Search results for "hypouricemia"

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

59 hits were found for 'hypouricemia'

# Family MCID Name MIFTS Score
1
P HYP612 Hypouricemia, Renal 34 11.238
2
c HYP376 Hypouricemia, Renal, 2 22 6.314
3
HYP017 Hypophosphatemia 39 0.127
4
P NPH009 Nephrolithiasis 48 0.110
5
MLY005 Molybdenum Cofactor Deficiency B 21 0.110
6
c AMY091 Amyotrophic Lateral Sclerosis 1 83 0.090
7
P ATX030 Ataxia-Telangiectasia 76 0.090
8
c SPN225 Spondyloarthropathy 1 66 0.090
9
P ANG001 Angelman Syndrome 66 0.090
10
P PRM002 Primary Hyperoxaluria 64 0.090
11
P HRM001 Hermansky-Pudlak Syndrome 62 0.090
12
c CHR089 Chronic Kidney Failure 61 0.090
13
c PNC108 Pancreatitis, Hereditary 59 0.090
14
P HMP002 Hemophagocytic Lymphohistiocytosis 59 0.090
15
ART001 Arterial Tortuosity Syndrome 59 0.090
16
P AND016 Andersen Syndrome 58 0.090
17
HNT002 Hantavirus Pulmonary Syndrome 52 0.090
18
P GT001 Gout 51 0.090
19
THR013 Thoracic Outlet Syndrome 47 0.090
20
P FNC004 Fanconi Syndrome 46 0.090
21
c ART101 Aortic Valve Disease 2 46 0.090
22
MYC002 Mycobacterium Avium Complex Disease 46 0.090
23
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 46 0.090
24
P HYP014 Hyperuricemia 45 0.090
25
P TRC086 Trichohepatoenteric Syndrome 1 42 0.090
26
HYP005 Hypokalemia 39 0.090
27
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 38 0.090
28
P XNT004 Xanthinuria 35 0.090
29
c BNG076 Benign Exophthalmos Syndrome 21 0.090
30
AND005 Androgen Insensitivity Syndrome, Mild 19 0.090
31
FNC051 Fanconi Renotubular Syndrome 4, with Maturity-Onset Diabetes of the Young 17 0.090
32
ANR002 Aniridia 72 0.063
33
P LKM002 Leukemia 61 0.063
34
P MYL006 Myeloid Leukemia 59 0.063
35
P PNM007 Pneumonia 56 0.063
36
CHL065 Cholangiocarcinoma 56 0.063
37
ACN002 Acanthosis Nigricans 53 0.063
38
P NPH012 Nephrotic Syndrome 52 0.063
39
c SVR001 Severe Acute Respiratory Syndrome 52 0.063
40
SCH016 Schimke Immunoosseous Dysplasia 51 0.063
41
FNC009 Fanconi-Bickel Syndrome 50 0.063
42
ISC004 Ischemia 47 0.063
43
GST045 Gastroenteritis 45 0.063
44
IMM033 Immunodeficiency Due to Purine Nucleoside Phosphorylase Deficiency 44 0.063
45
P ENC018 Encephalopathy 42 0.063
46
MNN014 Mononeuritis 39 0.063
47
TTR016 Tetra-Amelia Syndrome 38 0.063
48
P HYP623 Hyperuricemic Nephropathy, Familial Juvenile 1 37 0.063
49
c XNT010 Xanthinuria, Type I 36 0.063
50
IDP033 Idiopathic Edema 36 0.063
51
MLY001 Molybdenum Cofactor Deficiency 36 0.063
52
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 34 0.063
53
MLY006 Molybdenum Cofactor Deficiency a 33 0.063
54
AMN006 Aminoaciduria 32 0.063
55
MCR225 Macrophage Activation Syndrome 32 0.063
56
P ATX010 Ataxia Neuropathy Spectrum 31 0.063
57
SPN331 Spondyloocular Syndrome 30 0.063
58
ACT043 Acute Urate Nephropathy 30 0.063
59
NPH078 Nephrolithiasis, Uric Acid 16 0.063