Search results for "xanthinuria"

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

28 hits were found for 'xanthinuria'

# Family MCID Name MIFTS Score
1
P XNT005 Xanthinuria Type 1 43 9.366
2
c XNT006 Xanthinuria Type 2 16 7.865
3
MLY001 Molybdenum Cofactor Deficiency 42 0.155
4
LSC001 Lesch-Nyhan Syndrome 78 0.110
5
c DBT009 Diabetes Mellitus 74 0.110
6
P MTB001 Metabolic Syndrome X 70 0.110
7
c THY032 Thyroiditis 66 0.110
8
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 42 0.110
9
NTR005 Nutritional Deficiency Disease 33 0.110
10
AND002 Androgen Insensitivity Syndrome 80 0.078
11
c AXN002 Axenfeld-Rieger Syndrome 67 0.078
12
c AMY001 Amyotrophic Lateral Sclerosis 67 0.078
13
ACN002 Acanthosis Nigricans 63 0.078
14
c AMY077 Amyotrophic Lateral Sclerosis Type 18 60 0.078
15
P AMY074 Amyotrophic Lateral Sclerosis Type 14 56 0.078
16
c OCL002 Oculocutaneous Albinism 56 0.078
17
THR013 Thoracic Outlet Syndrome 52 0.078
18
MNN014 Mononeuritis 51 0.078
19
ALB002 Albinism 49 0.078
20
NPH003 Nephrocalcinosis 49 0.078
21
c JVN024 Juvenile Hereditary Hemochromatosis 45 0.078
22
SLF004 Sulfite Oxidase Deficiency 44 0.078
23
P ATX010 Ataxia Neuropathy Spectrum 43 0.078
24
SYN053 Syndromic Diarrhea 34 0.078
25
c OCL036 Oculocutaneous Albinism Type 3 31 0.078
26
TFT003 Tufting Enteropathy 28 0.078
27
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.078
28
OTP003 Oto-Palatal-Digital Syndrome 17 0.078