Search results for IVL

87 hits were found for IVL

# Family MCID Name MIFTS Score
1
CHL122 Cholesteatoma of Middle Ear 50 3.044
2
SKN016 Skin Disease 63 2.670
3
c BSL007 Basal Cell Carcinoma 68 2.636
4
P SKN015 Skin Carcinoma 66 2.636
5
P PSR002 Psoriasis 62 2.636
6
BLL006 Bullous Pemphigoid 62 2.636
7
DRM006 Dermatitis 61 2.636
8
SQM006 Squamous Cell Carcinoma 60 2.636
9
P EPD003 Epidermolysis Bullosa Simplex 58 2.636
10
EPD002 Epidermolytic Hyperkeratosis 56 2.636
11
ICH001 Ichthyosis Vulgaris 55 2.636
12
P PRK001 Porokeratosis 55 2.636
13
PPL022 Papilloma 54 2.636
14
P LCH002 Lichen Planus 53 2.636
15
MCP006 Mucoepidermoid Carcinoma 50 2.636
16
MLL001 Molluscum Contagiosum 50 2.636
17
FBR054 Fibroma 44 2.636
18
P DRM053 Dermatitis, Atopic 66 2.192
19
SVR004 Severe Combined Immunodeficiency 73 2.153
20
P ESP024 Esophagitis 62 2.153
21
DRR014 Darier-White Disease 60 2.153
22
c BNG091 Benign Chronic Pemphigus 58 2.153
23
CNT047 Contact Dermatitis 58 2.153
24
PMP006 Pemphigus Vulgaris, Familial 57 2.153
25
P ICH004 Ichthyosis 54 2.153
26
RCS002 Recessive Dystrophic Epidermolysis Bullosa 54 2.153
27
P EPD016 Epidermolysis Bullosa 53 2.153
28
KRT009 Keratosis 51 2.153
29
MNL001 Monilethrix 48 2.153
30
P KRT005 Keratoacanthoma 48 2.153
31
ADN009 Adenosquamous Carcinoma 47 2.153
32
DSC009 Discoid Lupus Erythematosus 42 2.153
33
CRV045 Cervical Intraepithelial Neoplasia 39 2.153
34
BWN006 Bowen's Disease 32 2.153
35
NVS017 Nevus, Epidermal 68 1.522
36
c ATS013 Autosomal Recessive Congenital Ichthyosis 63 1.522
37
KRT071 Keratosis, Seborrheic 58 1.522
38
SKN022 Skin Squamous Cell Carcinoma 57 1.522
39
c ICH069 Ichthyosis, Congenital, Autosomal Recessive 4b 51 1.522
40
IRR003 Irritant Dermatitis 49 1.522
41
DYS009 Dysthymic Disorder 49 1.522
42
DNT045 Dental Anomalies and Short Stature 49 1.522
43
SCL003 Social Phobia 48 1.522
44
HYP016 Hypochondriasis 47 1.522
45
AGR002 Agoraphobia 45 1.522
46
PHB001 Phobic Disorder 41 1.522
47
PHB003 Phobia, Specific 41 1.522
48
EPD070 Epidermoid Cysts 37 1.522
49
P CLR001 Clear Cell Acanthoma 34 1.522
50
ELS002 Elastosis Perforans Serpiginosa 30 1.522
51
INT379 Integumentary System Disease 28 1.522
52
ERY014 Erythrokeratoderma 27 1.522
53
EPD004 Epidermolytic Acanthoma 26 1.522
54
BRS013 Borst-Jadassohn Intraepidermal Carcinoma 25 1.522
55
P STM003 Stomach Carcinoma in Situ 25 1.522
56
CRT007 Cortical Deafness 24 1.522
57
EPD010 Epidermal Appendage Tumor 17 1.522
58
PRD001 Predominantly Cortical Thymoma 17 1.522
59
INT020 Intravenous Leiomyomatosis 36 0.139
60
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.088
61
P MYC007 Myocardial Infarction 70 0.088
62
P CRN300 Coronary Heart Disease 1 63 0.088
63
LPP008 Lipoprotein Quantitative Trait Locus 62 0.088
64
ISC004 Ischemia 58 0.088
65
P BCL017 B-Cell Lymphoma 58 0.088
66
ART140 Arteries, Anomalies of 52 0.088
67
INT221 Intravascular Large B-Cell Lymphoma 35 0.088
68
P CRN133 Coronary Artery Disease, Autosomal Dominant, 1 32 0.088
69
P CLR023 Colorectal Cancer 99 0.062
70
P LYM118 Lymphoma 68 0.062
71
P NTR004 Neutropenia 63 0.062
72
P ENC004 Encephalitis 61 0.062
73
CRV038 Cervical Squamous Cell Carcinoma 58 0.062
74
P PLY019 Polyneuropathy 56 0.062
75
NRG002 Neurogenic Bladder 55 0.062
76
MYM001 Myoma 54 0.062
77
P CNT005 Central Nervous System Lymphoma 53 0.062
78
LMY002 Leiomyoma 52 0.062
79
PNG002 Pain Agnosia 51 0.062
80
OCL069 Ocular Motor Apraxia 51 0.062
81
VCC001 Vaccinia 49 0.062
82
c PRM226 Primary Central Nervous System Lymphoma 48 0.062
83
CYT002 Cytokine Deficiency 42 0.062
84
PRS063 Paresthesia 41 0.062
85
TST004 Testicular Lymphoma 39 0.062
86
c ATM075 Autoimmune Encephalitis 38 0.062
87
c CHR020 Chronic Interstitial Cystitis 37 0.062
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