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"

243 hits were found for 'surfactant protein c deficiency'

# Family MCID Name MIFTS Score
1
c SRF003 Surfactant Metabolism Dysfunction, Pulmonary, 2 30 5.950
2
c SFT007 Sftpc-Related Pulmonary Surfactant Metabolism Dysfunction 10 3.981
3
P HPT021 Hepatitis 74 0.664
4
c HPT001 Hepatitis C 68 0.516
5
END072 Endotheliitis 41 0.439
6
PRT011 Protein C Deficiency 52 0.392
7
P LKM002 Leukemia 70 0.385
8
P THY032 Thyroiditis 57 0.335
9
P LNG032 Lung Cancer 92 0.326
10
PRS047 Prostatitis 56 0.304
11
P ADN016 Adenocarcinoma 69 0.299
12
P PNM007 Pneumonia 67 0.294
13
LNG099 Lung Disease 63 0.288
14
P PNC044 Pancreatitis 62 0.282
15
HV1006 Hiv-1 80 0.275
16
P INF038 Influenza 71 0.267
17
P OBS005 Obesity 91 0.267
18
CRB009 Cerebritis 36 0.260
19
PRT014 Protein S Deficiency 54 0.257
20
P ART022 Arthritis 73 0.256
21
P RHM011 Rheumatoid Arthritis 87 0.230
22
P AST005 Asthma 80 0.229
23
NTR005 Nutritional Deficiency Disease 51 0.225
24
CYS001 Cystic Fibrosis 87 0.222
25
TBR010 Tuberculosis 70 0.221
26
ATH003 Atherosclerosis 63 0.221
27
HYP266 Hypoxia 55 0.203
28
c HPT003 Hepatitis a 55 0.198
29
P HRT032 Heart Disease 64 0.197
30
c ACT210 Acute Respiratory Distress Syndrome 55 0.193
31
ISC004 Ischemia 56 0.189
32
c SYS001 Systemic Lupus Erythematosus 87 0.189
33
P RSP003 Respiratory Failure 68 0.186
34
P LPS004 Lupus Erythematosus 63 0.185
35
CHL071 Child Syndrome 58 0.182
36
SRF006 Surfactant Dysfunction 32 0.181
37
KDS001 Kid Syndrome 53 0.181
38
P ADL010 Adult Respiratory Distress Syndrome 60 0.180
39
P PLM036 Pulmonary Fibrosis 69 0.179
40
INT066 Interstitial Lung Disease 60 0.178
41
P KDN018 Kidney Disease 64 0.177
42
RSP006 Respiratory System Disease 61 0.176
43
ALR002 Al-Raqad Syndrome 36 0.170
44
MCN007 Meconium Aspiration Syndrome 52 0.168
45
P PLM006 Pulmonary Alveolar Proteinosis 46 0.162
46
ADL002 Adult Syndrome 53 0.162
47
ADN018 Adenoma 59 0.156
48
BLD054 Blood Protein Disease 38 0.155
49
PCK002 Pick Disease 66 0.153
50
RSP019 Respiratory Distress Syndrome in Premature Infants 43 0.151
51
NWB001 Newborn Respiratory Distress Syndrome 47 0.149
52
P PSR002 Psoriasis 63 0.148
53
DRM006 Dermatitis 58 0.147
54
DMN002 Dementia 62 0.145
55
P MNN013 Meningitis 66 0.145
56
RSP007 Respiratory Distress Syndrome, Infant 26 0.143
57
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 57 0.143
58
BRN056 Bronchopulmonary Dysplasia 56 0.142
59
P PRD008 Periodontitis 46 0.140
60
CHR322 Choreoathetosis, Hypothyroidism, and Neonatal Respiratory Distress 43 0.139
61
CSY001 C Syndrome 49 0.138
62
CLT003 Colitis 56 0.135
63
PLM001 Pulmonary Tuberculosis 69 0.135
64
c CNG401 Congenital Heart Disease 67 0.134
65
P TCL004 T-Cell Leukemia 44 0.134
66
c ADL080 Adult Acute Respiratory Distress Syndrome 21 0.131
67
P INF032 Infertility 61 0.131
68
VCC001 Vaccinia 46 0.129
69
ACQ007 Acquired Immunodeficiency Syndrome 60 0.126
70
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.123
71
c BLD124 Bleeding Disorder, Platelet-Type, 11 37 0.122
72
P LYM026 Lymphoblastic Leukemia 60 0.121
73
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 41 0.115
74
ULC004 Ulcerative Colitis 74 0.115
75
CHL123 Chlamydia 60 0.113
76
PLM033 Pulmonary Embolism 59 0.112
77
P HYP086 Hypothyroidism 63 0.110
78
MSL001 Measles 61 0.107
79
ACD009 Acid-Labile Subunit, Deficiency of 37 0.107
80
BRN071 Brain Injury 51 0.107
81
BRN002 Bronchiolitis 56 0.106
82
P PLM037 Pulmonary Hypertension 78 0.105
83
DWN001 Down Syndrome 65 0.104
84
PLC008 Placenta Disease 33 0.103
85
ALL026 Allergic Hypersensitivity Disease 53 0.102
86
C3D001 C3 Deficiency 50 0.102
87
c SRF005 Surfactant Metabolism Dysfunction, Pulmonary, 3 29 0.102
88
NNT004 Neonatal Respiratory Failure 38 0.102
89
c SVR001 Severe Acute Respiratory Syndrome 56 0.101
90
P RHN004 Rhinitis 59 0.101
91
P ATP001 Atopic Dermatitis 60 0.099
92
DPH001 Diphtheria 55 0.099
93
c INH020 Inherited Metabolic Disorder 49 0.098
94
NSD001 Nose Disease 51 0.098
95
P HYP265 Hypotonia 39 0.096
96
P LNG064 Lung Cancer Susceptibility 3 62 0.094
97
ACR041 Acromelic Frontonasal Dysostosis 45 0.093
98
BRT030 Birth Defects 44 0.093
99
SKN023 Skin Tag 48 0.093
100
HMT018 Hematopoietic Stem Cell Transplantation 39 0.092
101
P RTT002 Rett Syndrome 77 0.092
102
MLD001 Melioidosis 67 0.091
103
P CNG015 Congenital Diaphragmatic Hernia 58 0.091
104
PLM034 Pulmonary Emphysema 55 0.090
105
P SPS003 Spastic Diplegia 49 0.089
106
RTN018 Retinal Disease 55 0.088
107
SCK005 Sickle Cell Disease 51 0.088
108
CRV047 Cervical Cancer, Somatic 65 0.087
109
EYD002 Eye Disease 62 0.087
110
WLL006 Wells Syndrome 57 0.087
111
GDS001 Good Syndrome 46 0.086
112
ALL003 Allergic Rhinitis 67 0.085
113
STM006 Stomach Disease 48 0.085
114
P SHR029 Short Syndrome 60 0.085
115
OTT002 Otitis Media 66 0.084
116
CRN246 Cranioosteoarthropathy 32 0.084
117
P SNS014 Sinusitis 66 0.084
118
ATP002 Atopy 62 0.084
119
P HYP071 Hypersensitivity Reaction Type Ii Disease 46 0.084
120
P TBR001 Tuberous Sclerosis 68 0.084
121
SKN016 Skin Disease 69 0.083
122
VND001 Vein Disease 51 0.083
123
LPD004 Lipoid Nephrosis 49 0.083
124
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 30 0.083
125
LSH001 Leishmaniasis 63 0.083
126
P NRV006 Nervous System Cancer 62 0.082
127
ADJ001 Adjustment Disorder 38 0.082
128
VGN023 Vaginitis 41 0.081
129
P ALX003 Alexander Disease 64 0.081
130
P ASP006 Aspergillosis 61 0.081
131
CHR005 Chorioamnionitis 47 0.080
132
P ESN007 Eosinophilia 61 0.080
133
P HMN010 Hemangioma 62 0.079
134
P RNL017 Renal Oncocytoma 48 0.078
135
c THR092 Thrombophilia Due to Thrombin Defect 56 0.078
136
PLM010 Pulmonary Edema 56 0.077
137
BRN038 Bronchial Disease 54 0.077
138
ATN011 Autoinflammation with Infantile Enterocolitis 36 0.077
139
TRC026 Tracheal Disease 33 0.075
140
P HRM001 Hermansky-Pudlak Syndrome 56 0.075
141
P UVT001 Uveitis 60 0.075
142
CYT008 Cytomegalovirus Infection 51 0.075
143
CHR177 Chromophobe Renal Cell Carcinoma 43 0.075
144
TXC005 Toxic Shock Syndrome 61 0.075
145
BRN024 Bronchitis 67 0.074
146
SLC006 Silicosis 53 0.073
147
CNT047 Contact Dermatitis 62 0.073
148
c ADL017 Adult T-Cell Leukemia 59 0.073
149
c AST037 Asthma 1 35 0.073
150
PRN029 Parainfluenza Virus Type 3 34 0.073
151
GLB003 Globe Disease 34 0.072
152
P DRM010 Dermatomyositis 59 0.071
153
P CRN178 Coronary Heart Disease 6 22 0.071
154
WST001 West Syndrome 61 0.070
155
SML020 Small Patella Syndrome 36 0.070
156
ALL006 Allergic Asthma 59 0.070
157
PLM012 Pulmonary Sarcoidosis 54 0.070
158
DRG003 Drug Dependence 53 0.070
159
ETH011 Ethylmalonic Encephalopathy 57 0.069
160
HDC001 Headache 52 0.069
161
BNF002 Bone Fracture 46 0.068
162
BRN022 Bronchiectasis 55 0.068
163
P TRN020 Turner Syndrome 64 0.068
164
c CRN214 Coronary Heart Disease 5 22 0.067
165
P PLY041 Polymyositis 49 0.067
166
PRP019 Peripheral Nervous System Disease 52 0.067
167
c TRC078 Trichohepatoenteric Syndrome 2 30 0.067
168
ATN005 Autonomic Dysfunction 44 0.064
169
PLM129 Pulmonary Disease, Chronic Obstructive 61 0.064
170
BRN012 Bronchiolitis Obliterans 58 0.064
171
P DRV001 Dravet Syndrome 66 0.063
172
NSY001 N Syndrome 42 0.063
173
c AST039 Asthma 2 28 0.063
174
CRB085 Cerebral Hemorrhage 40 0.063
175
LRY017 Laryngeal Disease 33 0.062
176
P ESN008 Eosinophilic Pneumonia 47 0.062
177
c VRL005 Viral Pneumonia 44 0.062
178
UPP004 Upper Respiratory Tract Disease 48 0.061
179
PRT056 Protein R Deficiency 12 0.060
180
STF001 Stiff-Person Syndrome 54 0.060
181
c LRG001 Large Cell Carcinoma 49 0.060
182
CRY005 Cryptococcosis 50 0.060
183
STC004 Stachybotrys Chartarum 38 0.060
184
PTN001 Patent Foramen Ovale 55 0.060
185
CCN007 Cocoon Syndrome 32 0.059
186
c CNG006 Congenital Hypothyroidism 59 0.058
187
P DGR001 Digeorge Syndrome 52 0.057
188
ANG049 Angioedema Induced by Ace Inhibitors 35 0.057
189
CRB037 Cerebral Palsy 54 0.057
190
EXT034 Extrinsic Allergic Alveolitis 58 0.057
191
MYC073 Mycobacterium Tuberculosis, Susceptibility to Mycobacterium Tuberculosis, Protection Against, Included 36 0.056
192
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 60 0.056
193
P LYM007 Lymphangioleiomyomatosis 65 0.056
194
SKN027 Skin Conditions 44 0.056
195
RBR001 Roberts Syndrome 61 0.054
196
TTR001 Tetralogy of Fallot 69 0.054
197
ALL010 Allergic Contact Dermatitis 58 0.054
198
MSS002 Mass Syndrome 49 0.053
199
c CRN173 Coronary Heart Disease 8 19 0.053
200
PLM122 Pulmonary Hypertension, Familial Primary, 1, with or Without Hht 45 0.053
201
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 42 0.053
202
MVD001 Moved to 60 0.052
203
P ART084 Arteriovenous Fistula 40 0.052
204
ATN002 Autonomic Nervous System Disease 46 0.051
205
P HMP006 Hemiplegic Migraine 45 0.051
206
PRD011 Proud Syndrome 42 0.051
207
c FML001 Familial Atrial Fibrillation 59 0.050
208
NRF007 Neurofibroma 53 0.050
209
HMP005 Hemiplegia 52 0.049
210
c MLG077 Malignant Peripheral Nerve Sheath Tumor 56 0.049
211
BCK006 Back Pain 40 0.049
212
OCY001 Oocyte Maturation Defect 31 0.049
213
WLL001 Williams-Beuren Syndrome 61 0.048
214
c INV001 Invasive Aspergillosis 44 0.047
215
SLD003 Sialadenitis 45 0.047
216
GNT003 Genital Herpes 55 0.046
217
ACT017 Acute Chest Syndrome 50 0.046
218
FRM003 Farmer's Lung 47 0.046
219
P VNT002 Ventricular Septal Defect 59 0.045
220
P VLC001 Velocardiofacial Syndrome 64 0.044
221
CLD014 Cole Disease 38 0.044
222
VNT001 Ventilation Pneumonitis 35 0.044
223
P SML002 Small Cell Sarcoma 39 0.044
224
PLM134 Pulmonary Fibrosis, Idiopathic 61 0.043
225
c CHR096 Chronic Pulmonary Heart Disease 40 0.043
226
ASP003 Aseptic Meningitis 51 0.043
227
LNS003 Lens Disease 37 0.042
228
DCB001 Decubitus Ulcer 44 0.042
229
HPT009 Hepatopulmonary Syndrome 48 0.041
230
P EPS003 Episodic Ataxia 58 0.041
231
PLM017 Pulmonary Alveolar Microlithiasis 46 0.041
232
P IGN003 Iga Nephropathy 1 31 0.041
233
P SYS005 Systemic Scleroderma 60 0.041
234
BRN118 Brain Small Vessel Disease with or Without Ocular Anomalies 42 0.040
235
FCT008 Factitious Disorder 42 0.038
236
c PLM128 Pulmonary Hypertension, Primary, 2 36 0.038
237
P PNM006 Pneumoconiosis 51 0.038
238
BLL003 Bell's Palsy 47 0.036
239
P ICH001 Ichthyosis Vulgaris 44 0.036
240
HRT012 Heart Valve Disease 39 0.035
241
P TMT001 Timothy Syndrome 58 0.035
242
LPD027 Lip Disease 35 0.035
243
c PLM127 Pulmonary Hypertension, Primary, 3 31 0.033