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

31 hits were found for 'xanthinuria'

# ++ Fam MCID Name MIFTS Score
1
P XNT005 Xanthinuria Type 1 32 8.450
2
c XNT006 Xanthinuria Type 2 9 7.843
3
MLY001 Molybdenum Cofactor Deficiency 34 0.320
4
ALB002 Albinism 50 0.199
5
c OCL036 Oculocutaneous Albinism Type 3 22 0.185
6
TFT003 Tufting Enteropathy 26 0.168
7
c OCL002 Oculocutaneous Albinism 56 0.130
8
THR013 Thoracic Outlet Syndrome 53 0.130
9
MNN014 Mononeuritis 40 0.130
10
JVN024 Juvenile Hereditary Hemochromatosis 28 0.130
11
ACN002 Acanthosis Nigricans 70 0.107
12
LSC001 Lesch-Nyhan Syndrome 68 0.107
13
NSY001 N Syndrome 57 0.107
14
P THR090 Thrombocythemia 1 48 0.107
15
P DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 23 0.107
16
MLY007 Molybdenum Cofactor Deficiency C 16 0.107
17
RFS004 Rufous Oculocutaneous Albinism 9 0.107
18
P AMY001 Amyotrophic Lateral Sclerosis 87 0.075
19
P WSK001 Wiskott-Aldrich Syndrome 76 0.075
20
AND002 Androgen Insensitivity Syndrome 75 0.075
21
c DBT009 Diabetes Mellitus 68 0.075
22
WST001 West Syndrome 64 0.075
23
c THY032 Thyroiditis 61 0.075
24
c AXN002 Axenfeld-Rieger Syndrome 57 0.075
25
NPH003 Nephrocalcinosis 52 0.075
26
ADN024 Adenine Phosphoribosyltransferase Deficiency 42 0.075
27
SLF004 Sulfite Oxidase Deficiency 34 0.075
28
c ATX010 Ataxia Neuropathy Spectrum 33 0.075
29
MLY006 Molybdenum Cofactor Deficiency a 32 0.075
30
P ISC010 Isochromosome Yp 14 0.075
31
OTP003 Oto-Palatal-Digital Syndrome 13 0.075