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MeSH keywords -> Related genes, diseases (OMIM)


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01 Anencephaly [NCBI]

Gene


 Gene Link Information
Gain		 01
AFP [NCBI] 0.000164935
ACHE [NCBI] 7.82792e-05
PRL [NCBI] 2.21678e-05
CYP2C8 [NCBI] 1.84604e-05
CYP2C9 [NCBI] 1.30694e-05
ALX1 [NCBI] 1.21534e-05
CKB [NCBI] 1.04876e-05
FOXN1 [NCBI] 9.81165e-06
SIX3 [NCBI] 9.00074e-06
MTHFR [NCBI] 8.03234e-06
MTRR [NCBI] 6.44883e-06
GFAP [NCBI] 6.36009e-06
GRP [NCBI] 5.56393e-06
CD99 [NCBI] 5.30945e-06
FOLR1 [NCBI] 4.74003e-06
TRH [NCBI] 3.27292e-06



OMIM


 OMIM Link Information
gain		 01
anencephaly [NCBI] 0.00676804
NLS [NCBI] 0.000959242
EPV [NCBI] 0.000725612
AFP [NCBI] 0.000604669
THAS [NCBI] 0.00051629
constricting bands, congenital [NCBI] 0.000461898
short rib-polydactyly syndrome, type ii [NCBI] 0.000440615
neural tube defects, x-linked [NCBI] 0.000356852
ACHE [NCBI] 0.000274104
aprosencephaly syndrome [NCBI] 0.000227167
ACLS [NCBI] 0.000167471
neural tube defects [NCBI] 0.000166201
homocystinuria due to deficiency of n(5,10)-methylenetetrahydrofolate reductase activity [NCBI] 0.000155672
gluteal muscles, absence of [NCBI] 0.000140314
median-ulnar nerve communications [NCBI] 0.000140314
HPE4 [NCBI] 9.65043e-05
FRA16A [NCBI] 8.31968e-05
pituitary dwarfism due to isolated growth hormone deficiency, autosomal dominant [NCBI] 8.19513e-05
neural tube defects, folate-sensitive [NCBI] 7.77539e-05
MTHFR [NCBI] 7.23128e-05
RIEG1 [NCBI] 7.0453e-05
CART1 [NCBI] 6.68676e-05
PRL [NCBI] 5.03668e-05
FOLR1 [NCBI] 4.94602e-05
PITX2 [NCBI] 3.85842e-05
OXT [NCBI] 3.02612e-05
BRCA1 [NCBI] 1.84616e-05
GNRH1 [NCBI] 1.37753e-05
GFAP [NCBI] 8.9643e-06



Database Center for Life Science