Search results for "hypoalphalipoproteinemias"

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

42 hits were found for 'hypoalphalipoproteinemias'

# Family MCID Name MIFTS Score
1
HYP121 Hypoalphalipoproteinemia 61 10.790
2
TNG002 Tangier Disease 61 5.652
3
P HYP117 Hypertriglyceridemia 65 0.183
4
FSH001 Fish-Eye Disease 44 0.170
5
P CRN211 Coronary Artery Disease 74 0.155
6
ART111 Artery Disease 56 0.155
7
P HPT021 Hepatitis 74 0.139
8
EYD002 Eye Disease 62 0.139
9
ATH003 Atherosclerosis 63 0.139
10
P HRT032 Heart Disease 64 0.139
11
P OBS005 Obesity 91 0.120
12
HPT025 Hepatic Lipase Deficiency 45 0.120
13
P HYP090 Hyperalphalipoproteinemia 45 0.120
14
P AMY004 Amyloidosis 63 0.120
15
HYP081 Hypolipoproteinemia 42 0.120
16
HYP037 Hyperhomocysteinemia 49 0.120
17
END072 Endotheliitis 41 0.120
18
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.098
19
ETH011 Ethylmalonic Encephalopathy 57 0.098
20
CRZ001 Crouzon Syndrome 70 0.098
21
AND015 Androgen Insensitivity 64 0.098
22
P LKN019 Leukoencephalopathy, Diffuse Hereditary, with Spheroids 38 0.098
23
AMS002 Amish Infantile Epilepsy Syndrome 34 0.098
24
CSY001 C Syndrome 49 0.098
25
c HYP555 Hypertriglyceridemia, Transient Infantile 26 0.098
26
HPT074 Hepatic Adenoma, Somatic 35 0.098
27
ALN001 Aland Island Eye Disease 45 0.098
28
HYP327 Hypertension, Early-Onset, Autosomal Dominant, with Exacerbation in Pregnancy 27 0.098
29
ALR002 Al-Raqad Syndrome 36 0.098
30
LGP003 Logopenic Progressive Aphasia 21 0.098
31
c JVN024 Juvenile Hereditary Hemochromatosis 30 0.098
32
OTP003 Oto-Palatal-Digital Syndrome 14 0.098
33
c LPD037 Lipodystrophy, Familial Partial, 2 52 0.069
34
ALS001 Alstrom Syndrome 52 0.069
35
HYP286 Hyperchylomicronemia, Late-Onset 45 0.069
36
c NMN016 Niemann-Pick Disease, Type B 43 0.069
37
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 26 0.069
38
NRM003 Norum Disease 53 0.069
39
c LPD021 Lipodystrophy, Familial Partial, Type 3 31 0.069
40
c HYP163 Hyperlipidemia Type 3 52 0.069
41
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 41 0.069
42
MRB006 Morbid Obesity and Spermatogenic Failure 17 0.069