Search results for g6pd

131 hits were found for g6pd

# Family MCID Name MIFTS Score
1
HML006 Hemolytic Anemia Due to G6pd Deficiency 33 19.141
2
GLC009 Glucosephosphate Dehydrogenase Deficiency 41 17.163
3
MLR004 Malaria 83 11.464
4
FVS001 Favism 40 5.116
5
P HML002 Hemolytic Anemia 62 4.556
6
DFC004 Deficiency Anemia 64 4.017
7
NNT012 Neonatal Jaundice 50 3.947
8
PLS006 Plasmodium Vivax Malaria 53 3.932
9
c CNG027 Congenital Hemolytic Anemia 48 3.618
10
P MTH007 Methemoglobinemia 45 3.559
11
P THL005 Thalassemia 64 3.527
12
PLS007 Plasmodium Falciparum Malaria 55 3.491
13
SCK005 Sickle Cell Disease 51 3.491
14
P KRN004 Kernicterus 46 3.472
15
PYR013 Pyruvate Kinase Deficiency 58 3.451
16
SCK003 Sickle Cell Anemia 71 3.429
17
SNL007 Senile Cataract 37 3.429
18
ACN011 Acne 62 3.405
19
GLB001 Gilbert Syndrome 60 3.405
20
PHN003 Phenylketonuria 72 3.379
21
P CLR019 Color Blindness 46 3.379
22
MCR018 Microcytic Anemia 43 3.379
23
BLC004 Blackwater Fever 32 3.379
24
c ACQ047 Acquired Methemoglobinemia 23 3.379
25
c G6P002 G6pd-Related Altered Drug Metabolism 7 3.121
26
CNG017 Congenital Nonspherocytic Hemolytic Anemia 29 3.049
27
c CNG223 Congenital Methemoglobinemia 28 2.983
28
CHR012 Chronic Granulomatous Disease 65 2.926
29
GLC006 Galactosemia 64 2.926
30
THL016 Thalassemias, Alpha- 53 2.926
31
LYM019 Lymphosarcoma 53 2.926
32
HYP141 Hyperphenylalaninemia 49 2.926
33
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 46 2.926
34
MNN020 Meningococcal Infection 43 2.926
35
GLT007 Glutathione Synthetase Deficiency 43 2.926
36
PRT026 Parotitis 42 2.926
37
BLR008 Bilirubin Metabolic Disorder 42 2.926
38
KR001 Koro 32 2.926
39
BLD052 Blood Group Incompatibility 27 2.926
40
GLC039 Glucosephosphate Isomerase Deficiency 19 2.926
41
6PH001 6-Phosphogluconate Dehydrogenase Deficiency 17 2.926
42
MNT017 Mental Retardation Hip Luxation G6pd Variant 2 2.886
43
BCK006 Back Pain 43 2.425
44
P HRD011 Hereditary Spherocytosis 54 1.736
45
NTR005 Nutritional Deficiency Disease 36 0.203
46
c INH020 Inherited Metabolic Disorder 49 0.178
47
CRB025 Carbohydrate Metabolic Disorder 46 0.178
48
P HPT021 Hepatitis 69 0.138
49
P CTR002 Cataract 58 0.113
50
P EXN002 Exanthem 57 0.113
51
HMG005 Hemoglobinopathy 52 0.113
52
PRS036 Parasitic Protozoa Infectious Disease 41 0.113
53
P LKM002 Leukemia 71 0.080
54
c HPT007 Hepatitis E 54 0.080
55
P CNG003 Congenital Dyserythropoietic Anemia 40 0.080
56
FLC001 Folic Acid Deficiency Anemia 34 0.080
57
HPL001 Hip Luxation 17 0.080
58
P HPT023 Hepatocellular Carcinoma 92 0.056
59
P OBS005 Obesity 92 0.056
60
P RHM011 Rheumatoid Arthritis 89 0.056
61
HV1006 Hiv-1 80 0.056
62
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.056
63
GST053 Gastric Cancer 78 0.056
64
P ART022 Arthritis 75 0.056
65
KWS002 Kawasaki Disease 70 0.056
66
SQM006 Squamous Cell Carcinoma 70 0.056
67
P DMN001 Diamond-Blackfan Anemia 69 0.056
68
FBR012 Fabry Disease 69 0.056
69
c HPT001 Hepatitis C 68 0.056
70
SKN016 Skin Disease 66 0.056
71
BRC012 Brucellosis 66 0.056
72
P DYS154 Dystonia 65 0.056
73
c HPT016 Hepatitis B 64 0.056
74
P OST001 Osteopetrosis 63 0.056
75
MLN008 Melanoma 62 0.056
76
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 62 0.056
77
P ESP024 Esophagitis 61 0.056
78
TYP007 Typhoid Fever 61 0.056
79
CRY002 Cryptorchidism 60 0.056
80
c VRL010 Viral Hepatitis 60 0.056
81
c HPT003 Hepatitis a 59 0.056
82
P NRP001 Neuropathy 59 0.056
83
CHL068 Cholestasis 59 0.056
84
ADL030 Adult-Onset Still's Disease 59 0.056
85
LPD008 Lipid Metabolism Disorder 58 0.056
86
ETN001 Eating Disorder 58 0.056
87
KND001 Kindler Syndrome 57 0.056
88
CTS003 Coats Disease 57 0.056
89
RHB003 Rhabdomyosarcoma 57 0.056
90
ADM013 Adamantinoma of Long Bones 57 0.056
91
P ACT074 Acute Lymphocytic Leukemia 56 0.056
92
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.056
93
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 53 0.056
94
KRT002 Keratomalacia 52 0.056
95
SLM003 Salmonellosis 52 0.056
96
KLD001 Keloids 51 0.056
97
STM006 Stomach Disease 50 0.056
98
THR013 Thoracic Outlet Syndrome 50 0.056
99
OVR063 Overnutrition 50 0.056
100
HMG002 Hemoglobinuria 48 0.056
101
c HMG001 Hemoglobin C Disease 47 0.056
102
VND001 Vein Disease 47 0.056
103
PRP007 Priapism 46 0.056
104
RNL078 Renal Dysplasia 45 0.056
105
VTM002 Vitamin B12 Deficiency 44 0.056
106
c HMG003 Hemoglobin E Disease 44 0.056
107
HYD012 Hydrops Fetalis 43 0.056
108
PLS016 Plasma Cell Leukemia 42 0.056
109
c HRD012 Hereditary Elliptocytosis 42 0.056
110
HMT018 Hematopoietic Stem Cell Transplantation 41 0.056
111
TNP003 Tn Polyagglutination Syndrome, Somatic 41 0.056
112
CRB009 Cerebritis 39 0.056
113
THL010 Thalassemia Minor 39 0.056
114
P CHR342 Chiari Malformation 38 0.056
115
ISC002 Ischemic Optic Neuropathy 37 0.056
116
CPL005 Capillary Disease 36 0.056
117
ALR002 Al-Raqad Syndrome 36 0.056
118
ANG049 Angioedema Induced by Ace Inhibitors 34 0.056
119
SBC017 Sebaceous Gland Disease 34 0.056
120
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 33 0.056
121
DBT007 Diabetic Cataract 32 0.056
122
VTM003 Vitamin Metabolic Disorder 30 0.056
123
c TRC078 Trichohepatoenteric Syndrome 2 29 0.056
124
GLC081 Glucose Phosphate Isomerase Deficiency 24 0.056
125
MXD019 Mixed Malaria 23 0.056
126
ANM012 Anemia, Hemolytic, Due to Umph1 Deficiency 20 0.056
127
PYR009 Pyridoxine Deficiency Anemia 18 0.056
128
LCT008 Lactate Dehydrogenase Deficiency 17 0.056
129
TRT015 Torticollis, Keloids, Cryptorchidism, and Renal Dysplasia 16 0.056
130
c BCT003 Bacterial Exanthem 11 0.056
131
FBR090 Fibro-Adipose Vascular Anomaly 10 0.056
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