Search results for TALDO1

72 hits were found for TALDO1

# Family MCID Name MIFTS Score
1
TRN021 Transaldolase Deficiency 43 50.026
2
LVR012 Liver Cirrhosis 63 16.334
3
P MLT020 Multiple Sclerosis 79 16.072
4
P CTR002 Cataract 60 15.632
5
P CTS001 Cutis Laxa 65 13.831
6
PNC001 Pancytopenia 53 13.137
7
c AMY091 Amyotrophic Lateral Sclerosis 1 88 12.035
8
SNL007 Senile Cataract 40 11.365
9
RBS005 Ribose 5-Phosphate Isomerase Deficiency 35 8.036
10
PYR022 Pyruvate Dehydrogenase E1-Alpha Deficiency 64 8.036
11
HYP827 Hypomagnesemia 5, Renal, with or Without Ocular Involvement 43 8.036
12
P LVR013 Liver Disease 69 3.388
13
P BRS047 Breast Cancer 98 1.990
14
HYD038 Hydrops Fetalis, Nonimmune 59 1.985
15
GLL048 Glial Tumor 52 1.985
16
CRB025 Carbohydrate Metabolic Disorder 40 1.985
17
GLM045 Glioma 63 1.985
18
PRT251 Proteinuria, Chronic Benign 57 1.772
19
P HMN010 Hemangioma 62 1.772
20
P ICH004 Ichthyosis 56 1.772
21
P MCR010 Microcephaly 60 1.713
22
P THR014 Thrombocytopenia 66 1.640
23
SQM013 Squamous Cell Carcinoma, Head and Neck 73 1.339
24
P HPT023 Hepatocellular Carcinoma 96 1.339
25
SQM006 Squamous Cell Carcinoma 60 1.339
26
SPL018 Splenomegaly 49 1.339
27
P HYP265 Hypotonia 42 1.339
28
P HYP077 Hypertrichosis 46 1.160
29
P NTR004 Neutropenia 63 1.160
30
c ATR087 Atrial Standstill 1 74 0.947
31
ANS021 Anisocoria 25 0.947
32
P INT070 Intestinal Obstruction 57 0.947
33
P HYP086 Hypothyroidism 69 0.947
34
P RSP003 Respiratory Failure 74 0.947
35
HYP056 Hypoglycemia 65 0.947
36
P OVR042 Ovarian Cancer 88 0.851
37
c INF194 Infantile Liver Failure Syndrome 29 0.825
38
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 60 0.739
39
c CLR087 Colorectal Cancer 12 34 0.739
40
GST103 Gastric Cancer, Hereditary Diffuse 68 0.739
41
SML009 Small Intestine Adenocarcinoma 57 0.739
42
P BLD134 Bladder Cancer 79 0.670
43
MNK001 Menkes Disease 64 0.670
44
c SYS001 Systemic Lupus Erythematosus 87 0.670
45
P CLR023 Colorectal Cancer 100 0.670
46
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 0.670
47
MTC108 Mitochondrial Short-Chain Enoyl-Coa Hydratase 1 Deficiency 32 0.670
48
MCS006 Macs Syndrome 58 0.670
49
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.670
50
P PRS040 Prostate Cancer 95 0.670
51
P MDL005 Medulloblastoma 75 0.670
52
P SCL018 Scoliosis 57 0.670
53
P LPS004 Lupus Erythematosus 61 0.670
54
P MVM001 Movement Disease 61 0.670
55
P HML002 Hemolytic Anemia 62 0.670
56
P ALP008 Alopecia 54 0.670
57
HYP066 Hyperglycemia 61 0.670
58
GLB002 Glioblastoma 67 0.670
59
ADN018 Adenoma 59 0.670
60
END086 End Stage Renal Disease 52 0.670
61
NPH009 Nephrolithiasis 54 0.670
62
c CTS032 Cutis Laxa, Autosomal Recessive, Type Iiib 37 0.670
63
P MLN007 Male Infertility 56 0.670
64
c SCN007 Secondary Hyperparathyroidism 51 0.670
65
OLG003 Oligohydramnios 51 0.670
66
P LTR001 Lateral Sclerosis 58 0.670
67
P HYP069 Hyperparathyroidism 62 0.670
68
c INH020 Inherited Metabolic Disorder 48 0.670
69
P INF032 Infertility 57 0.670
70
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.670
71
HYP080 Hypogonadism 50 0.670
72
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 0.670
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