Search results for kirrel3

Showing 25 of 57 hits for kirrel3
# Family MCID Name MIFTS Score
1
P ATS364 Autism 74 14.647
2
P FCL005 Focal Segmental Glomerulosclerosis 59 12.074
3
JCB001 Jacobsen Syndrome 48 11.036
4
c INT515 Intellectual Developmental Disorder, Autosomal Dominant 4 26 10.722
5
c ATS203 Autosomal Dominant Non-Syndromic Intellectual Disability 34 9.475
6
HML046 Heimler Syndrome 2 33 8.538
7
c FML015 Familial Nephrotic Syndrome 47 8.538
8
c ATS007 Autism Spectrum Disorder 70 5.621
9
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 46 3.802
10
ESP021 Esophageal Cancer 83 1.424
11
ESP027 Esophagus Squamous Cell Carcinoma 58 1.424
12
DND001 Dandy-Walker Syndrome 50 1.303
13
P ATT013 Attention Deficit-Hyperactivity Disorder 66 1.303
14
P CRB045 Cerebellar Hypoplasia 40 1.303
15
P MCR010 Microcephaly 59 1.268
16
c INT514 Intellectual Developmental Disorder, Autosomal Dominant 3 32 1.187
17
P BRS047 Breast Cancer 97 0.712
18
P GLM040 Glioma Susceptibility 1 71 0.630
19
NRF008 Neurofibromatosis-Noonan Syndrome 79 0.630
20
c MSM022 Mismatch Repair Cancer Syndrome 1 73 0.630
21
MNN043 Meningioma, Familial 81 0.630
22
c GLM025 Glioma Susceptibility 2 32 0.630
23
c GLM047 Glioma Susceptibility 3 34 0.630
24
c GLM043 Glioma Susceptibility 9 31 0.630
25
P OLG002 Oligodendroglioma 66 0.630
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