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"

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

# Family MCID Name MIFTS Score
1
P LNG032 Lung Cancer 94 0.397
2
PRS047 Prostatitis 56 0.389
3
P PNC044 Pancreatitis 60 0.384
4
NRN002 Neuronitis 42 0.359
5
P ADN016 Adenocarcinoma 69 0.345
6
P PRS040 Prostate Cancer 89 0.336
7
P CLR023 Colorectal Cancer 97 0.316
8
P OVR042 Ovarian Cancer 75 0.287
9
P NRB001 Neuroblastoma 69 0.246
10
GST053 Gastric Cancer 77 0.244
11
P LYM026 Lymphoblastic Leukemia 60 0.216
12
ADN018 Adenoma 59 0.201
13
HYP056 Hypoglycemia 61 0.165
14
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.161
15
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 0.158
16
P ATR011 Atrial Fibrillation 64 0.157
17
P CTR002 Cataract 57 0.156
18
ISC006 Ischemic Heart Disease 68 0.153
19
CLT003 Colitis 59 0.147
20
P UTR038 Uterine Disease 40 0.146
21
PRM097 Primary Immunodeficiency Disease 61 0.141
22
P HYP086 Hypothyroidism 65 0.136
23
TTH006 Tooth Disease 52 0.135
24
LPD008 Lipid Metabolism Disorder 58 0.124
25
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.123
26
P END044 Endometriosis 53 0.121
27
RNL101 Renal Cell Carcinoma, Papillary 67 0.119
28
P CNJ013 Conjunctivitis 65 0.117
29
PPL022 Papilloma 55 0.114
30
MDS022 Mediastinitis 41 0.113
31
HYD012 Hydrops Fetalis 44 0.113
32
P CLC005 Celiac Disease 67 0.111
33
BRN106 Burns 52 0.110
34
FML037 Female Breast Cancer 51 0.109
35
EPD016 Epidermolysis Bullosa 57 0.109
36
GTR002 Goiter 54 0.103
37
SPN051 Spondylitis 50 0.099
38
CHR005 Chorioamnionitis 48 0.097
39
LMB062 Limb Ischemia 48 0.097
40
P PLY011 Polycystic Ovary Syndrome 66 0.096
41
P HMR012 Hemorrhagic Fever 55 0.095
42
ATM014 Autoimmune Disease of Endocrine System 37 0.093
43
ALC007 Alcohol Dependence 65 0.090
44
GLC003 Glucose Intolerance 55 0.087
45
GRW007 Growth Hormone Deficiency 48 0.080
46
P ESS003 Essential Thrombocythemia 68 0.080
47
CRN030 Coronary Stenosis 50 0.077
48
THY030 Thyroid Gland Disease 51 0.077
49
TXC005 Toxic Shock Syndrome 61 0.075
50
ORL014 Oral Pharyngeal Disorders 14 0.071
51
P FML035 Familial Hyperlipidemia 50 0.069
52
P LCT001 Lactic Acidosis 52 0.065
53
GLC006 Galactosemia 67 0.065
54
HLL004 Hellp Syndrome 49 0.065
55
ADN001 Adenosine Deaminase Deficiency 45 0.063
56
P SDD001 Sudden Infant Death Syndrome 61 0.062
57
PRT082 Preterm Premature Rupture of the Membranes 47 0.059
58
P STR020 Strabismus 53 0.059
59
GGN002 Gigantism 27 0.059
60
TWN001 Twin-to-Twin Transfusion Syndrome 46 0.056
61
SHW002 Shwachman-Diamond Syndrome 60 0.053
62
P EPD002 Epidermolytic Hyperkeratosis 49 0.046
63
FNT004 Fainting 33 0.045
64
AMN006 Aminoaciduria 42 0.044
65
MDL009 Medullary Sponge Kidney 40 0.039