Gendoo

MeSH keywords -> Related genes, diseases (OMIM)


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01 Oligohydramnios [NCBI]

Gene


 Gene Link Information
Gain		 01
AFP [NCBI] 4.83164e-05
PDGFA [NCBI] 1.60279e-05
PTGS2 [NCBI] 1.31868e-05
DHCR7 [NCBI] 9.97915e-06
GLB1 [NCBI] 9.90841e-06
REN [NCBI] 9.2778e-06
NPPB [NCBI] 8.10836e-06
EDN1 [NCBI] 7.50369e-06
SERPINA1 [NCBI] 7.45354e-06
HNF1B [NCBI] 6.53477e-06
PKD1 [NCBI] 6.10558e-06
AVP [NCBI] 4.33034e-06
IL1RN [NCBI] 4.03728e-06



OMIM


 OMIM Link Information
gain		 01
urogenital adysplasia, hereditary [NCBI] 0.00162787
short rib-polydactyly syndrome, type i [NCBI] 0.000647644
omodysplasia, generalized form [NCBI] 0.000605677
short rib-polydactyly syndrome, type iii [NCBI] 0.000572697
short rib-polydactyly syndrome, type iv [NCBI] 0.000545541
short rib-polydactyly syndrome, type ii [NCBI] 0.000512118
MRD [NCBI] 0.000502422
RTD [NCBI] 0.000447952
VUR1 [NCBI] 0.000441356
PCD [NCBI] 0.000418126
pena-shokeir syndrome, type i [NCBI] 0.000368318
AOS [NCBI] 0.000364525
AFP [NCBI] 0.000227279
fraser syndrome [NCBI] 7.79682e-05
MADD [NCBI] 7.79682e-05
gm1-gangliosidosis, type i [NCBI] 7.7463e-05
sotos syndrome [NCBI] 6.88211e-05
MME [NCBI] 5.79776e-05
AGT [NCBI] 5.0947e-05
SLOS [NCBI] 4.6699e-05
AVP [NCBI] 1.26953e-05



Database Center for Life Science