Search results for "trichoepithelioma"

The MalaCard for "trichoepithelioma" has been retired.
Searching MalaCards for entries containing "trichoepithelioma"

69 hits were found for 'trichoepithelioma'

# Family MCID Name MIFTS Score
1
P MLT048 Multiple Familial Trichoepithelioma 28 7.633
2
c TRC095 Trichoepithelioma, Multiple Familial, 1 18 6.587
3
c TRC094 Trichoepithelioma, Multiple Familial, 2 12 5.533
4
VLV022 Vulvar Trichoepithelioma 3 3.512
5
RMB001 Rombo Syndrome 16 2.523
6
c BSL007 Basal Cell Carcinoma 65 0.364
7
BRK001 Brooke-Spiegler Syndrome 48 0.275
8
CYL004 Cylindromatosis, Familial 29 0.151
9
P SPR013 Spiradenoma 36 0.137
10
INF027 Infiltrative Basal Cell Carcinoma 28 0.123
11
SQM006 Squamous Cell Carcinoma 70 0.087
12
P FNC043 Fanconi Anemia, Complementation Group E 55 0.087
13
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.087
14
P SKN013 Skin Benign Neoplasm 43 0.087
15
c BSL024 Basal Cell Carcinoma 1 42 0.087
16
ADN002 Adenoiditis 39 0.087
17
P SYR003 Syringoma 37 0.087
18
ALR002 Al-Raqad Syndrome 36 0.087
19
STR067 Stroke, Ischemic 75 0.061
20
P ADN016 Adenocarcinoma 69 0.061
21
CRB037 Cerebral Palsy 66 0.061
22
PLM033 Pulmonary Embolism 60 0.061
23
P THR015 Thrombophilia 59 0.061
24
THR024 Thrombosis 57 0.061
25
HYP266 Hypoxia 56 0.061
26
P BDD001 Budd-Chiari Syndrome 56 0.061
27
P ANT006 Antiphospholipid Syndrome 56 0.061
28
PTN001 Patent Foramen Ovale 55 0.061
29
c THR092 Thrombophilia Due to Thrombin Defect 54 0.061
30
c THR082 Thrombophilia Due to Activated Protein C Resistance 54 0.061
31
P ECL001 Eclampsia 54 0.061
32
PRT014 Protein S Deficiency 53 0.061
33
THR016 Thrombophlebitis 53 0.061
34
P SCH018 Schizencephaly 52 0.061
35
PRT011 Protein C Deficiency 52 0.061
36
KRT009 Keratosis 52 0.061
37
P PRC031 Preeclampsia/eclampsia 1 51 0.061
38
P HMC002 Homocystinuria 50 0.061
39
INT075 Intracranial Hypertension 50 0.061
40
HPT074 Hepatic Adenoma, Somatic 50 0.061
41
HLL004 Hellp Syndrome 50 0.061
42
HYP037 Hyperhomocysteinemia 50 0.061
43
THR104 Thrombophilia Due to Antithrombin Iii Deficiency 49 0.061
44
PRT018 Portal Vein Thrombosis 49 0.061
45
P PRN026 Porencephaly 48 0.061
46
VND001 Vein Disease 47 0.061
47
PLC007 Placental Abruption 47 0.061
48
P HYP087 Hypotrichosis 46 0.061
49
FBR054 Fibroma 46 0.061
50
P RTN014 Retinal Artery Occlusion 44 0.061
51
HMC020 Homocystinuria, B6-Responsive and Nonresponsive Types 43 0.061
52
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.061
53
c CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 41 0.061
54
APC004 Apocrine Adenocarcinoma 39 0.061
55
AMR003 Amaurosis Fugax 38 0.061
56
INT078 Intracranial Thrombosis 36 0.061
57
HMC014 Homocysteinemia 35 0.061
58
ADP007 Adie Pupil 34 0.061
59
SPN185 Spinal Cord Infarction 34 0.061
60
LVD002 Livedoid Vasculopathy 32 0.061
61
NDL009 Nodular Basal Cell Carcinoma 31 0.061
62
ART110 Arteritic Anterior Ischemic Optic Neuropathy 31 0.061
63
PRG092 Pregnancy Loss, Recurrent 1 31 0.061
64
INF133 Inferior Vena Cava Interruption 29 0.061
65
MRP002 Morpheaform Basal Cell Carcinoma 27 0.061
66
HNM002 Hinman Syndrome 25 0.061
67
MTH044 Mthfr Gene Mutation 21 0.061
68
AND005 Androgen Insensitivity Syndrome, Mild 16 0.061
69
TRC052 Trichofolliculoma 14 0.061