Search results for KDM2B

80 hits were found for KDM2B

# Family MCID Name MIFTS Score
1
P MCR010 Microcephaly 60 16.658
2
P SYN057 Syndromic Intellectual Disability 38 13.488
3
WST001 West Syndrome 59 9.932
4
CHN016 Cohen Syndrome 60 9.932
5
EXN003 Exencephaly 30 8.948
6
DRV001 Dravet Syndrome 69 8.219
7
c MCR261 Microphthalmia, Syndromic 2 50 8.219
8
c MCR263 Microphthalmia, Syndromic 1 48 8.219
9
WVR001 Weaver Syndrome 56 8.219
10
P OVR042 Ovarian Cancer 88 4.643
11
P PRS040 Prostate Cancer 95 3.715
12
P GST053 Gastric Cancer 83 3.485
13
GLL048 Glial Tumor 52 3.395
14
GLM045 Glioma 63 3.395
15
GLB002 Glioblastoma 67 3.206
16
PNC041 Pancreatic Ductal Adenocarcinoma 51 3.105
17
OST159 Osteogenic Sarcoma 66 3.093
18
P PNC035 Pancreatic Cancer 86 3.089
19
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 2.998
20
BRK010 Burkitt Lymphoma 66 2.623
21
MYL009 Myelodysplastic Syndrome 67 2.584
22
c LKM061 Leukemia, Acute Myeloid 83 2.584
23
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 2.464
24
P LKM062 Leukemia, Acute Lymphoblastic 69 2.464
25
P MYL006 Myeloid Leukemia 61 2.464
26
P LKM002 Leukemia 67 2.464
27
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 2.464
28
SRC027 Sarcoma, Synovial 58 2.343
29
SPN035 Spindle Cell Sarcoma 54 2.343
30
SRC014 Sarcoma 65 2.343
31
CRV035 Cervical Cancer 73 2.335
32
P SPP010 Suppressor of Tumorigenicity 3 51 2.335
33
P BLD134 Bladder Cancer 79 2.195
34
P SCH015 Schizophrenia 74 2.195
35
MRF001 Marfan Syndrome 76 2.195
36
P NRB001 Neuroblastoma 66 2.041
37
INT389 Intellectual Developmental Disorder with Seizures and Language Delay 20 2.041
38
P BRS044 Breast Adenocarcinoma 58 1.865
39
KPS004 Kaposi Sarcoma 77 1.466
40
NRL016 Neural Tube Defects 81 1.385
41
HYP266 Hypoxia 57 1.136
42
P LYM118 Lymphoma 67 0.927
43
MLD018 Mild Cognitive Impairment 48 0.927
44
PLX002 Plexiform Neurofibroma 43 0.927
45
OST012 Osteoarthritis 77 0.927
46
P NRF002 Neurofibromatosis 57 0.927
47
NRF007 Neurofibroma 64 0.927
48
P BRS047 Breast Cancer 98 0.923
49
CLB010 Coloboma of Macula 53 0.729
50
RTN123 Retinochoroidal Coloboma 18 0.729
51
P ATS364 Autism 69 0.656
52
LYM133 Lymphoma, Hodgkin, Classic 74 0.656
53
AGN016 Aging 54 0.656
54
HRD029 Hereditary Leiomyomatosis and Renal Cell Cancer 56 0.656
55
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 0.656
56
DFF005 Diffuse Large B-Cell Lymphoma 54 0.656
57
NRD105 Neurodevelopmental Disorder with Seizures, Hypotonia, and Brain Imaging Abnormalities 22 0.656
58
GLC106 Glucocorticoid Resistance, Generalized 48 0.656
59
ACT119 Acute Promyelocytic Leukemia 62 0.656
60
DWN001 Down Syndrome 70 0.656
61
P RTN024 Retinoblastoma 73 0.656
62
P MDL005 Medulloblastoma 75 0.656
63
c BRD014 Bardet-Biedl Syndrome 2 53 0.656
64
PRM329 Premature Aging 36 0.656
65
BNS007 Bone Sarcoma 51 0.656
66
P CHR285 Chronic Myelomonocytic Leukemia 60 0.656
67
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.656
68
P BCL017 B-Cell Lymphoma 59 0.656
69
P EPL164 Epilepsy 68 0.656
70
ADN018 Adenoma 59 0.656
71
P LNG064 Lung Cancer Susceptibility 3 70 0.656
72
MST005 Mastitis 53 0.656
73
MCR013 Microphthalmia 60 0.656
74
THY020 Thyroid Hyalinizing Trabecular Adenoma 20 0.656
75
LMY003 Leiomyomatosis 44 0.656
76
INT020 Intravenous Leiomyomatosis 36 0.656
77
IRN002 Iron Metabolism Disease 57 0.656
78
CHR178 Chromosomal Triplication 34 0.656
79
MSL001 Measles 61 0.656
80
P LNG032 Lung Cancer 98 0.533
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