|
OMIM |
Link |
Information gain |
01 |
|
ehlers-danlos syndrome, type viii
|
[NCBI]
|
0.0100121
|
|
|
ehlers-danlos syndrome, type vib
|
[NCBI]
|
0.00469457
|
|
|
ehlers-danlos syndrome, type i
|
[NCBI]
|
0.00392288
|
|
|
ehlers-danlos syndrome, type iv, autosomal dominant
|
[NCBI]
|
0.00339845
|
|
|
ehlers-danlos syndrome, type v
|
[NCBI]
|
0.00290304
|
|
|
COL3A1
|
[NCBI]
|
0.00262154
|
|
|
ehlers-danlos syndrome, type vi
|
[NCBI]
|
0.00184289
|
|
|
PLOD1
|
[NCBI]
|
0.00132792
|
|
|
ehlers-danlos syndrome, type vii, autosomal dominant
|
[NCBI]
|
0.00122251
|
|
|
ehlers-danlos syndrome, type ii
|
[NCBI]
|
0.00122251
|
|
|
COL1A2
|
[NCBI]
|
0.00115866
|
|
|
ehlers-danlos syndrome, type vii, autosomal recessive
|
[NCBI]
|
0.000959149
|
|
|
cutis laxa, x-linked
|
[NCBI]
|
0.000942306
|
|
|
COL5A1
|
[NCBI]
|
0.000810713
|
|
|
joint laxity, familial
|
[NCBI]
|
0.000742078
|
|
|
ehlers-danlos syndrome, type iii
|
[NCBI]
|
0.0006342
|
|
|
marfanoid hypermobility syndrome
|
[NCBI]
|
0.0006095
|
|
|
dentin dysplasia, type i
|
[NCBI]
|
0.000567689
|
|
|
heterotopia, periventricular, ehlers-danlos variant
|
[NCBI]
|
0.00040595
|
|
|
TNXB
|
[NCBI]
|
0.000338763
|
|
|
menkes disease
|
[NCBI]
|
0.000319093
|
|
|
ehlers-danlos syndrome, autosomal recessive, cardiac valvular form
|
[NCBI]
|
0.000304319
|
|
|
ehlers-danlos-like syndrome due to tenascin-x deficiency
|
[NCBI]
|
0.000304319
|
|
|
COL1A1
|
[NCBI]
|
0.000286147
|
|
|
ATS
|
[NCBI]
|
0.000276149
|
|
|
aneurysm, intracranial berry, 1
|
[NCBI]
|
0.000261717
|
|
|
ATP7A
|
[NCBI]
|
0.000256904
|
|
|
ehlers-danlos syndrome, progeroid form
|
[NCBI]
|
0.000249831
|
|
|
ehlers-danlos syndrome with platelet dysfunction from fibronectin abnormality
|
[NCBI]
|
0.000202785
|
|
|
CF
|
[NCBI]
|
0.000148872
|
|
|
cutis laxa, autosomal dominant
|
[NCBI]
|
0.000107705
|
|
|
FLNA
|
[NCBI]
|
0.000107126
|
|
|
COL5A2
|
[NCBI]
|
0.000106721
|
|
|
ehlers-danlos syndrome, autosomal dominant, type unspecified
|
[NCBI]
|
0.000101345
|
|
|
ehlers-danlos syndrome, beasley-cohen type
|
[NCBI]
|
0.000101345
|
|
|
osteogenesis imperfecta, type i
|
[NCBI]
|
9.64572e-05
|
|
|
cutis laxa, autosomal recessive, type i
|
[NCBI]
|
9.63133e-05
|
|
|
DCN
|
[NCBI]
|
7.67367e-05
|
|
|
COL5A3
|
[NCBI]
|
7.00337e-05
|
|
|
ADAMTS14
|
[NCBI]
|
7.00337e-05
|
|
|
ADAMTS2
|
[NCBI]
|
7.00337e-05
|
|
|
furlong syndrome: fs
|
[NCBI]
|
6.49753e-05
|
|
|
angioid streaks
|
[NCBI]
|
6.09106e-05
|
|
|
B4GALT7
|
[NCBI]
|
5.62616e-05
|
|
|
ADAMTS1
|
[NCBI]
|
5.10688e-05
|
|
|
dentinogenesis imperfecta, shields type iii
|
[NCBI]
|
4.89277e-05
|
|
|
WSS
|
[NCBI]
|
4.58905e-05
|
|
|
LDS
|
[NCBI]
|
4.45693e-05
|
|
|
xanthinuria, type i
|
[NCBI]
|
4.11742e-05
|
|
|
DGI1
|
[NCBI]
|
4.11742e-05
|
|
|
osteoporosis, juvenile
|
[NCBI]
|
4.01916e-05
|
|
|
TGFBR1
|
[NCBI]
|
3.8894e-05
|
|
|
EPS
|
[NCBI]
|
3.60556e-05
|
|
|
UCMD
|
[NCBI]
|
3.46759e-05
|
|
|
BGN
|
[NCBI]
|
3.29783e-05
|
|
|
LCA1
|
[NCBI]
|
3.06672e-05
|
|
|
TGFBR2
|
[NCBI]
|
2.81147e-05
|
|
|
MFS
|
[NCBI]
|
2.1454e-05
|
|
|
aortic valve disease
|
[NCBI]
|
2.09821e-05
|
|
|
osteogenesis imperfecta, type iia
|
[NCBI]
|
2.07385e-05
|
|
|
ELN
|
[NCBI]
|
1.99851e-05
|
|
|
SVAS
|
[NCBI]
|
1.61581e-05
|
|
|
HHT
|
[NCBI]
|
1.47605e-05
|
|
|
PXE
|
[NCBI]
|
4.16399e-06
|
|
|
polycystic kidneys
|
[NCBI]
|
6.58793e-07
|
|