Search results for "hypouricemia"

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

53 hits were found for 'hypouricemia'

# Family MCID Name MIFTS Score
1
P RNL042 Renal Hypouricemia 36 8.359
2
c RNL053 Renal Hypouricemia 2 12 5.253
3
c RNL052 Renal Hypouricemia 1 7 3.714
4
HYP017 Hypophosphatemia 49 0.132
5
P FNC004 Fanconi Syndrome 50 0.114
6
CHL065 Cholangiocarcinoma 69 0.093
7
c NPH012 Nephrotic Syndrome 67 0.093
8
P GT001 Gout 66 0.093
9
ISC004 Ischemia 63 0.093
10
c SVR001 Severe Acute Respiratory Syndrome 59 0.093
11
PRN001 Purine Nucleoside Phosphorylase Deficiency 59 0.093
12
P NPH009 Nephrolithiasis 58 0.093
13
P HYP014 Hyperuricemia 56 0.093
14
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 51 0.093
15
HYP005 Hypokalemia 50 0.093
16
IDP033 Idiopathic Edema 32 0.093
17
P ACT019 Acute Myeloid Leukemia 93 0.066
18
P LVR011 Liver Cancer 91 0.066
19
P ATX002 Ataxia Telangiectasia 87 0.066
20
AND002 Androgen Insensitivity Syndrome 80 0.066
21
P PNM007 Pneumonia 78 0.066
22
P LKM002 Leukemia 77 0.066
23
c MYL006 Myeloid Leukemia 75 0.066
24
c DBT009 Diabetes Mellitus 74 0.066
25
c PRM002 Primary Hyperoxaluria 74 0.066
26
P MTB001 Metabolic Syndrome X 70 0.066
27
c AXN002 Axenfeld-Rieger Syndrome 67 0.066
28
c AMY001 Amyotrophic Lateral Sclerosis 67 0.066
29
ACN002 Acanthosis Nigricans 63 0.066
30
c AMY077 Amyotrophic Lateral Sclerosis Type 18 60 0.066
31
MYC002 Mycobacterium Avium Complex Disease 59 0.066
32
BRN029 Brain Disease 58 0.066
33
P AMY074 Amyotrophic Lateral Sclerosis Type 14 56 0.066
34
ART001 Arterial Tortuosity Syndrome 55 0.066
35
c ACR001 Aicardi-Goutieres Syndrome 54 0.066
36
AND003 Andersen-Tawil Syndrome 54 0.066
37
THR013 Thoracic Outlet Syndrome 52 0.066
38
P PND001 Pain Disorder 52 0.066
39
MNN014 Mononeuritis 51 0.066
40
RNL006 Renal Glycosuria 49 0.066
41
EVN001 Evans' Syndrome 46 0.066
42
c JVN024 Juvenile Hereditary Hemochromatosis 45 0.066
43
AMN006 Aminoaciduria 44 0.066
44
P ATX010 Ataxia Neuropathy Spectrum 43 0.066
45
MLY001 Molybdenum Cofactor Deficiency 42 0.066
46
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 42 0.066
47
MCR225 Macrophage Activation Syndrome 40 0.066
48
BLR008 Bilirubin Metabolic Disorder 38 0.066
49
SYN053 Syndromic Diarrhea 34 0.066
50
c BNG076 Benign Exophthalmos Syndrome 22 0.066
51
AND005 Androgen Insensitivity Syndrome, Mild 21 0.066
52
OTP003 Oto-Palatal-Digital Syndrome 17 0.066
53
MLY005 Molybdenum Cofactor Deficiency B 14 0.066