Search results for MUT

47 hits were found for MUT

# Family MCID Name MIFTS Score
1
MTH039 Methylmalonic Aciduria, Mut(0) Type 35 20.119
2
P MTH008 Methylmalonic Acidemia 56 17.787
3
c MTR038 Mut-Related Methylmalonic Acidemia 6 10.762
4
ISL099 Isolated Methylmalonic Acidemia 21 3.314
5
MTH025 Methylmalonyl-Coenzyme a Mutase Deficiency 8 3.280
6
ORG002 Organic Acidemia 38 3.240
7
CBL006 Cblf 20 3.240
8
PRP084 Propionicacidemia 57 3.193
9
AMN002 Amino Acid Metabolic Disorder 48 3.193
10
TRN022 Transcobalamin Ii Deficiency 47 3.193
11
VTM003 Vitamin Metabolic Disorder 31 3.193
12
MTH055 Methylmalonic Aciduria and Homocystinuria, Cbld Type 32 0.180
13
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 48 0.165
14
P CLR023 Colorectal Cancer 95 0.147
15
P MTH033 Methylmalonic Aciduria, Vitamin B12-Responsive 23 0.147
16
c MTH034 Methylmalonic Aciduria, Vitamin B12-Responsive, Due to Defect in Synthesis of Adenosylcobalamin, Cblb Complementation Type 22 0.147
17
SQM006 Squamous Cell Carcinoma 69 0.127
18
MTH056 Methylmalonic Aciduria and Homocystinuria, Cblf Type 32 0.127
19
P LNG032 Lung Cancer 94 0.104
20
MTH051 Methylmalonic Aciduria and Homocystinuria, Cblj Type 24 0.104
21
P BRS047 Breast Cancer 100 0.074
22
NRL016 Neural Tube Defects 76 0.074
23
CRH001 Crohn's Disease 73 0.074
24
P LKM002 Leukemia 72 0.074
25
P KDN018 Kidney Disease 65 0.074
26
P MYL006 Myeloid Leukemia 64 0.074
27
P ESP024 Esophagitis 59 0.074
28
HYP266 Hypoxia 55 0.074
29
P LRY019 Laryngitis 53 0.074
30
P PLY014 Polycystic Kidney Disease 52 0.074
31
RTN018 Retinal Disease 51 0.074
32
P HMC002 Homocystinuria 49 0.074
33
c CLL013 Cell Type Cancer 48 0.074
34
HPT074 Hepatic Adenoma, Somatic 44 0.074
35
c MCL060 Macular Dystrophy, Vitelliform, 3 40 0.074
36
HMC006 Homocystinuria Due to Mthfr Deficiency 40 0.074
37
FND002 Fundus Dystrophy 39 0.074
38
P HYP265 Hypotonia 39 0.074
39
LKP003 Leukoplakia 38 0.074
40
P VTL001 Vitelliform Macular Dystrophy 38 0.074
41
ADP007 Adie Pupil 35 0.074
42
PRP026 Peripheral Retinal Degeneration 34 0.074
43
CRN246 Cranioosteoarthropathy 33 0.074
44
ALR002 Al-Raqad Syndrome 29 0.074
45
HNM002 Hinman Syndrome 27 0.074
46
P BST001 Bestrophinopathy 26 0.074
47
AND005 Androgen Insensitivity Syndrome, Mild 16 0.074
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