Search results for "hypoalphalipoproteinemias"

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

41 hits were found for 'hypoalphalipoproteinemias'

# Family MCID Name MIFTS Score
1
HYP121 Hypoalphalipoproteinemia 60 8.835
2
TNG002 Tangier Disease 63 5.395
3
APL025 Apolipoprotein a-I Deficiency 41 3.777
4
P HYP117 Hypertriglyceridemia 65 0.173
5
P CRN211 Coronary Artery Disease 74 0.142
6
ART111 Artery Disease 61 0.142
7
FSH001 Fish-Eye Disease 44 0.142
8
P HPT021 Hepatitis 77 0.123
9
P HRT032 Heart Disease 68 0.123
10
EYD002 Eye Disease 65 0.123
11
ATH003 Atherosclerosis 65 0.123
12
P OBS005 Obesity 91 0.100
13
P AMY004 Amyloidosis 68 0.100
14
NRM003 Norum Disease 54 0.100
15
P HYP090 Hyperalphalipoproteinemia 52 0.100
16
HYP037 Hyperhomocysteinemia 50 0.100
17
HYP081 Hypolipoproteinemia 46 0.100
18
END072 Endotheliitis 45 0.100
19
HPT025 Hepatic Lipase Deficiency 44 0.100
20
CRZ001 Crouzon Syndrome 70 0.071
21
AND015 Androgen Insensitivity 63 0.071
22
P AXN010 Axenfeld-Rieger Syndrome, Type 3 56 0.071
23
ALS001 Alstrom Syndrome 50 0.071
24
c LPD037 Lipodystrophy, Familial Partial, 2 47 0.071
25
HYP286 Hyperchylomicronemia, Late-Onset 44 0.071
26
c NMN016 Niemann-Pick Disease, Type B 40 0.071
27
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 38 0.071
28
ALN001 Aland Island Eye Disease 37 0.071
29
HPT074 Hepatic Adenoma, Somatic 36 0.071
30
c SRC023 Sarcoidosis 2 35 0.071
31
c JVN024 Juvenile Hereditary Hemochromatosis 35 0.071
32
AMS002 Amish Infantile Epilepsy Syndrome 35 0.071
33
c LPD021 Lipodystrophy, Familial Partial, Type 3 31 0.071
34
ALR002 Al-Raqad Syndrome 27 0.071
35
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 26 0.071
36
P LKN019 Leukoencephalopathy, Diffuse Hereditary, with Spheroids 26 0.071
37
LGP003 Logopenic Progressive Aphasia 23 0.071
38
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 22 0.071
39
ADL087 Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia 21 0.071
40
AND005 Androgen Insensitivity Syndrome, Mild 21 0.071
41
MRB006 Morbid Obesity and Spermatogenic Failure 17 0.071