Search results for "hypouricemia"

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

57 hits were found for 'hypouricemia'

# Family MCID Name MIFTS Score
1
P RNL042 Renal Hypouricemia 37 8.339
2
c RNL053 Renal Hypouricemia 2 12 5.247
3
c RNL052 Renal Hypouricemia 1 7 3.710
4
HYP017 Hypophosphatemia 48 0.129
5
P FNC004 Fanconi Syndrome 50 0.112
6
CHL065 Cholangiocarcinoma 69 0.091
7
c NPH012 Nephrotic Syndrome 67 0.091
8
P GT001 Gout 65 0.091
9
ISC004 Ischemia 62 0.091
10
P NPH009 Nephrolithiasis 59 0.091
11
c SVR001 Severe Acute Respiratory Syndrome 58 0.091
12
PRN001 Purine Nucleoside Phosphorylase Deficiency 58 0.091
13
P HYP014 Hyperuricemia 55 0.091
14
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 50 0.091
15
HYP005 Hypokalemia 49 0.091
16
IDP033 Idiopathic Edema 32 0.091
17
MLY005 Molybdenum Cofactor Deficiency B 18 0.091
18
P ACT019 Acute Myeloid Leukemia 92 0.064
19
P LVR011 Liver Cancer 90 0.064
20
P ATX002 Ataxia Telangiectasia 87 0.064
21
AND002 Androgen Insensitivity Syndrome 80 0.064
22
P PNM007 Pneumonia 77 0.064
23
P LKM002 Leukemia 76 0.064
24
c MYL006 Myeloid Leukemia 74 0.064
25
c DBT009 Diabetes Mellitus 73 0.064
26
c PRM002 Primary Hyperoxaluria 73 0.064
27
c AXN002 Axenfeld-Rieger Syndrome 69 0.064
28
P MTB001 Metabolic Syndrome X 69 0.064
29
c AMY001 Amyotrophic Lateral Sclerosis 66 0.064
30
ACN002 Acanthosis Nigricans 64 0.064
31
c AMY077 Amyotrophic Lateral Sclerosis Type 18 63 0.064
32
P AMY074 Amyotrophic Lateral Sclerosis Type 14 59 0.064
33
MYC002 Mycobacterium Avium Complex Disease 58 0.064
34
BRN029 Brain Disease 57 0.064
35
ART001 Arterial Tortuosity Syndrome 55 0.064
36
P PND001 Pain Disorder 54 0.064
37
c ACR001 Aicardi-Goutieres Syndrome 54 0.064
38
AND003 Andersen-Tawil Syndrome 53 0.064
39
THR013 Thoracic Outlet Syndrome 52 0.064
40
RNL006 Renal Glycosuria 51 0.064
41
MNN014 Mononeuritis 51 0.064
42
FNC040 Fanconi Bickel Syndrome 51 0.064
43
P ATX010 Ataxia Neuropathy Spectrum 47 0.064
44
EVN001 Evans' Syndrome 45 0.064
45
c JVN024 Juvenile Hereditary Hemochromatosis 44 0.064
46
AMN006 Aminoaciduria 43 0.064
47
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 43 0.064
48
MLY001 Molybdenum Cofactor Deficiency 42 0.064
49
MCR225 Macrophage Activation Syndrome 39 0.064
50
MLY006 Molybdenum Cofactor Deficiency a 38 0.064
51
BLR008 Bilirubin Metabolic Disorder 37 0.064
52
SYN053 Syndromic Diarrhea 34 0.064
53
IMM033 Immunodeficiency Due to Purine Nucleoside Phosphorylase Deficiency 25 0.064
54
c BNG076 Benign Exophthalmos Syndrome 22 0.064
55
AND005 Androgen Insensitivity Syndrome, Mild 21 0.064
56
OTP003 Oto-Palatal-Digital Syndrome 17 0.064
57
URC009 Uric Acid Concentration, Serum, Qtl 2 9 0.064