Search results for hereditary persistence of fetal hemoglobin - sickle cell disease

69 hits were found for hereditary persistence of fetal hemoglobin - sickle cell disease

# Family MCID Name MIFTS Score
1
P LNG032 Lung Cancer 99 0.431
2
PRS047 Prostatitis 59 0.408
3
P PNC044 Pancreatitis 64 0.403
4
P ADN016 Adenocarcinoma 71 0.376
5
NRN002 Neuronitis 43 0.374
6
P PRS040 Prostate Cancer 88 0.347
7
P CLR023 Colorectal Cancer 98 0.327
8
MLN008 Melanoma 72 0.303
9
GST053 Gastric Cancer 84 0.275
10
P NRB001 Neuroblastoma 73 0.261
11
P ALZ034 Alzheimer Disease 95 0.234
12
P LYM026 Lymphoblastic Leukemia 66 0.228
13
ADN018 Adenoma 63 0.208
14
GLB002 Glioblastoma 74 0.188
15
GST050 Gastrointestinal System Disease 66 0.178
16
P HMR003 Hemorrhagic Disease 61 0.177
17
HYP056 Hypoglycemia 62 0.174
18
P ATR011 Atrial Fibrillation 68 0.170
19
P CTR002 Cataract 60 0.169
20
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 53 0.166
21
P HYP086 Hypothyroidism 62 0.159
22
CLT003 Colitis 63 0.156
23
P RNG031 Ring Chromosome Y Syndrome 29 0.148
24
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.134
25
MTH009 Mouth Disease 64 0.131
26
P END044 Endometriosis 71 0.128
27
MDS022 Mediastinitis 44 0.125
28
P CNJ013 Conjunctivitis 67 0.124
29
HYD059 Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect 34 0.124
30
c MCL042 Macular Degeneration, Age-Related, 1 79 0.124
31
P CLC063 Celiac Disease 1 65 0.116
32
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.116
33
P PLY011 Polycystic Ovary Syndrome 65 0.104
34
CHR005 Chorioamnionitis 52 0.101
35
LMB062 Limb Ischemia 52 0.099
36
PLM175 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 48 0.098
37
HDN002 Head Injury 48 0.094
38
LPD008 Lipid Metabolism Disorder 59 0.092
39
c ACT210 Acute Respiratory Distress Syndrome 63 0.085
40
PRT011 Protein C Deficiency 48 0.085
41
P ESS003 Essential Thrombocythemia 71 0.084
42
P STR035 Streptococcal Group a Invasive Disease 28 0.083
43
P FNC027 Fanconi Anemia, Complementation Group a 78 0.083
44
GRW007 Growth Hormone Deficiency 52 0.078
45
CYN002 Cyanosis, Transient Neonatal 32 0.078
46
WLS001 Wilson Disease 72 0.076
47
c ART101 Aortic Valve Disease 2 65 0.076
48
BLD053 Blood Platelet Disease 45 0.075
49
HLL004 Hellp Syndrome 53 0.072
50
ADN001 Adenosine Deaminase Deficiency 52 0.071
51
P LCT001 Lactic Acidosis 51 0.069
52
SCN001 Secondary Hyperparathyroidism of Renal Origin 40 0.068
53
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.067
54
GGN002 Gigantism 36 0.067
55
c PRG042 Progressive Familial Heart Block, Type Ia 57 0.067
56
DSS009 Disseminated Intravascular Coagulation 56 0.066
57
STR020 Strabismus 55 0.065
58
P HYP750 Hypertriglyceridemia, Familial 55 0.064
59
PPL059 Popliteal Pterygium Syndrome, Lethal Type 37 0.063
60
THR035 Thrombasthenia 46 0.061
61
c FTL035 Fetal Hemoglobin Quantitative Trait Locus 3 14 0.059
62
TWN001 Twin-to-Twin Transfusion Syndrome 51 0.058
63
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 58 0.054
64
CHR178 Chromosomal Triplication 35 0.054
65
FNT004 Fainting 36 0.047
66
c DMN023 Diamond-Blackfan Anemia 1 48 0.044
67
ESN011 Eisenmenger Syndrome 49 0.042
68
c HYP057 Hypervitaminosis D 40 0.041
69
MDL009 Medullary Sponge Kidney 46 0.040
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