Search results for PHOSPHATIDYLSERINE

110 hits were found for PHOSPHATIDYLSERINE

# Family MCID Name MIFTS Score
1
END072 Endotheliitis 46 0.168
2
P ANT006 Antiphospholipid Syndrome 59 0.152
3
P LKM002 Leukemia 75 0.113
4
SCK005 Sickle Cell Disease 54 0.113
5
SCT005 Scott Syndrome 48 0.113
6
NRN002 Neuronitis 43 0.113
7
c SYS001 Systemic Lupus Erythematosus 86 0.101
8
P LPS004 Lupus Erythematosus 69 0.101
9
P NRV007 Nervous System Disease 75 0.087
10
LSH001 Leishmaniasis 71 0.087
11
c HMP029 Hemophilia a 69 0.087
12
P ATT013 Attention Deficit-Hyperactivity Disorder 67 0.087
13
P HMP007 Hemophilia 61 0.087
14
P NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 57 0.087
15
URM002 Uremia 52 0.087
16
P DYS021 Dysautonomia 47 0.087
17
P KLZ004 Kala-Azar 1 31 0.087
18
STR067 Stroke, Ischemic 84 0.071
19
PLY001 Polycythemia Vera 75 0.071
20
P HPT021 Hepatitis 75 0.071
21
P LYM118 Lymphoma 71 0.071
22
DMN002 Dementia 68 0.071
23
P THL005 Thalassemia 65 0.071
24
P NRP001 Neuropathy 63 0.071
25
PRP030 Purpura 61 0.071
26
THR024 Thrombosis 61 0.071
27
P GLM045 Glioma 61 0.071
28
NRM005 Neuromuscular Disease 60 0.071
29
P PLY018 Polycythemia 60 0.071
30
P PLY019 Polyneuropathy 58 0.071
31
P DNG005 Dengue Virus 56 0.071
32
NRT004 Neuritis 55 0.071
33
PRP019 Peripheral Nervous System Disease 53 0.071
34
P PLY017 Polyarteritis Nodosa 51 0.071
35
ATN002 Autonomic Nervous System Disease 51 0.071
36
ATN005 Autonomic Dysfunction 51 0.071
37
ATN004 Autonomic Neuropathy 46 0.071
38
CRB009 Cerebritis 41 0.071
39
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 40 0.071
40
PLY112 Polyarteritis Nodosa, Childhood-Onset 39 0.071
41
END014 Endemic Typhus 38 0.071
42
c BLD140 Blood Group, I System 37 0.071
43
LNZ003 Lenz-Majewski Hyperostotic Dwarfism 35 0.071
44
MNT310 Mental Retardation, X-Linked, Syndromic, Snyder-Robinson Type 32 0.071
45
P RNG031 Ring Chromosome Y Syndrome 29 0.071
46
P CLR023 Colorectal Cancer 98 0.051
47
MYL069 Myeloma, Multiple 86 0.051
48
MLR004 Malaria 86 0.051
49
CYS001 Cystic Fibrosis 85 0.051
50
ULC004 Ulcerative Colitis 80 0.051
51
P HRT032 Heart Disease 80 0.051
52
c LKM071 Leukemia, Chronic Lymphocytic 75 0.051
53
c HPT073 Hepatitis C Virus 73 0.051
54
ISC006 Ischemic Heart Disease 73 0.051
55
c HPT001 Hepatitis C 73 0.051
56
LVR012 Liver Cirrhosis 73 0.051
57
PSY004 Psychotic Disorder 72 0.051
58
ANX010 Anxiety 72 0.051
59
MLN008 Melanoma 72 0.051
60
P ADN016 Adenocarcinoma 71 0.051
61
P ESS003 Essential Thrombocythemia 71 0.051
62
c BTT014 Beta-Thalassemia 70 0.051
63
P EPL164 Epilepsy 70 0.051
64
c HPT016 Hepatitis B 68 0.051
65
SRC014 Sarcoma 68 0.051
66
P LYM026 Lymphoblastic Leukemia 66 0.051
67
c LCL006 Localized Scleroderma 66 0.051
68
GLN010 Glanzmann Thrombasthenia 66 0.051
69
CTN007 Cutaneous Leishmaniasis 66 0.051
70
c CNT035 Central Nervous System Disease 65 0.051
71
c PRC016 Pre-Eclampsia 65 0.051
72
AGN016 Aging 65 0.051
73
P PNC044 Pancreatitis 64 0.051
74
ACT119 Acute Promyelocytic Leukemia 64 0.051
75
CLT003 Colitis 63 0.051
76
c THR092 Thrombophilia Due to Thrombin Defect 61 0.051
77
P NPH012 Nephrotic Syndrome 60 0.051
78
P BRN019 Bernard-Soulier Syndrome 60 0.051
79
P MNC007 Monocytic Leukemia 59 0.051
80
VSC003 Visceral Leishmaniasis 59 0.051
81
PLS007 Plasmodium Falciparum Malaria 59 0.051
82
P ENC018 Encephalopathy 58 0.051
83
P ECL001 Eclampsia 57 0.051
84
BRN022 Bronchiectasis 55 0.051
85
PYD001 Pyoderma Gangrenosum 55 0.051
86
P SZR006 Seizure Disorder 55 0.051
87
c OVR114 Ovarian Cancer 1 54 0.051
88
P RTN022 Retinal Vein Occlusion 53 0.051
89
CLN015 Colon Adenocarcinoma 53 0.051
90
HLL004 Hellp Syndrome 53 0.051
91
RTN023 Retinitis 52 0.051
92
NPH091 Nephrolithiasis, Calcium Oxalate 51 0.051
93
PYD002 Pyoderma 51 0.051
94
VCC001 Vaccinia 50 0.051
95
FCT001 Factor Viii Deficiency 50 0.051
96
c CNT016 Central Retinal Vein Occlusion 50 0.051
97
SHR069 Short-Rib Thoracic Dysplasia 6 with or Without Polydactyly 49 0.051
98
DWR001 Dwarfism 48 0.051
99
MCC002 Mucocutaneous Leishmaniasis 48 0.051
100
THR035 Thrombasthenia 46 0.051
101
HST016 Histiocytic Sarcoma 45 0.051
102
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.051
103
c CTR122 Cataract 5, Multiple Types 38 0.051
104
c LKM004 Leukemia, B-Cell, Chronic 37 0.051
105
c MLT151 Multiple Mitochondrial Dysfunctions Syndrome 5 36 0.051
106
c LKM056 Leukemia, Chronic Lymphocytic 2 35 0.051
107
c EPS039 Episodic Pain Syndrome, Familial, 1 33 0.051
108
CTN019 Cutaneous Polyarteritis Nodosa 29 0.051
109
ARL004 Aural Atresia, Congenital 27 0.051
110
HST008 Histiocytic and Dendritic Cell Cancer 26 0.051
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