Search results for g6pd

117 hits were found for g6pd

# Family MCID Name MIFTS Score
1
HML006 Hemolytic Anemia Due to G6pd Deficiency 34 18.033
2
GLC009 Glucosephosphate Dehydrogenase Deficiency 41 17.843
3
MLR004 Malaria 82 12.033
4
FVS001 Favism 40 5.150
5
P HML002 Hemolytic Anemia 61 4.510
6
NNT012 Neonatal Jaundice 47 3.581
7
PLS006 Plasmodium Vivax Malaria 52 3.564
8
DFC004 Deficiency Anemia 60 3.469
9
c CNG027 Congenital Hemolytic Anemia 45 3.469
10
c G6P002 G6pd-Related Altered Drug Metabolism 7 3.158
11
P MTH007 Methemoglobinemia 44 3.141
12
PLS007 Plasmodium Falciparum Malaria 54 3.067
13
SCK005 Sickle Cell Disease 51 3.067
14
P KRN004 Kernicterus 45 3.067
15
PYR013 Pyruvate Kinase Deficiency 58 3.022
16
SNL007 Senile Cataract 37 2.997
17
ACN011 Acne 59 2.970
18
GLB001 Gilbert Syndrome 56 2.970
19
PHN003 Phenylketonuria 72 2.938
20
P CLR019 Color Blindness 45 2.938
21
MCR018 Microcytic Anemia 44 2.938
22
BLC004 Blackwater Fever 31 2.938
23
c ACQ047 Acquired Methemoglobinemia 23 2.938
24
MNT017 Mental Retardation Hip Luxation G6pd Variant 2 2.897
25
CNG017 Congenital Nonspherocytic Hemolytic Anemia 28 2.543
26
ISC002 Ischemic Optic Neuropathy 44 2.436
27
BCK006 Back Pain 41 2.436
28
CHR012 Chronic Granulomatous Disease 66 2.399
29
GLC006 Galactosemia 66 2.399
30
THL013 Thalassemia, Hispanic Gamma-Delta-Beta 58 2.399
31
THL016 Thalassemias, Alpha- 53 2.399
32
LYM019 Lymphosarcoma 53 2.399
33
HYP141 Hyperphenylalaninemia 48 2.399
34
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 46 2.399
35
BLR008 Bilirubin Metabolic Disorder 44 2.399
36
GLT007 Glutathione Synthetase Deficiency 43 2.399
37
MNN020 Meningococcal Infection 42 2.399
38
PRT026 Parotitis 42 2.399
39
KR001 Koro 32 2.399
40
c CNG223 Congenital Methemoglobinemia 26 2.399
41
BLD052 Blood Group Incompatibility 25 2.399
42
GLC039 Glucosephosphate Isomerase Deficiency 19 2.399
43
6PH001 6-Phosphogluconate Dehydrogenase Deficiency 16 2.399
44
P HRD011 Hereditary Spherocytosis 53 1.745
45
P HPT021 Hepatitis 68 0.155
46
P THL005 Thalassemia 61 0.155
47
BRT030 Birth Defects 44 0.143
48
LCT007 Lactate Dehydrogenase a Deficiency 23 0.143
49
LCT008 Lactate Dehydrogenase Deficiency 16 0.143
50
P CTR002 Cataract 57 0.117
51
P EXN002 Exanthem 57 0.117
52
HMG005 Hemoglobinopathy 51 0.117
53
PRS036 Parasitic Protozoa Infectious Disease 42 0.101
54
P LKM002 Leukemia 72 0.083
55
c HPT003 Hepatitis a 56 0.083
56
c HPT007 Hepatitis E 51 0.083
57
PHY002 Physical Disorder 43 0.083
58
P CNG003 Congenital Dyserythropoietic Anemia 39 0.083
59
HPL001 Hip Luxation 17 0.083
60
P OBS005 Obesity 91 0.059
61
P HPT023 Hepatocellular Carcinoma 89 0.059
62
P RHM011 Rheumatoid Arthritis 87 0.059
63
HV1006 Hiv-1 80 0.059
64
P ART022 Arthritis 72 0.059
65
SCK003 Sickle Cell Anemia 71 0.059
66
FBR012 Fabry Disease 71 0.059
67
MLN008 Melanoma 70 0.059
68
P DMN001 Diamond-Blackfan Anemia 70 0.059
69
SQM006 Squamous Cell Carcinoma 69 0.059
70
KWS002 Kawasaki Disease 67 0.059
71
P OST001 Osteopetrosis 63 0.059
72
c HPT001 Hepatitis C 62 0.059
73
c HPT016 Hepatitis B 62 0.059
74
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 62 0.059
75
CRY002 Cryptorchidism 61 0.059
76
BRC012 Brucellosis 61 0.059
77
TYP007 Typhoid Fever 61 0.059
78
P DYS154 Dystonia 61 0.059
79
ADL030 Adult-Onset Still's Disease 60 0.059
80
ISC004 Ischemia 59 0.059
81
P ESP024 Esophagitis 59 0.059
82
RHB003 Rhabdomyosarcoma 58 0.059
83
CHL068 Cholestasis 58 0.059
84
c VRL010 Viral Hepatitis 58 0.059
85
P NRP001 Neuropathy 57 0.059
86
P BDD001 Budd-Chiari Syndrome 56 0.059
87
P ACT074 Acute Lymphocytic Leukemia 55 0.059
88
KLD001 Keloids 52 0.059
89
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 52 0.059
90
SLM003 Salmonellosis 51 0.059
91
RNL078 Renal Dysplasia 50 0.059
92
VND001 Vein Disease 49 0.059
93
THR013 Thoracic Outlet Syndrome 49 0.059
94
OVR063 Overnutrition 48 0.059
95
HMG002 Hemoglobinuria 48 0.059
96
P CRV039 Cervicitis 45 0.059
97
PRP007 Priapism 45 0.059
98
c HMG001 Hemoglobin C Disease 44 0.059
99
HYD012 Hydrops Fetalis 43 0.059
100
P HYP729 Hypersensitivity Reaction Disease 43 0.059
101
c HMG003 Hemoglobin E Disease 43 0.059
102
PLS016 Plasma Cell Leukemia 41 0.059
103
c HRD012 Hereditary Elliptocytosis 41 0.059
104
BRN080 Brain Ischemia 40 0.059
105
HMT018 Hematopoietic Stem Cell Transplantation 40 0.059
106
CRB009 Cerebritis 39 0.059
107
THL010 Thalassemia Minor 38 0.059
108
P CHR342 Chiari Malformation 38 0.059
109
DBT007 Diabetic Cataract 37 0.059
110
SBC017 Sebaceous Gland Disease 34 0.059
111
c TRC078 Trichohepatoenteric Syndrome 2 34 0.059
112
ALR002 Al-Raqad Syndrome 29 0.059
113
ANM026 Anemia, X-Linked, with/without Neutropenia and/or Platelet Abnormalities 25 0.059
114
MXD019 Mixed Malaria 22 0.059
115
ANM012 Anemia, Hemolytic, Due to Umph1 Deficiency 20 0.059
116
TRT015 Torticollis, Keloids, Cryptorchidism, and Renal Dysplasia 18 0.059
117
FBR090 Fibro-Adipose Vascular Anomaly 10 0.059
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