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MeSH keywords -> Related genes, diseases (OMIM)


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01 Facial Asymmetry [NCBI]

Gene


 Gene Link Information
Gain		 01
HFM [NCBI] 0.0140371
ACF [NCBI] 0.000458595
FAM58A [NCBI] 1.63379e-05
HRAS [NCBI] 1.23356e-05
TPM2 [NCBI] 1.22954e-05
SALL4 [NCBI] 1.15809e-05
OPHN1 [NCBI] 1.15809e-05
CHD7 [NCBI] 1.15093e-05
PFN1 [NCBI] 1.11333e-05
SALL1 [NCBI] 1.08251e-05
AMPD1 [NCBI] 1.07336e-05
EYA1 [NCBI] 9.87506e-06
DNMT3B [NCBI] 9.62424e-06
ADH1B [NCBI] 8.55066e-06
FGFR3 [NCBI] 6.38454e-06
CD68 [NCBI] 4.59677e-06
PTH [NCBI] 2.89076e-06



OMIM


 OMIM Link Information
gain		 01
HFM [NCBI] 0.0320016
cayler cardiofacial syndrome [NCBI] 0.00319695
hemifacial microsomia with radial defects [NCBI] 0.00175016
proteus syndrome [NCBI] 0.000577283
HFH [NCBI] 0.000540115
HFA [NCBI] 0.00040697
oculodentoosseous dysplasia, recessive [NCBI] 0.00040697
microtia-anotia [NCBI] 0.000368517
dysgnathia complex [NCBI] 0.000368517
auriculocondylar syndrome [NCBI] 0.000368517
rokitansky-kuster-hauser syndrome [NCBI] 0.000314952
camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases [NCBI] 0.00031308
hairy elbows [NCBI] 0.000291817
HTC1 [NCBI] 0.000273386
microtia with meatal atresia and conductive deafness [NCBI] 0.000273386
hemifacial myohyperplasia [NCBI] 0.000266456
kenny-caffey syndrome, type 2 [NCBI] 0.000242681
dandy-walker-like malformation with atrioventricular septal defect [NCBI] 0.000156788
DA2A [NCBI] 0.000142322
TBS [NCBI] 0.000140477
deafness-craniofacial syndrome [NCBI] 0.00013289
speech development, delayed, with facial asymmetry, strabismus, and transverse earlobe crease [NCBI] 0.00013289
facial asymmetry [NCBI] 0.00013289
stratton-parker syndrome [NCBI] 0.000110422
contractures, congenital, torticollis, and malignant hyperthermia [NCBI] 0.000110422
MBS [NCBI] 9.30604e-05
mental retardation, x-linked, with cerebellar hypoplasia and distinctive facial appearance [NCBI] 9.23488e-05
poland syndrome [NCBI] 8.9573e-05
hyperpipecolatemia [NCBI] 8.40597e-05
PFN1 [NCBI] 7.46818e-05
CHD7 [NCBI] 7.26806e-05
HSR [NCBI] 7.10164e-05
OPHN1 [NCBI] 6.83464e-05
AFD1 [NCBI] 6.63054e-05
SALL1 [NCBI] 6.53402e-05
SCDO1 [NCBI] 6.03874e-05
ODDD [NCBI] 5.89692e-05
charge syndrome [NCBI] 5.80894e-05
TCOF [NCBI] 4.89295e-05
velocardiofacial syndrome [NCBI] 4.82273e-05
ALGS1 [NCBI] 4.82273e-05
CDLS1 [NCBI] 4.00591e-05
FGFR3 [NCBI] 3.57117e-05
fragile x mental retardation syndrome [NCBI] 3.46763e-05
klippel-trenaunay-weber syndrome [NCBI] 1.64155e-05
PTH [NCBI] 9.14044e-06
SRS [NCBI] 3.72495e-08



Database Center for Life Science