Search results for zbtb18

Showing 25 of 58 hits for zbtb18
# Family MCID Name MIFTS Score
1
c INT513 Intellectual Developmental Disorder, Autosomal Dominant 22 36 46.456
2
P MCR010 Microcephaly 59 14.476
3
c RTN114 Retinitis Pigmentosa 58 34 9.848
4
c CNG513 Congenital Ptosis 51 7.999
5
CHR582 Chromosome 3q29 Duplication Syndrome 33 7.999
6
c DVL078 Developmental and Epileptic Encephalopathy 54 36 7.999
7
c CNG031 Congenital Nervous System Abnormality 32 7.999
8
BRT005 Barth Syndrome 57 7.999
9
c DVL053 Developmental and Epileptic Encephalopathy 27 38 7.999
10
TRN017 Transient Neonatal Neutropenia 13 7.999
11
TRN013 Transient Neonatal Thrombocytopenia 18 7.999
12
GLB002 Glioblastoma 67 2.663
13
HYP265 Hypotonia 46 2.157
14
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 46 1.697
15
CRP032 Corpus Callosum, Agenesis of 55 1.324
16
P HPT023 Hepatocellular Carcinoma 96 1.257
17
CHR662 Chromosome 15q13.3 Deletion Syndrome 41 1.257
18
P SYN057 Syndromic Intellectual Disability 33 1.257
20
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 1.178
21
P BRS047 Breast Cancer 97 0.712
22
BRK010 Burkitt Lymphoma 67 0.503
23
P PNC035 Pancreatic Cancer 91 0.503
24
P GLM040 Glioma Susceptibility 1 71 0.503
25
P OVR042 Ovarian Cancer 89 0.503
1 2 3 Next
Content
Loading form....