Search results for "hypoalphalipoproteinemias"

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

50 hits were found for 'hypoalphalipoproteinemias'

# Family MCID Name MIFTS Score
1
HYP121 Hypoalphalipoproteinemia 61 10.380
2
TNG002 Tangier Disease 62 5.618
3
P HYP117 Hypertriglyceridemia 61 0.162
4
FSH001 Fish-Eye Disease 43 0.162
5
P CRN211 Coronary Artery Disease 74 0.132
6
ART111 Artery Disease 55 0.132
7
P HRT032 Heart Disease 75 0.115
8
P HPT021 Hepatitis 69 0.115
9
ATH003 Atherosclerosis 65 0.115
10
EYD002 Eye Disease 61 0.115
11
c HYP163 Hyperlipidemia Type 3 36 0.115
12
P OBS005 Obesity 92 0.094
13
P AMY004 Amyloidosis 65 0.094
14
HYP037 Hyperhomocysteinemia 50 0.094
15
P HYP090 Hyperalphalipoproteinemia 48 0.094
16
HPT025 Hepatic Lipase Deficiency 48 0.094
17
HYP081 Hypolipoproteinemia 42 0.094
18
END072 Endotheliitis 42 0.094
19
CRZ001 Crouzon Syndrome 70 0.066
20
AND015 Androgen Insensitivity 64 0.066
21
LPD008 Lipid Metabolism Disorder 58 0.066
22
ETH011 Ethylmalonic Encephalopathy 56 0.066
23
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.066
24
ALS001 Alstrom Syndrome 53 0.066
25
c LPD037 Lipodystrophy, Familial Partial, 2 52 0.066
26
NRM003 Norum Disease 51 0.066
27
HPT074 Hepatic Adenoma, Somatic 50 0.066
28
CSY001 C Syndrome 50 0.066
29
c EHL032 Ehlers-Danlos Syndrome, Type Viib 49 0.066
30
P LKN019 Leukoencephalopathy, Diffuse Hereditary, with Spheroids 49 0.066
31
HYP286 Hyperchylomicronemia, Late-Onset 45 0.066
32
ALN001 Aland Island Eye Disease 45 0.066
33
c NMN016 Niemann-Pick Disease, Type B 43 0.066
34
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 39 0.066
35
ALR002 Al-Raqad Syndrome 36 0.066
36
AMS002 Amish Infantile Epilepsy Syndrome 35 0.066
37
ADP007 Adie Pupil 34 0.066
38
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 33 0.066
39
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 33 0.066
40
c SRC023 Sarcoidosis 2 33 0.066
41
c HYP272 Hypercholesterolemia, Familial, 3 32 0.066
42
c LPD021 Lipodystrophy, Familial Partial, Type 3 32 0.066
43
P ATX010 Ataxia Neuropathy Spectrum 30 0.066
44
c HYP555 Hypertriglyceridemia, Transient Infantile 29 0.066
45
NMN003 Niemann–pick Disease 26 0.066
46
HNM002 Hinman Syndrome 25 0.066
47
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 25 0.066
48
LGP003 Logopenic Progressive Aphasia 22 0.066
49
MRB006 Morbid Obesity and Spermatogenic Failure 16 0.066
50
AND005 Androgen Insensitivity Syndrome, Mild 16 0.066