|
OMIM |
Link |
Information
gain |
01 |
|
|
DWS
|
[NCBI]
|
0.0285762
|
|
|
|
dandy-walker-like malformation with atrioventricular septal defect
|
[NCBI]
|
0.00416157
|
|
|
|
dandy-walker malformation with mental retardation, basal ganglia disease, and seizures
|
[NCBI]
|
0.00197857
|
|
|
|
JBTS1
|
[NCBI]
|
0.00188674
|
|
|
|
renal-hepatic-pancreatic dysplasia with dandy-walker cyst
|
[NCBI]
|
0.00111801
|
|
|
|
varadi-papp syndrome
|
[NCBI]
|
0.000640161
|
|
|
|
marden-walker syndrome
|
[NCBI]
|
0.000582381
|
|
|
|
OFD3
|
[NCBI]
|
0.000476705
|
|
|
|
aase-smith syndrome i
|
[NCBI]
|
0.000476705
|
|
|
|
coffin-siris syndrome
|
[NCBI]
|
0.000458757
|
|
|
|
FRNS
|
[NCBI]
|
0.000427768
|
|
|
|
MKS1
|
[NCBI]
|
0.000379458
|
|
|
|
OFD9
|
[NCBI]
|
0.000355303
|
|
|
|
cleidocranial dysplasia with micrognathia, absent thumbs, and distal aphalangia
|
[NCBI]
|
0.00030871
|
|
|
|
DA5
|
[NCBI]
|
0.000273772
|
|
|
|
MVA
|
[NCBI]
|
0.000261675
|
|
|
|
dandy-walker malformation with postaxial polydactyly
|
[NCBI]
|
0.000261456
|
|
|
|
mohr syndrome
|
[NCBI]
|
0.000223033
|
|
|
|
phace association
|
[NCBI]
|
0.000188559
|
|
|
|
MEB
|
[NCBI]
|
0.000134618
|
|
|
|
walker-warburg syndrome
|
[NCBI]
|
0.000132105
|
|
|
|
dandy-walker malformation with mental retardation, macrocephaly, myopia, and brachytelephalangy
|
[NCBI]
|
0.000130439
|
|
|
|
craniosynostosis, sagittal, with dandy-walker malformation and hydrocephalus
|
[NCBI]
|
0.000130439
|
|
|
|
PCD
|
[NCBI]
|
0.000122588
|
|
|
|
FCMD
|
[NCBI]
|
0.000121273
|
|
|
|
sebaceous nevus syndrome and hemimegalencephaly
|
[NCBI]
|
0.000107971
|
|
|
|
CDG2D
|
[NCBI]
|
0.000107971
|
|
|
|
ZIC4
|
[NCBI]
|
0.00010573
|
|
|
|
ZIC1
|
[NCBI]
|
9.19492e-05
|
|
|
|
hemangiomas, cavernous, of face and supraumbilical midline raphe
|
[NCBI]
|
8.98999e-05
|
|
|
|
PCS
|
[NCBI]
|
7.77866e-05
|
|
|
|
oculocerebrocutaneous syndrome
|
[NCBI]
|
7.46973e-05
|
|
|
|
hydrolethalus syndrome 1
|
[NCBI]
|
7.46973e-05
|
|
|
|
plasminogen deficiency, type i
|
[NCBI]
|
7.21069e-05
|
|
|
|
POMT1
|
[NCBI]
|
7.06867e-05
|
|
|
|
cutis laxa, autosomal recessive, type ii
|
[NCBI]
|
6.98767e-05
|
|
|
|
SLSN1
|
[NCBI]
|
6.38696e-05
|
|
|
|
ACLS
|
[NCBI]
|
6.18557e-05
|
|
|
|
hypertelorism with esophageal abnormality and hypospadias
|
[NCBI]
|
5.57766e-05
|
|
|
|
EVC
|
[NCBI]
|
5.5243e-05
|
|
|
|
CDG1A
|
[NCBI]
|
5.15507e-05
|
|
|
|
PLG
|
[NCBI]
|
4.63808e-05
|
|
|
|
SLOS
|
[NCBI]
|
2.78809e-05
|
|
|
|
HGF
|
[NCBI]
|
2.32316e-05
|
|
