Search results for "[genes] CALM1"

33 hits were found for '[genes] CALM1'

# Family MCID Name MIFTS Score
1
c LNG098 Long Qt Syndrome 14 44 19.458
2
PRT037 Pertussis 64 16.445
3
P LNG028 Long Qt Syndrome 64 16.445
4
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 60 16.445
5
c VNT029 Ventricular Tachycardia, Catecholaminergic Polymorphic, 4 41 16.445
6
P ALZ034 Alzheimer Disease 92 14.709
7
CRD119 Cardiac Arrest 61 14.709
8
P SCL018 Scoliosis 55 14.709
9
IDP070 Idiopathic Scoliosis 41 14.709
10
P OTT001 Otitis Externa 47 12.738
11
SPR010 Sporotrichosis 47 12.738
12
HML015 Hemolytic Anemia Due to Triosephosphate Isomerase Deficiency 46 12.738
13
c LNG096 Long Qt Syndrome 15 44 12.738
14
GST052 Gestational Choriocarcinoma 42 12.738
15
OTM001 Otomycosis 38 12.738
16
P CLR001 Clear Cell Acanthoma 37 12.738
17
SPN033 Spontaneous Ocular Nystagmus 37 12.738
18
PRM026 Primary Systemic Mycosis 37 12.738
19
EXT056 External Ear Disease 36 12.738
20
c ACT037 Acute Dacryocystitis 33 12.738
21
ADL086 Adolescent Idiopathic Scoliosis 30 12.738
22
PRL005 Proliferative Fasciitis 30 12.738
23
c CLM002 Calm1-Related Catecholaminergic Polymorphic Ventricular Tachycardia 11 12.738
24
c LNG044 Long Qt Syndrome 1 62 10.401
25
c CRD093 Cardiomyopathy, Dilated, 1a 55 10.401
26
P PRM001 Primary Cutaneous Amyloidosis 50 10.401
27
c VNT013 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 49 10.401
28
c LBR012 Leber Congenital Amaurosis 2 47 10.401
29
SYN036 Syncope 47 10.401
30
c CRD104 Cardiomyopathy, Dilated, 1p 41 10.401
31
c VNT010 Ventricular Tachycardia, Catecholaminergic Polymorphic, 2 37 10.401
32
c DFN190 Deafness, Autosomal Dominant 2a 37 10.401
33
c DFN174 Deafness, Autosomal Recessive 44 36 10.401