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

32 hits were found for 'xanthinuria'

# Family MCID Name MIFTS Score
1
P XNT005 Xanthinuria Type 1 39 8.441
2
c XNT006 Xanthinuria Type 2 15 7.835
3
MLY001 Molybdenum Cofactor Deficiency 31 0.299
4
ALB002 Albinism 50 0.198
5
c OCL036 Oculocutaneous Albinism Type 3 29 0.183
6
TFT003 Tufting Enteropathy 21 0.167
7
c OCL002 Oculocutaneous Albinism 60 0.129
8
THR013 Thoracic Outlet Syndrome 54 0.129
9
MNN014 Mononeuritis 48 0.129
10
P JVN024 Juvenile Hereditary Hemochromatosis 35 0.129
11
LSC001 Lesch-Nyhan Syndrome 79 0.106
12
ACN002 Acanthosis Nigricans 73 0.106
13
P MTB001 Metabolic Syndrome X 67 0.106
14
P THR090 Thrombocythemia 1 54 0.106
15
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.106
16
NTR005 Nutritional Deficiency Disease 28 0.106
17
RFS004 Rufous Oculocutaneous Albinism 8 0.106
18
P AMY001 Amyotrophic Lateral Sclerosis 100 0.075
19
AND002 Androgen Insensitivity Syndrome 88 0.075
20
P WSK001 Wiskott-Aldrich Syndrome 87 0.075
21
c DBT009 Diabetes Mellitus 80 0.075
22
c TYP008 Type 1 Diabetes Mellitus 77 0.075
23
c THY032 Thyroiditis 67 0.075
24
WST001 West Syndrome 64 0.075
25
c AXN002 Axenfeld-Rieger Syndrome 60 0.075
26
NPH003 Nephrocalcinosis 53 0.075
27
ADN024 Adenine Phosphoribosyltransferase Deficiency 52 0.075
28
P ATX010 Ataxia Neuropathy Spectrum 44 0.075
29
SYN053 Syndromic Diarrhea 42 0.075
30
SLF004 Sulfite Oxidase Deficiency 39 0.075
31
P ISC010 Isochromosome Yp 14 0.075
32
OTP003 Oto-Palatal-Digital Syndrome 13 0.075