001 Measles 61 0.093
108
BRT030 Birth Defects 43 0.093
109
PLM001 Pulmonary Tuberculosis 67 0.092
110
BRN002 Bronchiolitis 56 0.092
111
SKN023 Skin Tag 44 0.092
112
HMT018 Hematopoietic Stem Cell Transplantation 41 0.091
113
VSC007 Vascular Disease 67 0.091
114
STM006 Stomach Disease 50 0.090
115
P RHN004 Rhinitis 60 0.090
116
CHL068 Cholestasis 59 0.090
117
P SPS003 Spastic Diplegia 52 0.089
118
WLL006 Wells Syndrome 59 0.089
119
IMM136 Immune System Disease 51 0.088
120
ADJ001 Adjustment Disorder 38 0.088
121
CNN005 Connective Tissue Disease 62 0.087
122
GLC008 Glucose Metabolism Disease 42 0.087
123
BRN038 Bronchial Disease 51 0.087
124
GDS001 Good Syndrome 44 0.087
125
LPD004 Lipoid Nephrosis 48 0.086
126
DPH001 Diphtheria 59 0.086
127
MSS002 Mass Syndrome 48 0.085
128
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.085
129
c SRF005 Surfactant Metabolism Dysfunction, Pulmonary, 3 28 0.084
130
TRC026 Tracheal Disease 35 0.084
131
PLM034 Pulmonary Emphysema 55 0.084
132
P ALX003 Alexander Disease 63 0.083
133
PRM025 Primary Bacterial Infectious Disease 41 0.083
134
TTH006 Tooth Disease 52 0.082
135
PRT056 Protein R Deficiency 10 0.082
136
P SHR029 Short Syndrome 58 0.082
137
ALL006 Allergic Asthma 58 0.082
138
c AST037 Asthma 1 29 0.081
139
P RTT002 Rett Syndrome 77 0.081
140
VND001 Vein Disease 47 0.080
141
P HYP071 Hypersensitivity Reaction Type Ii Disease 49 0.080
142
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 57 0.080
143
P PLY019 Polyneuropathy 56 0.080
144
SCK005 Sickle Cell Disease 51 0.079
145
PRP027 Peripheral Vascular Disease 69 0.079
146
RTN018 Retinal Disease 53 0.079
147
PLS010 Plasma Protein Metabolism Disease 34 0.079
148
NRM005 Neuromuscular Disease 56 0.079
149
ALL003 Allergic Rhinitis 63 0.077
150
PLM066 Pulmonary Surfactant Protein B, Deficiency of 5 0.077
151
CNT047 Contact Dermatitis 61 0.076
152
P CHR071 Charcot-Marie-Tooth Disease 67 0.075
153
c AST039 Asthma 2 28 0.074
154
PLM010 Pulmonary Edema 54 0.074
155
WST001 West Syndrome 57 0.074
156
c CRN214 Coronary Heart Disease 5 22 0.074
157
EYD002 Eye Disease 61 0.074
158
LSH001 Leishmaniasis 66 0.073
159
c TRC078 Trichohepatoenteric Syndrome 2 29 0.073
160
OTT002 Otitis Media 66 0.073
161
MLN007 Male Infertility 55 0.073
162
LYM019 Lymphosarcoma 53 0.072
163
SCK003 Sickle Cell Anemia 71 0.072
164
GLB003 Globe Disease 32 0.072
165
P CNG015 Congenital Diaphragmatic Hernia 60 0.070
166
c THR092 Thrombophilia Due to Thrombin Defect 54 0.070
167
VGN023 Vaginitis 42 0.070
168
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.070
169
ART002 Arts Syndrome 51 0.070
170
CHR005 Chorioamnionitis 48 0.070
171
P ASP006 Aspergillosis 61 0.070
172
ATN011 Autoinflammation with Infantile Enterocolitis 39 0.069
173
DRG003 Drug Dependence 50 0.069
174
TXC005 Toxic Shock Syndrome 60 0.069
175
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.069
176
P TBR001 Tuberous Sclerosis 67 0.068
177
CYT008 Cytomegalovirus Infection 52 0.068
178
NSY001 N Syndrome 36 0.068
179
P RNL017 Renal Oncocytoma 47 0.068
180
PRP019 Peripheral Nervous System Disease 55 0.068
181
P HMN010 Hemangioma 59 0.068
182
BLM001 Bloom Syndrome 63 0.068
183
P UVT001 Uveitis 58 0.067
184
PNC034 Pancreas Disease 58 0.067
185
c CRN175 Coronary Heart Disease 4 19 0.067
186
SKN027 Skin Conditions 43 0.066
187
PRV004 Periventricular Leukomalacia 48 0.066
188
BRC012 Brucellosis 66 0.066
189
MLD001 Melioidosis 67 0.066
190
PLM129 Pulmonary Disease, Chronic Obstructive 63 0.066
191
CRB085 Cerebral Hemorrhage 46 0.065
192
c PNC106 Pancreatic Agenesis 1 37 0.065
193
CHR177 Chromophobe Renal Cell Carcinoma 56 0.065
194
P EXN002 Exanthem 57 0.065
195
c CRN172 Coronary Heart Disease 3 19 0.064
196
c ADL017 Adult T-Cell Leukemia 60 0.064
197
PRN029 Parainfluenza Virus Type 3 31 0.064
198
P CHR345 Chronic Pain 50 0.064
199
SLC006 Silicosis 53 0.064
200
BNF002 Bone Fracture 50 0.064
201
P ICH004 Ichthyosis 52 0.064
202
BRN024 Bronchitis 64 0.064
203
ATM052 Autoimmune Disease 1 25 0.063
204
ANG049 Angioedema Induced by Ace Inhibitors 34 0.063
205
CLD014 Cole Disease 37 0.063
206
PLM012 Pulmonary Sarcoidosis 54 0.063
207
LRN003 Learning Disability 49 0.063
208
P PLZ001 Pelizaeus-Merzbacher Disease 65 0.062
209
ATN002 Autonomic Nervous System Disease 48 0.062
210
ATN005 Autonomic Dysfunction 49 0.062
211
c ADL001 Adult Lymphoma 39 0.062
212
LRY017 Laryngeal Disease 34 0.062
213
UPP004 Upper Respiratory Tract Disease 46 0.062
214
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 36 0.061
215
CCN007 Cocoon Syndrome 45 0.061
216
P GT001 Gout 58 0.061
217
P DRM010 Dermatomyositis 62 0.061
218
DBT010 Diabetic Neuropathy 55 0.061
219
NRT004 Neuritis 52 0.060
220
P CRN178 Coronary Heart Disease 6 21 0.060
221
PRD011 Proud Syndrome 42 0.060
222
P LNG064 Lung Cancer Susceptibility 3 62 0.060
223
c CNT068 Central Pain Syndrome 29 0.060
224
ATM053 Autoimmune Disease 2 16 0.059
225
c HYP595 Hypertension, Essential 69 0.059
226
RBR001 Roberts Syndrome 60 0.059
227
BRN012 Bronchiolitis Obliterans 58 0.059
228
BRN022 Bronchiectasis 50 0.059
229
CRB037 Cerebral Palsy 66 0.059
230
P PLY041 Polymyositis 52 0.059
231
P ESN008 Eosinophilic Pneumonia 51 0.058
232
HMG005 Hemoglobinopathy 52 0.058
233
SBS003 Substance Abuse 54 0.058
234
c CRN173 Coronary Heart Disease 8 18 0.058
235
P TRN020 Turner Syndrome 65 0.058
236
ATM012 Autoimmune Disease of Blood 35 0.058
237
VSC047 Vascular Malformation 45 0.057
238
HYP711 Hypotonia, Ataxia, and Delayed Development Syndrome 26 0.057
239
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.056
240
P MCR129 Microvascular Complications of Diabetes 1 54 0.056
241
STC004 Stachybotrys Chartarum 37 0.056
242
P SNS014 Sinusitis 60 0.056
243
ATM054 Autoimmune Disease 3 15 0.055
244
THL018 Thalassemia Major 48 0.055
245
ALL010 Allergic Contact Dermatitis 57 0.055
246
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.055
247
EXF001 Exfoliation Syndrome 57 0.055
248
CRN246 Cranioosteoarthropathy 31 0.054
249
c VRL005 Viral Pneumonia 42 0.054
250
CYT002 Cytokine Deficiency 30 0.054
251
BCK006 Back Pain 43 0.054
252
GST078 Gastrointestinal Allergy 40 0.054
253
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 60 0.054
254
c LRG001 Large Cell Carcinoma 51 0.053
255
P AXN001 Axonal Neuropathy 38 0.053
256
P OCY001 Oocyte Maturation Defect 38 0.052
257
IDP011 Idiopathic Interstitial Pneumonia 56 0.052
258
OLV001 Olivopontocerebellar Atrophy 53 0.052
259
P PLN008 Peeling Skin Syndrome 45 0.052
260
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.051
261
VNT001 Ventilation Pneumonitis 35 0.051
262
c CNG027 Congenital Hemolytic Anemia 48 0.051
263
WLL001 Williams-Beuren Syndrome 60 0.051
264
c CHR096 Chronic Pulmonary Heart Disease 40 0.051
265
THL010 Thalassemia Minor 39 0.051
266
CHL079 Children's Interstitial Lung Disease 18 0.050
267
GLC037 Glucocorticoid Resistance 62 0.050
268
CRB031 Cerebral Arterial Disease 27 0.050
269
NNS002 Nonspecific Interstitial Pneumonia 45 0.050
270
ATM055 Autoimmune Disease 4 15 0.050
271
GNR004 Generalized Anxiety Disorder 51 0.050
272
CRY005 Cryptococcosis 50 0.050
273
ACT017 Acute Chest Syndrome 48 0.049
274
c CNG006 Congenital Hypothyroidism 60 0.049
275
P TRC086 Trichohepatoenteric Syndrome 1 48 0.049
276
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 78 0.049
277
c PLM128 Pulmonary Hypertension, Primary, 2 28 0.049
278
AVN001 Avian Influenza 54 0.048
279
ART005 Arteriovenous Malformation 66 0.048
280
c HMG003 Hemoglobin E Disease 44 0.048
281
c PLN018 Peeling Skin Syndrome 2 40 0.048
282
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 0.047
283
PLR022 Pleural Disease 51 0.047
284
c EHL032 Ehlers-Danlos Syndrome, Type Viib 49 0.046
285
c CRN176 Coronary Heart Disease 9 18 0.046
286
P ART084 Arteriovenous Fistula 44 0.046
287
DMY004 Demyelinating Disease 53 0.046
288
EXT034 Extrinsic Allergic Alveolitis 55 0.046
289
P LYM007 Lymphangioleiomyomatosis 66 0.045
290
CPL007 Capillary Malformation-Arteriovenous Malformation 40 0.045
291
c SML023 Small Cell Lung Cancer, Adult 15 0.045
292
PLN006 Poland Syndrome 54 0.045
293
WSC001 Wisconsin Syndrome 14 0.045
294
ADT003 Auditory System Disease 40 0.045
295
FCT008 Factitious Disorder 41 0.044
296
SML020 Small Patella Syndrome 36 0.044
297
P HRD018 Hair Disease 51 0.044
298
SCL017 Sclerosing Hemangioma 41 0.044
299
TYP027 Type 1 Diabetes Mellitus 10 27 0.044
300
P SJG001 Sjogren's Syndrome 50 0.044
301
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 40 0.044
302
ATM059 Autoimmune Disease 6 22 0.044
303
ADR038 Adermatoglyphia 46 0.043
304
SLD003 Sialadenitis 49 0.043
305
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.043
306
HYP458 Hyper Ige Syndrome 42 0.043
307
P ACT080 Acute Pulmonary Heart Disease 31 0.043
308
LMB062 Limb Ischemia 48 0.043
309
BRW006 Brown Syndrome 29 0.043
310
LNS003 Lens Disease 33 0.043
311
GST092 Gastroesophageal Reflux 62 0.042
312
c CHR527 Charcot-Marie-Tooth Disease, Type 1b 49 0.042
313
P CHR102 Charcot-Marie-Tooth Neuropathy 41 0.042
314
c MLG077 Malignant Peripheral Nerve Sheath Tumor 56 0.042
315
GNT003 Genital Herpes 53 0.042
316
ALT002 Aleutian Mink Disease 33 0.041
317
c PLM127 Pulmonary Hypertension, Primary, 3 28 0.041
318
HRT012 Heart Valve Disease 40 0.041
319
THL017 Thalassemia Intermedia 40 0.041
320
GLS018 Glass Syndrome 34 0.041
321
c INV001 Invasive Aspergillosis 47 0.040
322
SLV003 Salivary Gland Disease 47 0.040
323
DCB001 Decubitus Ulcer 41 0.040
324
BLL003 Bell's Palsy 48 0.040
325
DBT008 Diabetic Angiopathy 44 0.040
326
PLM124 Pulmonary Hypertension, Neonatal 22 0.040
327
PLM134 Pulmonary Fibrosis, Idiopathic 61 0.040
328
LPD027 Lip Disease 28 0.040
329
P GNR027 Generalized Peeling Skin Syndrome 19 0.039
330
P TMT001 Timothy Syndrome 55 0.039
331
SNS003 Sensory Peripheral Neuropathy 45 0.039
332
HRT015 Heritable Pulmonary Arterial Hypertension 45 0.039
333
c DRR009 Diarrhea 6 29 0.039
334
VSC009 Vascular Skin Disease 19 0.039
335
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 37 0.039
336
P PLM040 Pulmonary Valve Disease 43 0.039
337
STF001 Stiff-Person Syndrome 56 0.039
338
c HRD088 Hereditary Neuropathies 40 0.038
339
c ATM007 Autoimmune Disease of Central Nervous System 25 0.038
340
c DRR007 Diarrhea 7 31 0.038
341
ASP003 Aseptic Meningitis 51 0.038
342
GLL022 Guillain-Barre Syndrome 56 0.037
343
PLM018 Pulmonary Sclerosing Hemangioma 39 0.037
344
THL016 Thalassemias, Alpha- 53 0.037
345
c CHR536 Charcot-Marie-Tooth Disease, Type 1a 58 0.037
346
WBR001 Weber Syndrome 41 0.037
347
DJR004 Dejerine-Sottas Disease 46 0.036
348
BRD001 Brody Myopathy 47 0.036
349
EXC003 Excessive Tearing 36 0.036
350
c ACT004 Acute Diarrhea 39 0.036
351
c DBT054 Diabetes Mellitus, Insulin-Dependent, 24 34 0.036
352
LNG013 Lung Lymphoma 38 0.036
353
LCR008 Lacrimal Apparatus Disease 37 0.036
354
c STR092 Striatal Degeneration, Autosomal Dominant 2 27 0.036
355
RSS002 Roussy-Levy Syndrome 50 0.036
356
P PNM006 Pneumoconiosis 51 0.035
357
P SYS005 Systemic Scleroderma 61 0.035
358
FRM003 Farmer's Lung 47 0.035
359
c CHR532 Charcot-Marie-Tooth Disease, Type 2e 49 0.035
360
HPT009 Hepatopulmonary Syndrome 48 0.035
361
BHR001 Behr Syndrome 42 0.035
362
FTD001 Foot Drop 33 0.034
363
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 46 0.034
364
c DBT048 Diabetes Mellitus, Insulin-Dependent, 11 36 0.033
365
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 33 0.033
366
c DBT058 Diabetes Mellitus, Insulin-Dependent, 7 35 0.033
367
c MNN043 Meningioma, Familial 59 0.032
368
RHB002 Rhabdoid Meningioma 36 0.032
369
HNZ001 Heinz Body Anemia 39 0.032
370
P ICH001 Ichthyosis Vulgaris 46 0.032
371
PRM133 Primary Pulmonary Lymphoma 23 0.030
372
MTR007 Motor Peripheral Neuropathy 37 0.030
373
c NRV012 Nervous System Benign Neoplasm 31 0.029
374
NRL005 Neurilemmoma 51 0.029