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MeSH keywords -> Related genes, diseases (OMIM)


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01 Porphyria, Acute Intermittent [NCBI]

Gene


 Gene Link Information
Gain		 01
HMBS [NCBI] 0.000931674
PPOX [NCBI] 7.24681e-05
H2AFX [NCBI] 1.10376e-05
FECH [NCBI] 7.79804e-06
UROD [NCBI] 7.73161e-06
NR1I3 [NCBI] 7.22777e-06
SDHD [NCBI] 6.83969e-06
CAT [NCBI] 2.50743e-06
EPO [NCBI] 1.53903e-06



OMIM


 OMIM Link Information
gain		 01
HMBS [NCBI] 0.00497489
porphyria, acute intermittent [NCBI] 0.00248946
porphyria variegata [NCBI] 0.000441169
coproporphyria [NCBI] 0.000121336
porphyria, congenital erythropoietic [NCBI] 6.02468e-05
myoclonic epilepsy of unverricht and lundborg [NCBI] 4.83921e-05
HNF4A [NCBI] 3.32887e-05
PPOX [NCBI] 3.21981e-05
SLE [NCBI] 2.6591e-05
CAT [NCBI] 1.15522e-06
EPO [NCBI] 1.28161e-07



Database Center for Life Science