Search results for "[genes] THPO"

49 hits were found for '[genes] THPO'

# Family MCID Name MIFTS Score
1
P MYL005 Myelofibrosis 62 19.775
2
P LKM002 Leukemia 63 18.498
3
LVR012 Liver Cirrhosis 57 15.633
4
P THR014 Thrombocytopenia 54 15.633
5
c THR090 Thrombocythemia 1 36 15.633
6
P APL001 Aplastic Anemia 68 13.983
7
P PLY018 Polycythemia 51 13.983
8
P PRT013 Portal Hypertension 49 13.983
9
DFC004 Deficiency Anemia 48 13.983
10
THR004 Thrombocytosis 48 13.983
11
PRP030 Purpura 47 13.983
12
IRN001 Iron Deficiency Anemia 45 13.983
13
MYL009 Myelodysplastic Syndrome 65 12.109
14
P ESS003 Essential Thrombocythemia 65 12.109
15
PLY125 Polycythemia Vera, Somatic 60 12.109
16
BRN082 Bernard-Soulier Syndrome, Type C 51 12.109
17
MGK001 Megakaryocytic Leukemia 48 12.109
18
BNM001 Bone Marrow Cancer 46 12.109
19
THR100 Thrombocytopenic Purpura, Autoimmune 45 12.109
20
HYP299 Hyperostosis, Endosteal 45 12.109
21
HMR001 Hemorrhagic Thrombocythemia 44 12.109
22
P PNC001 Pancytopenia 44 12.109
23
HYP063 Hypersplenism 41 12.109
24
PRN019 Perinatal Necrotizing Enterocolitis 41 12.109
25
c CHR092 Chronic Myeloproliferative Disease 40 12.109
26
BLD053 Blood Platelet Disease 35 12.109
27
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 31 12.109
28
c ACQ005 Acquired Thrombocytopenia 31 12.109
29
P DMN001 Diamond-Blackfan Anemia 65 9.887
30
HMT002 Hematologic Cancer 57 9.887
31
DNG003 Dengue Disease 57 9.887
32
THR009 Thrombocytopenia-Absent Radius Syndrome 52 9.887
33
P IDP064 Idiopathic Neutropenia 42 9.887
34
EXN001 Exanthema Subitum 42 9.887
35
HPT046 Hepatic Veno-Occlusive Disease 40 9.887
36
c THR103 Thrombocytopenia, Congenital Amegakaryocytic 40 9.887
37
THR042 Thrombocytopenia, X-Linked 40 9.887
38
P BLD051 Blood Coagulation Disease 37 9.887
39
SPL012 Splenic Disease 34 9.887
40
c PRM225 Primary Thrombocytopenia 32 9.887
41
FLC001 Folic Acid Deficiency Anemia 27 9.887
42
ATM012 Autoimmune Disease of Blood 27 9.887
43
SPL009 Splenic Sequestration 23 9.887
44
CYC007 Cyclic Thrombocytopenia 20 9.887
45
c LKM061 Leukemia, Acute Myeloid 66 6.991
46
P CRN015 Cornelia De Lange Syndrome 60 6.991
47
HRD137 Hereditary Isolated Aplastic Anemia 14 6.991
48
HRD118 Hereditary Thrombocytosis with Transverse Limb Defect 6 6.991
49
c THP002 Thpo-Related Essential Thrombocythemia 6 6.991