Search results for "[genes] F13A1"

42 hits were found for '[genes] F13A1'

# Family MCID Name MIFTS Score
1
FCT005 Factor Xiii Deficiency 39 18.885
2
FCT011 Factor Xiiia Deficiency 23 17.485
3
P MYC007 Myocardial Infarction 76 15.961
4
LNG024 Langerhans-Cell Histiocytosis 63 14.276
5
PLM033 Pulmonary Embolism 53 14.276
6
CRB039 Cerebrovascular Disease 58 12.363
7
DRM014 Dermatofibrosarcoma Protuberans 54 12.363
8
P HMN013 Hemangiopericytoma 46 12.363
9
NRF007 Neurofibroma 45 12.363
10
PRP007 Priapism 41 12.363
11
c JVN003 Juvenile Xanthogranuloma 40 12.363
12
FBR003 Fibrous Histiocytoma 37 12.363
13
FBR054 Fibroma 36 12.363
14
GRN007 Granuloma Annulare 35 12.363
15
CTN004 Cutaneous Fibrous Histiocytoma 33 12.363
16
KPS004 Kaposi Sarcoma 65 10.095
17
VND002 Van Der Woude Syndrome 54 10.095
18
c THR092 Thrombophilia Due to Thrombin Defect 49 10.095
19
PTN001 Patent Foramen Ovale 48 10.095
20
c JVN016 Juvenile Hyaline Fibromatosis 47 10.095
21
P DYS026 Dysfibrinogenemia 45 10.095
22
MLT016 Multicentric Reticulohistiocytosis 43 10.095
23
NPH018 Nephrogenic Systemic Fibrosis 43 10.095
24
HNC001 Henoch-Schoenlein Purpura 41 10.095
25
HYP074 Hypersensitivity Vasculitis 38 10.095
26
ANG017 Angiolipoma 36 10.095
27
ERY017 Erythema Elevatum Diutinum 35 10.095
28
XNT009 Xanthoma Disseminatum 34 10.095
29
NNL001 Non-Langerhans-Cell Histiocytosis 32 10.095
30
SCL025 Scleromyxedema 31 10.095
31
MLG065 Malignant Fibroxanthoma 29 10.095
32
MYF001 Myofibroma 28 10.095
33
c HYP072 Hypersensitivity Reaction Type Iii Disease 25 10.095
34
FBR001 Fibrous Meningioma 24 10.095
35
c PRT045 Prothrombin-Related Thrombophilia 23 10.095
36
P PPL026 Papular Mucinosis 22 10.095
37
CRP004 Corpus Luteum Cyst 21 10.095
38
PRG077 Progressive Nodular Histiocytosis 21 10.095
39
GNR023 Generalized Eruptive Histiocytosis 20 10.095
40
SLF008 Self-Healing Papular Mucinosis 12 10.095
41
ALK005 Alk+ Histiocytosis 10 10.095
42
c MSC124 Muscular Dystrophy, Congenital 50 7.138