Search results for camk2b

Showing 25 of 88 hits for camk2b
# Family MCID Name MIFTS Score
1
c INT562 Intellectual Developmental Disorder, Autosomal Dominant 54 27 39.762
2
c CNG031 Congenital Nervous System Abnormality 32 18.288
3
P NRV007 Nervous System Disease 67 18.288
4
P MCR010 Microcephaly 59 14.108
5
P ATS364 Autism 74 14.005
6
c ATS007 Autism Spectrum Disorder 70 14.005
7
P FRG001 Fragile X Syndrome 69 11.435
8
P DYS154 Dystonia 66 9.730
9
c ATS203 Autosomal Dominant Non-Syndromic Intellectual Disability 34 8.558
10
c ANT085 Anterior Segment Dysgenesis 5 47 8.086
11
P FCL005 Focal Segmental Glomerulosclerosis 59 8.086
12
c INT561 Intellectual Developmental Disorder, Autosomal Dominant 53 26 1.527
13
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 46 1.527
14
HYP265 Hypotonia 46 1.492
15
OTP003 Oto-Palatal-Digital Syndrome 36 1.382
16
HYP037 Hyperhomocysteinemia 51 1.284
17
RNL114 Renal Cell Carcinoma, Nonpapillary 80 1.161
18
RNL065 Renal Cell Carcinoma, Papillary, 1 79 1.161
19
CLL002 Collecting Duct Carcinoma 64 1.161
20
P NRB001 Neuroblastoma 62 1.123
21
P EPS003 Episodic Ataxia 60 1.080
22
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 66 1.028
23
P SCL018 Scoliosis 56 1.028
24
P EPL164 Epilepsy 71 1.028
25
MTR086 Motor Stereotypies 31 1.028
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