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

The MalaCard for "hereditary persistence of fetal hemoglobin - sickle cell disease" has been retired.
Searching MalaCards for entries containing "hereditary persistence of fetal hemoglobin - sickle cell disease"

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

# Family MCID Name MIFTS Score
1
P LNG032 Lung Cancer 92 0.393
2
PRS047 Prostatitis 56 0.392
3
P PNC044 Pancreatitis 62 0.384
4
NRN002 Neuronitis 40 0.364
5
P ADN016 Adenocarcinoma 69 0.344
6
P PRS040 Prostate Cancer 89 0.338
7
P CLR023 Colorectal Cancer 96 0.317
8
MLN008 Melanoma 61 0.288
9
P OVR042 Ovarian Cancer 73 0.286
10
P NRB001 Neuroblastoma 70 0.259
11
GST053 Gastric Cancer 52 0.240
12
P LYM026 Lymphoblastic Leukemia 60 0.218
13
ADN018 Adenoma 59 0.202
14
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.167
15
HYP056 Hypoglycemia 60 0.165
16
P CTR002 Cataract 57 0.158
17
P ATR011 Atrial Fibrillation 63 0.157
18
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.156
19
ACQ007 Acquired Immunodeficiency Syndrome 60 0.149
20
CLT003 Colitis 56 0.145
21
P UTR038 Uterine Disease 38 0.145
22
P SKN013 Skin Benign Neoplasm 38 0.144
23
P HYP086 Hypothyroidism 63 0.141
24
BRS051 Breast Disease 57 0.140
25
TTH006 Tooth Disease 52 0.140
26
P LFR001 Li-Fraumeni Syndrome 79 0.138
27
IMM102 Immunodeficiency 14 33 0.135
28
P END044 Endometriosis 53 0.122
29
P CNJ013 Conjunctivitis 65 0.122
30
BRN106 Burns 52 0.118
31
HYD012 Hydrops Fetalis 45 0.118
32
RNL101 Renal Cell Carcinoma, Papillary 63 0.117
33
MDS022 Mediastinitis 37 0.114
34
P CLC005 Celiac Disease 67 0.113
35
EPD016 Epidermolysis Bullosa 59 0.113
36
FML037 Female Breast Cancer 49 0.110
37
GTR002 Goiter 54 0.108
38
CHR005 Chorioamnionitis 47 0.105
39
SPN051 Spondylitis 50 0.102
40
LMB062 Limb Ischemia 48 0.100
41
ATM014 Autoimmune Disease of Endocrine System 37 0.099
42
P HYP076 Hyperthyroidism 59 0.099
43
P HMR012 Hemorrhagic Fever 55 0.098
44
P PLY011 Polycystic Ovary Syndrome 64 0.095
45
GLC003 Glucose Intolerance 56 0.089
46
ALC007 Alcohol Dependence 66 0.089
47
GRW007 Growth Hormone Deficiency 49 0.084
48
P ESS003 Essential Thrombocythemia 66 0.083
49
THY030 Thyroid Gland Disease 52 0.083
50
TXC005 Toxic Shock Syndrome 61 0.081
51
CRN030 Coronary Stenosis 50 0.080
52
DCH001 Duchenne Muscular Dystrophy 81 0.077
53
P FML035 Familial Hyperlipidemia 49 0.070
54
ORL014 Oral Pharyngeal Disorders 13 0.070
55
CRN036 Craniopharyngioma 54 0.068
56
HLL004 Hellp Syndrome 48 0.067
57
P LCT001 Lactic Acidosis 52 0.066
58
ADN001 Adenosine Deaminase Deficiency 45 0.064
59
GLC006 Galactosemia 64 0.062
60
PRT082 Preterm Premature Rupture of the Membranes 46 0.062
61
GGN002 Gigantism 29 0.062
62
TWN001 Twin-to-Twin Transfusion Syndrome 47 0.059
63
P EPD002 Epidermolytic Hyperkeratosis 51 0.055
64
P PCH001 Pachyonychia Congenita 54 0.054
65
FNT004 Fainting 33 0.048
66
AMN006 Aminoaciduria 39 0.046
67
MDL009 Medullary Sponge Kidney 41 0.040