Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Porphobilinogen Synthase	[NCBI]

Gene	Link	Information Gain
ALAD	[NCBI]	0.000167957
PPOX	[NCBI]	1.35845e-05
VDR	[NCBI]	1.30484e-05
FAH	[NCBI]	1.25131e-05
CAT	[NCBI]	6.4548e-06
NOS3	[NCBI]	3.8935e-06
ACHE	[NCBI]	3.16795e-06
PON1	[NCBI]	2.19452e-06
AK1	[NCBI]	1.73978e-06
UROS	[NCBI]	1.71545e-06
GPT	[NCBI]	1.70038e-06
ALAS2	[NCBI]	1.62438e-06
HFE2	[NCBI]	1.50257e-06
HMBS	[NCBI]	1.46064e-06
NFE2	[NCBI]	1.37465e-06
HEBP1	[NCBI]	1.34989e-06
TYRP1	[NCBI]	1.20588e-06
GATA1	[NCBI]	1.02874e-06
CP	[NCBI]	1.02583e-06
G6PD	[NCBI]	7.70739e-07
MPO	[NCBI]	5.24711e-07

OMIM	Link	Information gain
ALAD	[NCBI]	0.0023028
porphyria variegata	[NCBI]	0.000348398
craniofacial dysmorphism with ocular coloboma, absent corpus callosum, and aortic dilatation	[NCBI]	0.000206042
MLASA	[NCBI]	0.000149036
hydroxyacyl-coa dehydrogenase ii deficiency	[NCBI]	0.000140636
HMBS	[NCBI]	0.000119431
VDR	[NCBI]	0.000112866
porphyria, acute intermittent	[NCBI]	9.06744e-05
tyrosinemia, type i	[NCBI]	9.01876e-05
danubian endemic familial nephropathy	[NCBI]	8.7436e-05
coproporphyria	[NCBI]	7.01277e-05
CAT	[NCBI]	3.86587e-05
PUS1	[NCBI]	2.93245e-05
CMPK1	[NCBI]	2.27117e-05
UROS	[NCBI]	2.02759e-05
AK1	[NCBI]	1.8163e-05
ACHE	[NCBI]	7.50675e-06
CP	[NCBI]	5.83241e-06
G6PD	[NCBI]	1.28568e-06
AVP	[NCBI]	4.21679e-07
MPO	[NCBI]	3.95193e-09