Search results for abca3

168 hits were found for abca3

# Family MCID Name MIFTS Score
1
c SRF005 Surfactant Metabolism Dysfunction, Pulmonary, 3 35 75.525
2
LNG099 Lung Disease 62 30.137
3
INT066 Interstitial Lung Disease 60 26.957
4
P RSP003 Respiratory Failure 74 23.675
5
PLM134 Pulmonary Fibrosis, Idiopathic 76 23.606
6
c PRM166 Primary Interstitial Lung Disease Specific to Childhood Due to Pulmonary Surfactant Protein Anomalies 8 21.039
7
P PLM037 Pulmonary Hypertension 72 18.481
8
P PLM036 Pulmonary Fibrosis 66 18.185
9
P ADL010 Adult Respiratory Distress Syndrome 71 15.582
10
NWB001 Newborn Respiratory Distress Syndrome 56 14.822
11
SRF006 Surfactant Dysfunction 33 14.515
12
NNT004 Neonatal Respiratory Failure 36 14.205
13
c PLM164 Pulmonary Hypertension, Primary, 1 76 12.749
14
RSP007 Respiratory Distress Syndrome, Infant 40 12.387
15
ACT029 Acute Interstitial Pneumonia 59 11.703
16
RSP019 Respiratory Distress Syndrome in Premature Infants 52 11.122
17
P ICH004 Ichthyosis 56 10.837
18
P PSD087 Pseudoxanthoma Elasticum 67 10.679
19
CTR014 Cataract Microcornea Syndrome 35 8.856
20
DFF002 Diffuse Pulmonary Fibrosis 27 8.717
21
P SRF004 Surfactant Metabolism Dysfunction, Pulmonary, 1 43 8.275
22
PLM022 Pulmonary Valve Insufficiency 45 8.275
23
c ATS013 Autosomal Recessive Congenital Ichthyosis 66 7.849
24
c ICH069 Ichthyosis, Congenital, Autosomal Recessive 4b 52 7.663
25
MCN007 Meconium Aspiration Syndrome 53 7.663
26
INT304 Interstitial Pneumonitis, Desquamative, Familial 42 7.419
27
PLM013 Pulmonary Immaturity 31 7.419
28
LYS003 Lysinuric Protein Intolerance 57 6.832
29
P INT354 Interstitial Lung Disease Specific to Childhood 8 6.832
30
c OST127 Osteogenesis Imperfecta, Type X 38 6.832
31
P PLM085 Pulmonary Hemosiderosis 44 6.832
32
PLM017 Pulmonary Alveolar Microlithiasis 47 6.832
33
ISC020 Ischiocoxopodopatellar Syndrome with or Without Pulmonary Arterial Hypertension 51 6.832
34
CNG184 Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects 56 6.832
35
LPD001 Lipid Pneumonia 29 6.832
36
INT011 Interstitial Emphysema 33 6.832
37
HYP081 Hypolipoproteinemia 49 6.832
38
NNS002 Nonspecific Interstitial Pneumonia 42 6.832
39
CHR058 Chronic Congestive Splenomegaly 26 6.832
40
VNT001 Ventilation Pneumonitis 23 6.832
41
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 4.844
42
P LKM062 Leukemia, Acute Lymphoblastic 69 4.766
43
P MYL006 Myeloid Leukemia 61 4.111
44
c LKM061 Leukemia, Acute Myeloid 83 3.790
45
P LKM002 Leukemia 67 3.695
46
P LNG032 Lung Cancer 98 3.399
47
P BRS047 Breast Cancer 98 2.966
48
c SML038 Small Cell Cancer of the Lung 69 2.907
49
GNT107 Genetic Interstitial Lung Disease 8 2.907
50
P PLM006 Pulmonary Alveolar Proteinosis 53 2.907
51
P PNM007 Pneumonia 67 2.665
52
P LNG064 Lung Cancer Susceptibility 3 70 2.658
54
P KLZ004 Kala-Azar 1 41 2.567
55
LSH001 Leishmaniasis 64 2.567
56
CHL079 Children's Interstitial Lung Disease 26 2.567
57
CHL149 Childhood Acute Myeloid Leukemia 43 2.472
58
c LKM063 Leukemia, Chronic Myeloid 71 2.371
59
CYN002 Cyanosis, Transient Neonatal 43 2.371
60
CTN007 Cutaneous Leishmaniasis 62 2.371
61
BRN056 Bronchopulmonary Dysplasia 56 2.371
62
47X002 47,xyy 48 2.264
63
PCT003 Pectus Excavatum 46 2.149
64
SCN068 Secondary Interstitial Lung Disease in Childhood and Adulthood Associated with a Connective Tissue Disease 19 2.023
65
CNN005 Connective Tissue Disease 67 2.023
66
P CTR002 Cataract 60 2.023
67
CYS001 Cystic Fibrosis 78 1.947
68
P PRS040 Prostate Cancer 95 1.935
69
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 49 1.922
70
DFF005 Diffuse Large B-Cell Lymphoma 54 1.805
71
P BCL017 B-Cell Lymphoma 59 1.761
72
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 1.661
73
CHL152 Childhood Acute Lymphocytic Leukemia 50 1.661
74
P CHL156 Childhood T-Cell Acute Lymphoblastic Leukemia 38 1.661
75
PLM108 Pulmonary Interstitial Glycogenosis 17 1.661
76
P GLY013 Glycogen Storage Disease 60 1.661
77
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 1.661
78
TNG002 Tangier Disease 64 1.438
79
c PLM044 Pulmonary Fibrosis, Familial 18 1.438
81
P LYM118 Lymphoma 67 1.313
82
NRN023 Neuroendocrine Cell Hyperplasia of Infancy 15 1.313
83
ACS001 Acoustic Neuroma 56 1.174
84
P HYP083 Hypopituitarism 52 1.174
85
P HYP086 Hypothyroidism 69 1.174
86
IDP011 Idiopathic Interstitial Pneumonia 59 1.174
87
NRL005 Neurilemmoma 60 1.174
88
P OVR042 Ovarian Cancer 88 1.079
89
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.017
91
RTN020 Retinal Vascular Disease 46 1.017
93
BRS099 Breast Ductal Carcinoma 61 0.978
94
c CNG121 Congenital Pulmonary Alveolar Proteinosis 16 0.940
95
c HRD171 Hereditary Pulmonary Alveolar Proteinosis 38 0.830
96
P LYM033 Lymphoproliferative Syndrome 59 0.830
97
KWS002 Kawasaki Disease 65 0.830
98
ALV007 Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins 48 0.830
99
CHL065 Cholangiocarcinoma 58 0.830
100
P NRB001 Neuroblastoma 66 0.830
101
P MSC005 Muscular Dystrophy 67 0.830
102
SVR001 Severe Acute Respiratory Syndrome 67 0.830
103
PNM008 Pneumothorax 54 0.830
104
ADN018 Adenoma 59 0.830
105
P GLL022 Guillain-Barre Syndrome 60 0.830
106
BRN012 Bronchiolitis Obliterans 56 0.830
107
INT079 Intrahepatic Cholangiocarcinoma 51 0.830
108
BRN002 Bronchiolitis 57 0.830
109
ADL002 Adult Syndrome 70 0.747
110
ANT039 Antisynthetase Syndrome 55 0.747
111
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.747
112
P EPL140 Epilepsy, Idiopathic Generalized 62 0.712
113
END057 Endometrial Cancer 72 0.712
114
c HYP708 Hyperaldosteronism, Familial, Type Iv 30 0.712
115
P PNC035 Pancreatic Cancer 86 0.696
116
LMN016 Luminal Breast Carcinoma B 28 0.691
117
P LMN015 Luminal Breast Carcinoma a 35 0.691
118
ESP021 Esophageal Cancer 83 0.691
119
ESP027 Esophagus Squamous Cell Carcinoma 45 0.691
120
INT351 Interstitial Lung Disease Specific to Infancy 6 0.587
121
ADR022 Adrenomyeloneuropathy 39 0.587
122
ADR007 Adrenoleukodystrophy 73 0.587
123
c THY107 Thymoma, Familial 42 0.587
124
c HRM005 Hermansky-Pudlak Syndrome 1 55 0.587
125
c ICH040 Ichthyosis, Congenital, Autosomal Recessive 4a 41 0.587
126
CRV035 Cervical Cancer 73 0.587
127
CHR630 Chorea, Benign Hereditary 41 0.587
128
P CLR023 Colorectal Cancer 100 0.587
129
CHR005 Chorioamnionitis 50 0.587
130
HYP458 Hyper Ige Syndrome 60 0.587
131
CLT003 Colitis 63 0.587
132
c CNG006 Congenital Hypothyroidism 63 0.587
133
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 0.587
134
P STN012 Sting-Associated Vasculopathy, Infantile-Onset 42 0.587
135
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 0.587
136
ALP103 Alpha-1-Antitrypsin Deficiency 68 0.587
137
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.587
138
P HPT023 Hepatocellular Carcinoma 96 0.587
139
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.587
140
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.587
141
P PTN014 Patent Ductus Arteriosus 1 59 0.587
142
STN011 Sting-Associated Vasculopathy with Onset in Infancy 45 0.587
143
ULC004 Ulcerative Colitis 74 0.587
144
c BCT013 Bacterial Pneumonia 48 0.587
145
c PRM316 Primary Congenital Hypothyroidism 32 0.587
146
SKN016 Skin Disease 63 0.587
147
PNC129 Pancreatic Adenocarcinoma 65 0.587
148
HST010 Histiocytosis 49 0.587
149
P HRM001 Hermansky-Pudlak Syndrome 65 0.587
150
PRT011 Protein C Deficiency 47 0.587
151
P INF038 Influenza 68 0.587
152
EXT034 Extrinsic Allergic Alveolitis 57 0.587
153
P PLM179 Pulmonary Alveolar Proteinosis with Hypogammaglobulinemia 16 0.587
154
CHG001 Chagas Disease 66 0.587
155
SYN005 Synostosis 43 0.587
156
P ADN016 Adenocarcinoma 63 0.587
157
P AGM001 Agammaglobulinemia 68 0.587
158
P KDN017 Kidney Cancer 61 0.587
159
P THY023 Thymoma 64 0.587
160
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.587
161
INT046 Intestinal Tuberculosis 39 0.587
162
CHR073 Choreatic Disease 54 0.587
163
P BRN022 Bronchiectasis 60 0.587
164
STT071 Stat3 Hyper Ige Syndrome 19 0.587
165
HRT015 Heritable Pulmonary Arterial Hypertension 46 0.587
166
STR046 Stargardt Macular Degeneration 27 0.587
167
HYP266 Hypoxia 57 0.587
168
P GLM040 Glioma Susceptibility 1 71 0.492
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