Search results for "hypoalphalipoproteinemias"

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

145 hits were found for 'hypoalphalipoproteinemias'

# Family MCID Name MIFTS Score
1
HYP121 Hypoalphalipoproteinemia 55 7.856
2
TNG002 Tangier Disease 59 5.252
3
APL025 Apolipoprotein a-I Deficiency 34 3.700
4
P MYC007 Myocardial Infarction 77 0.084
5
P HPT021 Hepatitis 63 0.084
6
HPT023 Hepatocellular Carcinoma 87 0.068
7
P ART022 Arthritis 63 0.068
8
P HRT032 Heart Disease 58 0.068
9
P HYP117 Hypertriglyceridemia 58 0.068
10
ADN018 Adenoma 53 0.068
11
P PNC044 Pancreatitis 53 0.068
12
c ACT075 Acute Myocardial Infarction 51 0.068
13
P ATX004 Ataxia 43 0.068
14
END072 Endotheliitis 41 0.068
15
HYP081 Hypolipoproteinemia 37 0.068
16
NRN002 Neuronitis 36 0.068
17
P LNG032 Lung Cancer 91 0.048
18
P OBS005 Obesity 87 0.048
19
P RHM011 Rheumatoid Arthritis 87 0.048
20
c SYS001 Systemic Lupus Erythematosus 84 0.048
21
CYS001 Cystic Fibrosis 84 0.048
22
P PNC035 Pancreatic Cancer 82 0.048
23
P PLM037 Pulmonary Hypertension 78 0.048
24
P AST005 Asthma 77 0.048
25
P CRN211 Coronary Artery Disease 69 0.048
26
P MDL005 Medulloblastoma 68 0.048
27
FBR012 Fabry Disease 67 0.048
28
P INF038 Influenza 67 0.048
29
P KRT004 Keratitis 66 0.048
30
P CLC005 Celiac Disease 63 0.048
31
P LKM002 Leukemia 63 0.048
32
LNG024 Langerhans-Cell Histiocytosis 61 0.048
33
P LVR013 Liver Disease 60 0.048
34
P ATR011 Atrial Fibrillation 59 0.048
35
PRP027 Peripheral Vascular Disease 59 0.048
36
P AMY004 Amyloidosis 59 0.048
37
P CRD011 Cardiomyopathy 59 0.048
38
P LPS004 Lupus Erythematosus 59 0.048
39
PRT037 Pertussis 59 0.048
40
P ADN016 Adenocarcinoma 59 0.048
41
P PLY011 Polycystic Ovary Syndrome 58 0.048
42
ISC006 Ischemic Heart Disease 58 0.048
43
P PSR002 Psoriasis 58 0.048
44
c HPT016 Hepatitis B 57 0.048
45
P PRD008 Periodontitis 57 0.048
46
QFV001 Q Fever 56 0.048
47
ACN011 Acne 55 0.048
48
VSC007 Vascular Disease 55 0.048
49
P GST044 Gastritis 55 0.048
50
MLN008 Melanoma 55 0.048
51
P THR015 Thrombophilia 54 0.048
52
CHL014 Cholera 54 0.048
53
WLL001 Williams-Beuren Syndrome 54 0.048
54
HST011 Histoplasmosis 54 0.048
55
P MSC005 Muscular Dystrophy 54 0.048
56
DNY001 Denys-Drash Syndrome 54 0.048
57
P ESP024 Esophagitis 54 0.048
58
CCC001 Coccidioidomycosis 53 0.048
59
P HST010 Histiocytosis 53 0.048
60
c ACT027 Acute Pancreatitis 53 0.048
61
P CRB042 Cerebellar Ataxia 52 0.048
62
PRD007 Periodontal Disease 52 0.048
63
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.048
64
HPT022 Hepatoblastoma 52 0.048
65
ALS001 Alstrom Syndrome 51 0.048
66
c THR092 Thrombophilia Due to Thrombin Defect 51 0.048
67
P DYS154 Dystonia 51 0.048
68
P LMB006 Limb-Girdle Muscular Dystrophy 51 0.048
69
P MMP001 Mumps 50 0.048
70
NRM003 Norum Disease 50 0.048
71
P PRM006 Primary Biliary Cirrhosis 50 0.048
72
P MYL007 Myeloma 50 0.048
73
P HYP040 Hypospadias 49 0.048
74
c ACT073 Acute Leukemia 49 0.048
75
ART111 Artery Disease 49 0.048
76
P PRS038 Personality Disorder 49 0.048
77
VTR013 Vitreoretinopathy, Neovascular Inflammatory 48 0.048
78
c LPD037 Lipodystrophy, Familial Partial, 2 48 0.048
79
BLM002 Bulimia Nervosa 48 0.048
80
P CTR002 Cataract 47 0.048
81
ING001 Inguinal Hernia 47 0.048
82
AVN001 Avian Influenza 46 0.048
83
ANR040 Aneurysm 46 0.048
84
P GLM045 Glioma 46 0.048
85
FSH001 Fish-Eye Disease 45 0.048
86
c MLG068 Malignant Glioma 44 0.048
87
SNS001 Sensorineural Hearing Loss 44 0.048
88
KDS001 Kid Syndrome 44 0.048
89
GST053 Gastric Cancer 44 0.048
90
LYM027 Lymphopenia 44 0.048
91
P LPD010 Lipodystrophy 43 0.048
92
RST001 Restless Legs Syndrome 42 0.048
93
BLS002 Blastomycosis 42 0.048
94
PRT082 Preterm Premature Rupture of the Membranes 42 0.048
95
P STR020 Strabismus 42 0.048
96
FBR032 Fibromuscular Dysplasia 42 0.048
97
TRC008 Trachoma 41 0.048
98
SLL001 Sialolithiasis 41 0.048
99
THR013 Thoracic Outlet Syndrome 41 0.048
100
CRT013 Carotid Stenosis 41 0.048
101
c NMN016 Niemann-Pick Disease, Type B 40 0.048
102
TRN007 Transsexualism 38 0.048
103
TRN012 Transient Global Amnesia 38 0.048
104
SYN036 Syncope 38 0.048
105
URT001 Urethritis 37 0.048
106
PRT026 Parotitis 37 0.048
107
HYP286 Hyperchylomicronemia, Late-Onset 36 0.048
108
GLM011 Glomerulosclerosis 36 0.048
109
AMB002 Amblyopia 36 0.048
110
DYS015 Dysentery 36 0.048
111
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 36 0.048
112
SNL007 Senile Cataract 35 0.048
113
TBR009 Tuberculous Empyema 35 0.048
114
P CHN006 Chondromalacia Patellae 35 0.048
115
BLR015 Blue Rubber Bleb Nevus Syndrome 34 0.048
116
ACR005 Acrodermatitis 33 0.048
117
URT016 Urethral Diverticulum 32 0.048
118
OLG001 Oligospermia 32 0.048
119
NPH001 Nephrogenic Adenoma 32 0.048
120
c LPD021 Lipodystrophy, Familial Partial, Type 3 32 0.048
121
HPT074 Hepatic Adenoma, Somatic 31 0.048
122
SPS057 Spasticity 31 0.048
123
P INT063 Intellectual Disability 31 0.048
124
AMY002 Amyloid Tumor 31 0.048
125
CHN011 Chondromalacia 30 0.048
126
P LKN019 Leukoencephalopathy, Diffuse Hereditary, with Spheroids 30 0.048
127
AYM001 Ayme-Gripp Syndrome 29 0.048
128
VNF001 Vein of Galen Aneurysm 27 0.048
129
ANS004 Anisometropia 26 0.048
130
BRN055 Bronchogenic Cyst 26 0.048
131
P SPS008 Spastic Ataxia 24 0.048
132
ALR002 Al-Raqad Syndrome 24 0.048
133
TNB001 Tinea Barbae 23 0.048
134
NRS005 Neurosarcoidosis 23 0.048
135
MYX011 Myxozoa 23 0.048
136
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 23 0.048
137
PRF003 Piriformis Syndrome 22 0.048
138
LGP003 Logopenic Progressive Aphasia 21 0.048
139
SCR025 Scarf Syndrome 20 0.048
140
c BNG076 Benign Exophthalmos Syndrome 17 0.048
141
SPT015 Septate Vagina 17 0.048
142
AND005 Androgen Insensitivity Syndrome, Mild 17 0.048
143
MRB006 Morbid Obesity and Spermatogenic Failure 16 0.048
144
ADL087 Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia 15 0.048
145
c SLC030 Slc6a4-Related Altered Drug Metabolism 14 0.048