Search results for "[genes] THPO"

49 hits were found for '[genes] THPO'

# Family MCID Name MIFTS Score
1
P MYL005 Myelofibrosis 68 19.775
2
P LKM002 Leukemia 70 18.498
3
LVR012 Liver Cirrhosis 66 15.633
4
P THR014 Thrombocytopenia 62 15.633
5
c THR090 Thrombocythemia 1 42 15.633
6
P APL001 Aplastic Anemia 73 13.983
7
DFC004 Deficiency Anemia 62 13.983
8
P PRT013 Portal Hypertension 59 13.983
9
PRP030 Purpura 58 13.983
10
P PLY018 Polycythemia 57 13.983
11
THR004 Thrombocytosis 56 13.983
12
IRN001 Iron Deficiency Anemia 50 13.983
13
MYL009 Myelodysplastic Syndrome 72 12.109
14
P ESS003 Essential Thrombocythemia 66 12.109
15
PLY125 Polycythemia Vera, Somatic 64 12.109
16
BNM001 Bone Marrow Cancer 58 12.109
17
THR100 Thrombocytopenic Purpura, Autoimmune 55 12.109
18
MGK001 Megakaryocytic Leukemia 54 12.109
19
c CHR092 Chronic Myeloproliferative Disease 53 12.109
20
BRN082 Bernard-Soulier Syndrome, Type C 52 12.109
21
P PNC001 Pancytopenia 51 12.109
22
HMR001 Hemorrhagic Thrombocythemia 50 12.109
23
HYP299 Hyperostosis, Endosteal 49 12.109
24
BLD053 Blood Platelet Disease 47 12.109
25
PRN019 Perinatal Necrotizing Enterocolitis 46 12.109
26
HYP063 Hypersplenism 46 12.109
27
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 42 12.109
28
c ACQ005 Acquired Thrombocytopenia 42 12.109
29
P DMN001 Diamond-Blackfan Anemia 71 9.887
30
HMT002 Hematologic Cancer 63 9.887
31
DNG003 Dengue Disease 63 9.887
32
THR009 Thrombocytopenia-Absent Radius Syndrome 52 9.887
33
P IDP064 Idiopathic Neutropenia 51 9.887
34
HPT046 Hepatic Veno-Occlusive Disease 48 9.887
35
P BLD051 Blood Coagulation Disease 46 9.887
36
THR042 Thrombocytopenia, X-Linked 45 9.887
37
c THR103 Thrombocytopenia, Congenital Amegakaryocytic 45 9.887
38
c PRM225 Primary Thrombocytopenia 44 9.887
39
EXN001 Exanthema Subitum 44 9.887
40
SPL012 Splenic Disease 43 9.887
41
FLC001 Folic Acid Deficiency Anemia 39 9.887
42
ATM012 Autoimmune Disease of Blood 38 9.887
43
CYC007 Cyclic Thrombocytopenia 27 9.887
44
SPL009 Splenic Sequestration 27 9.887
45
c LKM061 Leukemia, Acute Myeloid 71 6.991
46
P CRN015 Cornelia De Lange Syndrome 65 6.991
47
HRD137 Hereditary Isolated Aplastic Anemia 17 6.991
48
c THP002 Thpo-Related Essential Thrombocythemia 8 6.991
49
HRD118 Hereditary Thrombocytosis with Transverse Limb Defect 7 6.991