Search results for PHOSPHATIDYLSERINE

105 hits were found for PHOSPHATIDYLSERINE

# Family MCID Name MIFTS Score
1
END072 Endotheliitis 42 0.162
2
P ANT006 Antiphospholipid Syndrome 56 0.154
3
P LKM002 Leukemia 71 0.115
4
SCK005 Sickle Cell Disease 51 0.115
5
NRN002 Neuronitis 41 0.115
6
c SYS001 Systemic Lupus Erythematosus 86 0.103
7
P LPS004 Lupus Erythematosus 64 0.103
8
SCT005 Scott Syndrome 53 0.103
9
ATT013 Attention Deficit-Hyperactivity Disorder 69 0.089
10
LSH001 Leishmaniasis 66 0.089
11
c HMP029 Hemophilia a 63 0.089
12
P HMP007 Hemophilia 57 0.089
13
URM002 Uremia 48 0.089
14
P LYM118 Lymphoma 69 0.072
15
P HPT021 Hepatitis 69 0.072
16
DMN002 Dementia 65 0.072
17
P THL005 Thalassemia 64 0.072
18
P GLM045 Glioma 60 0.072
19
P PLY018 Polycythemia 58 0.072
20
PRP030 Purpura 58 0.072
21
THR024 Thrombosis 57 0.072
22
P PLY017 Polyarteritis Nodosa 51 0.072
23
P DYS021 Dysautonomia 44 0.072
24
CRB009 Cerebritis 39 0.072
25
NTR005 Nutritional Deficiency Disease 36 0.072
26
c STR092 Striatal Degeneration, Autosomal Dominant 2 27 0.072
27
HYP711 Hypotonia, Ataxia, and Delayed Development Syndrome 26 0.072
28
P CLR023 Colorectal Cancer 97 0.051
29
CYS001 Cystic Fibrosis 83 0.051
30
MLR004 Malaria 83 0.051
31
P MLT019 Multiple Myeloma 83 0.051
32
HV1006 Hiv-1 80 0.051
33
c CHR090 Chronic Lymphocytic Leukemia 76 0.051
34
ULC004 Ulcerative Colitis 76 0.051
35
P HRT032 Heart Disease 75 0.051
36
c HPT073 Hepatitis C Virus 73 0.051
37
P NRV007 Nervous System Disease 71 0.051
38
P ADN016 Adenocarcinoma 69 0.051
39
c HPT001 Hepatitis C 68 0.051
40
ISC006 Ischemic Heart Disease 68 0.051
41
LVR012 Liver Cirrhosis 67 0.051
42
P EPL164 Epilepsy 66 0.051
43
SRC014 Sarcoma 66 0.051
44
c HPT016 Hepatitis B 64 0.051
45
GLN010 Glanzmann Thrombasthenia 63 0.051
46
MLN008 Melanoma 62 0.051
47
CTN007 Cutaneous Leishmaniasis 62 0.051
48
P LYM026 Lymphoblastic Leukemia 62 0.051
49
P PNC044 Pancreatitis 61 0.051
50
c LCL006 Localized Scleroderma 61 0.051
51
CLT003 Colitis 60 0.051
52
c CNT035 Central Nervous System Disease 60 0.051
53
P ENC018 Encephalopathy 59 0.051
54
P NRP001 Neuropathy 59 0.051
55
P NPH012 Nephrotic Syndrome 59 0.051
56
c PRC016 Pre-Eclampsia 56 0.051
57
P SZR006 Seizure Disorder 56 0.051
58
NRM005 Neuromuscular Disease 56 0.051
59
P PLY019 Polyneuropathy 56 0.051
60
VSC003 Visceral Leishmaniasis 56 0.051
61
PRP019 Peripheral Nervous System Disease 55 0.051
62
P MNC007 Monocytic Leukemia 55 0.051
63
PLS007 Plasmodium Falciparum Malaria 55 0.051
64
P HYP620 Hypoprothrombinemia 54 0.051
65
CND002 Conduct Disorder 54 0.051
66
P ECL001 Eclampsia 54 0.051
67
SLP005 Sleep Disorder 53 0.051
68
PYD001 Pyoderma Gangrenosum 51 0.051
69
CLN015 Colon Adenocarcinoma 50 0.051
70
RTN023 Retinitis 50 0.051
71
BRN022 Bronchiectasis 50 0.051
72
HLL004 Hellp Syndrome 50 0.051
73
c DYS166 Dysautonomia, Familial 49 0.051
74
LRN003 Learning Disability 49 0.051
75
ATN005 Autonomic Dysfunction 49 0.051
76
PYD002 Pyoderma 48 0.051
77
ATN002 Autonomic Nervous System Disease 48 0.051
78
DWR001 Dwarfism 47 0.051
79
MCC002 Mucocutaneous Leishmaniasis 46 0.051
80
VCC001 Vaccinia 46 0.051
81
P HRD021 Hereditary Sensory Neuropathy 46 0.051
82
SNS003 Sensory Peripheral Neuropathy 45 0.051
83
ACR041 Acromelic Frontonasal Dysostosis 45 0.051
84
ATN004 Autonomic Neuropathy 45 0.051
85
PHY002 Physical Disorder 43 0.051
86
BRT030 Birth Defects 43 0.051
87
PRD011 Proud Syndrome 42 0.051
88
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 41 0.051
89
HST016 Histiocytic Sarcoma 40 0.051
90
c HRD088 Hereditary Neuropathies 40 0.051
91
THR035 Thrombasthenia 39 0.051
92
P RTN022 Retinal Vein Occlusion 38 0.051
93
BLD054 Blood Protein Disease 37 0.051
94
WTH001 Withdrawal Disorder 37 0.051
95
c CNG031 Congenital Nervous System Abnormality 37 0.051
96
c CNT016 Central Retinal Vein Occlusion 36 0.051
97
ALR002 Al-Raqad Syndrome 36 0.051
98
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 35 0.051
99
RDN001 Reading Disorder 34 0.051
100
END014 Endemic Typhus 31 0.051
101
LNZ003 Lenz-Majewski Hyperostotic Dwarfism 28 0.051
102
CTN019 Cutaneous Polyarteritis Nodosa 28 0.051
103
ATN001 Autonomic Peripheral Neuropathy 17 0.051
104
c DYS033 Dysautonomia Like Disorder 16 0.051
105
HRD059 Hereditary Peripheral Nervous Disorder 11 0.051
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