Search results for "xanthinuria"

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

30 hits were found for 'xanthinuria'

# Family MCID Name MIFTS Score
1
P XNT005 Xanthinuria Type 1 44 9.372
2
c XNT006 Xanthinuria Type 2 16 7.857
3
MLY001 Molybdenum Cofactor Deficiency 42 0.152
4
LSC001 Lesch-Nyhan Syndrome 78 0.108
5
c DBT009 Diabetes Mellitus 73 0.108
6
P MTB001 Metabolic Syndrome X 69 0.108
7
c THY032 Thyroiditis 65 0.108
8
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 43 0.108
9
NTR005 Nutritional Deficiency Disease 33 0.108
10
AND002 Androgen Insensitivity Syndrome 80 0.076
11
c AXN002 Axenfeld-Rieger Syndrome 69 0.076
12
c AMY001 Amyotrophic Lateral Sclerosis 66 0.076
13
ACN002 Acanthosis Nigricans 64 0.076
14
c AMY077 Amyotrophic Lateral Sclerosis Type 18 63 0.076
15
c OCL002 Oculocutaneous Albinism 60 0.076
16
P AMY074 Amyotrophic Lateral Sclerosis Type 14 59 0.076
17
THR013 Thoracic Outlet Syndrome 52 0.076
18
MNN014 Mononeuritis 51 0.076
19
ALB002 Albinism 48 0.076
20
NPH003 Nephrocalcinosis 48 0.076
21
SLF004 Sulfite Oxidase Deficiency 47 0.076
22
P ATX010 Ataxia Neuropathy Spectrum 47 0.076
23
c JVN024 Juvenile Hereditary Hemochromatosis 44 0.076
24
MLY006 Molybdenum Cofactor Deficiency a 38 0.076
25
SYN053 Syndromic Diarrhea 34 0.076
26
c OCL036 Oculocutaneous Albinism Type 3 32 0.076
27
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 29 0.076
28
TFT003 Tufting Enteropathy 28 0.076
29
MLY005 Molybdenum Cofactor Deficiency B 18 0.076
30
OTP003 Oto-Palatal-Digital Syndrome 17 0.076