|
OMIM |
Link |
Information gain |
01 |
|
HSCR1
|
[NCBI]
|
0.0116958
|
|
|
HSCR9
|
[NCBI]
|
0.00342502
|
|
|
RET
|
[NCBI]
|
0.00239718
|
|
|
mowat-wilson syndrome
|
[NCBI]
|
0.00134837
|
|
|
EDNRB
|
[NCBI]
|
0.00118643
|
|
|
waardenburg-shah syndrome
|
[NCBI]
|
0.00113449
|
|
|
HSCR7
|
[NCBI]
|
0.00111789
|
|
|
HSCR6
|
[NCBI]
|
0.00111789
|
|
|
HSCR5
|
[NCBI]
|
0.00111789
|
|
|
HSCR8
|
[NCBI]
|
0.00111789
|
|
|
HSCR2
|
[NCBI]
|
0.00111266
|
|
|
ACHE
|
[NCBI]
|
0.00110358
|
|
|
EDN3
|
[NCBI]
|
0.000941279
|
|
|
GDNF
|
[NCBI]
|
0.000753583
|
|
|
SOX10
|
[NCBI]
|
0.000739638
|
|
|
ZEB2
|
[NCBI]
|
0.000627761
|
|
|
visceral neuropathy, familial, autosomal recessive
|
[NCBI]
|
0.000625244
|
|
|
goldberg-shprintzen megacolon syndrome
|
[NCBI]
|
0.000554724
|
|
|
autonomic control, congenital failure of
|
[NCBI]
|
0.000430059
|
|
|
SRS
|
[NCBI]
|
0.000217145
|
|
|
VIP
|
[NCBI]
|
0.000197943
|
|
|
neuronal intestinal dysplasia, type b
|
[NCBI]
|
0.000169137
|
|
|
abcd syndrome
|
[NCBI]
|
0.000169137
|
|
|
PHOX2B
|
[NCBI]
|
0.00016206
|
|
|
PCWH
|
[NCBI]
|
0.000155181
|
|
|
L1CAM
|
[NCBI]
|
0.000132431
|
|
|
WS2A
|
[NCBI]
|
0.000107388
|
|
|
GFRA1
|
[NCBI]
|
0.000101898
|
|
|
hirschsprung disease with heart defects, laryngeal anomalies, and preaxial polydactyly
|
[NCBI]
|
9.99857e-05
|
|
|
hirschsprung disease with polydactyly, renal agenesis, and deafness
|
[NCBI]
|
9.99857e-05
|
|
|
hirschsprung disease with hypoplastic nails and dysmorphic facial features
|
[NCBI]
|
9.99857e-05
|
|
|
brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, hirschsprung disease, ear/eye anomalies, cleft palate/cryptorchidism, and kidney dysplasia/hypoplasia
|
[NCBI]
|
9.99857e-05
|
|
|
hirschsprung disease with type d brachydactyly
|
[NCBI]
|
9.99857e-05
|
|
|
WS2E
|
[NCBI]
|
9.99857e-05
|
|
|
SLOS
|
[NCBI]
|
8.33253e-05
|
|
|
NKX2-1
|
[NCBI]
|
7.10697e-05
|
|
|
corpus callosum, partial agenesis of, x-linked
|
[NCBI]
|
6.90987e-05
|
|
|
GFRA3
|
[NCBI]
|
6.46921e-05
|
|
|
FRS2
|
[NCBI]
|
6.46921e-05
|
|
|
KIAA1279
|
[NCBI]
|
6.46921e-05
|
|
|
CHH
|
[NCBI]
|
5.4272e-05
|
|
|
intestinal pseudoobstruction, neuronal, chronic idiopathic, x-linked
|
[NCBI]
|
5.13618e-05
|
|
|
GFRA2
|
[NCBI]
|
5.09261e-05
|
|
|
protoporphyria, erythropoietic
|
[NCBI]
|
4.58974e-05
|
|
|
NRTN
|
[NCBI]
|
4.57395e-05
|
|
|
PYY
|
[NCBI]
|
4.25372e-05
|
|
|
NPY
|
[NCBI]
|
4.25298e-05
|
|
|
currarino syndrome
|
[NCBI]
|
4.20286e-05
|
|
|
NGFR
|
[NCBI]
|
3.83345e-05
|
|
|
G22P1
|
[NCBI]
|
3.78927e-05
|
|
|
BBS
|
[NCBI]
|
3.73093e-05
|
|
|
ECE1
|
[NCBI]
|
3.48328e-05
|
|
|
AFD1
|
[NCBI]
|
3.40507e-05
|
|
|
BCHE
|
[NCBI]
|
3.11557e-05
|
|
|
OPTB1
|
[NCBI]
|
3.09669e-05
|
|
|
MKKS
|
[NCBI]
|
2.93901e-05
|
|
|
ADCYAP1
|
[NCBI]
|
2.81841e-05
|
|
|
SPG3A
|
[NCBI]
|
2.55035e-05
|
|
|
CES
|
[NCBI]
|
2.16102e-05
|
|
|
neuroblastoma
|
[NCBI]
|
2.13323e-05
|
|
|
ERBB2
|
[NCBI]
|
2.03331e-05
|
|
|
ITGB2
|
[NCBI]
|
1.9271e-05
|
|
|
RSTS
|
[NCBI]
|
1.90728e-05
|
|
|
ESD
|
[NCBI]
|
1.90242e-05
|
|
|
ALGS1
|
[NCBI]
|
1.73619e-05
|
|
|
PAX3
|
[NCBI]
|
1.48568e-05
|
|
|
ASS
|
[NCBI]
|
1.36115e-05
|
|
|
GAL
|
[NCBI]
|
9.46081e-06
|
|
|
TH
|
[NCBI]
|
8.67584e-06
|
|
|
HPS
|
[NCBI]
|
7.36936e-06
|
|
|
CHS
|
[NCBI]
|
4.63646e-06
|
|
|
NGFB
|
[NCBI]
|
3.56822e-06
|
|
|
BDNF
|
[NCBI]
|
1.72213e-06
|
|
|
APC
|
[NCBI]
|
9.64356e-07
|
|
|
GFAP
|
[NCBI]
|
8.20814e-07
|
|
|
CHAT
|
[NCBI]
|
1.57194e-08
|
|