Search results for "hypoalphalipoproteinemias"

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

49 hits were found for 'hypoalphalipoproteinemias'

# Family MCID Name MIFTS Score
1
HYP121 Hypoalphalipoproteinemia 61 10.361
2
TNG002 Tangier Disease 61 5.610
3
P HYP117 Hypertriglyceridemia 65 0.162
4
FSH001 Fish-Eye Disease 43 0.148
5
P CRN211 Coronary Artery Disease 75 0.133
6
ART111 Artery Disease 57 0.133
7
P HRT032 Heart Disease 76 0.115
8
P HPT021 Hepatitis 70 0.115
9
EYD002 Eye Disease 63 0.115
10
ATH003 Atherosclerosis 62 0.115
11
P OBS005 Obesity 93 0.094
12
P AMY004 Amyloidosis 64 0.094
13
HYP037 Hyperhomocysteinemia 50 0.094
14
HPT025 Hepatic Lipase Deficiency 48 0.094
15
P HYP090 Hyperalphalipoproteinemia 46 0.094
16
END072 Endotheliitis 42 0.094
17
HYP081 Hypolipoproteinemia 41 0.094
18
CRZ001 Crouzon Syndrome 70 0.066
19
P CWD006 Cowden Syndrome 1 68 0.066
20
AND015 Androgen Insensitivity 63 0.066
21
ETH011 Ethylmalonic Encephalopathy 59 0.066
22
LPD008 Lipid Metabolism Disorder 58 0.066
23
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.066
24
ALS001 Alstrom Syndrome 52 0.066
25
NRM003 Norum Disease 52 0.066
26
c LPD037 Lipodystrophy, Familial Partial, 2 51 0.066
27
HPT074 Hepatic Adenoma, Somatic 51 0.066
28
CSY001 C Syndrome 49 0.066
29
P LKN019 Leukoencephalopathy, Diffuse Hereditary, with Spheroids 48 0.066
30
HYP286 Hyperchylomicronemia, Late-Onset 46 0.066
31
ALN001 Aland Island Eye Disease 45 0.066
32
c NMN016 Niemann-Pick Disease, Type B 45 0.066
33
ALR002 Al-Raqad Syndrome 36 0.066
34
c HYP272 Hypercholesterolemia, Familial, 3 35 0.066
35
AMS002 Amish Infantile Epilepsy Syndrome 35 0.066
36
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 34 0.066
37
ADP007 Adie Pupil 34 0.066
38
c HYP163 Hyperlipidemia Type 3 34 0.066
39
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 34 0.066
40
c SRC023 Sarcoidosis 2 33 0.066
41
c LPD021 Lipodystrophy, Familial Partial, Type 3 30 0.066
42
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 30 0.066
43
c HYP555 Hypertriglyceridemia, Transient Infantile 29 0.066
44
P ATX010 Ataxia Neuropathy Spectrum 28 0.066
45
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 25 0.066
46
HNM002 Hinman Syndrome 25 0.066
47
LGP003 Logopenic Progressive Aphasia 22 0.066
48
MRB006 Morbid Obesity and Spermatogenic Failure 16 0.066
49
AND005 Androgen Insensitivity Syndrome, Mild 16 0.066