Search results for hypouricemia

56 hits were found for hypouricemia

# Family MCID Name MIFTS Score
1
P HYP761 Hypouricemia, Renal, 1 40 11.878
2
c HYP376 Hypouricemia, Renal, 2 19 5.816
3
c HYP799 Hypouricemia, Familial Renal, Due to Tubular Hypersecretion 9 2.682
4
HYP792 Hypouricemia, Hypercalcinuria, and Decreased Bone Density 9 2.682
5
HYP017 Hypophosphatemia 45 0.130
6
MLY009 Molybdenum Cofactor Deficiency, Complementation Group B 22 0.130
7
AGN016 Aging 65 0.113
8
NPH009 Nephrolithiasis 57 0.113
9
P FNC004 Fanconi Syndrome 54 0.113
10
PRN001 Purine Nucleoside Phosphorylase Deficiency 53 0.113
11
FNC060 Fanconi Renotubular Syndrome 4 with Maturity-Onset Diabetes of the Young 17 0.113
12
ALP046 Alport Syndrome, X-Linked 74 0.092
13
c CHR089 Chronic Kidney Failure 72 0.092
14
CHL065 Cholangiocarcinoma 70 0.092
15
P KDN018 Kidney Disease 69 0.092
16
ISC004 Ischemia 66 0.092
17
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.092
18
P PLY014 Polycystic Kidney Disease 60 0.092
19
P NPH012 Nephrotic Syndrome 60 0.092
20
GT001 Gout 60 0.092
21
P ENC018 Encephalopathy 58 0.092
22
c SVR001 Severe Acute Respiratory Syndrome 58 0.092
23
P HYP014 Hyperuricemia 54 0.092
24
FNC009 Fanconi-Bickel Syndrome 53 0.092
25
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.092
26
HYP005 Hypokalemia 53 0.092
27
NPH003 Nephrocalcinosis 49 0.092
28
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 44 0.092
29
IDP033 Idiopathic Edema 42 0.092
30
P XNT004 Xanthinuria 39 0.092
31
P HYP733 Hypercalciuria, Absorptive, 2 37 0.092
32
c XNT011 Xanthinuria, Type Ii 34 0.092
33
MLY008 Molybdenum Cofactor Deficiency, Complementation Group a 29 0.092
34
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 29 0.092
35
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.092
36
c LKM061 Leukemia, Acute Myeloid 81 0.065
37
P LKM002 Leukemia 75 0.065
38
P PNM007 Pneumonia 70 0.065
39
P MYL006 Myeloid Leukemia 69 0.065
40
P ANR048 Aniridia 1 68 0.065
41
GST045 Gastroenteritis 65 0.065
42
NPH091 Nephrolithiasis, Calcium Oxalate 51 0.065
43
END072 Endotheliitis 46 0.065
44
BLR008 Bilirubin Metabolic Disorder 45 0.065
45
MCR225 Macrophage Activation Syndrome 44 0.065
46
c XNT010 Xanthinuria, Type I 43 0.065
47
AMN006 Aminoaciduria 41 0.065
48
c HYP758 Hyperuricemic Nephropathy, Familial Juvenile, 1 40 0.065
49
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.065
50
MLY001 Molybdenum Cofactor Deficiency 37 0.065
51
SPN331 Spondyloocular Syndrome 34 0.065
52
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.065
53
ALR002 Al-Raqad Syndrome 30 0.065
54
ANR038 Anorexia Nervosa 1 21 0.065
55
MLY010 Molybdenum Cofactor Deficiency, Complementation Group C 21 0.065
56
BLD137 Blood Group--Ahonen 17 0.065
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