Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Porphyrias	[NCBI]

Gene	Link	Information Gain
PORC	[NCBI]	0.000499621
PPOX	[NCBI]	0.000416009
UROD	[NCBI]	0.000242996
HMBS	[NCBI]	0.000121545
FECH	[NCBI]	8.83324e-05
UROS	[NCBI]	3.14902e-05
ALAD	[NCBI]	2.99807e-05
CPOX	[NCBI]	2.0135e-05
ALAS1	[NCBI]	1.14308e-05
RBP2	[NCBI]	1.10852e-05
TST	[NCBI]	1.05519e-05
AHR	[NCBI]	1.04208e-05
ERAF	[NCBI]	9.42017e-06
HEBP1	[NCBI]	9.19857e-06
ALAS2	[NCBI]	7.93502e-06
HFE	[NCBI]	6.11007e-06
PPARGC1A	[NCBI]	5.57922e-06
FAH	[NCBI]	5.47197e-06
CYP2D6	[NCBI]	5.02891e-06
ABCG2	[NCBI]	3.96421e-06
CYP3A4	[NCBI]	3.69125e-06
SHBG	[NCBI]	3.06052e-06
ACHE	[NCBI]	1.94984e-06
NGF	[NCBI]	1.12774e-06

OMIM	Link	Information gain
porphyria, acute intermittent	[NCBI]	0.00427201
porphyria variegata	[NCBI]	0.00332128
porphyria cutanea tarda	[NCBI]	0.00288407
porphyria, congenital erythropoietic	[NCBI]	0.00181313
protoporphyria, erythropoietic	[NCBI]	0.00180429
ALAD	[NCBI]	0.00108747
coproporphyria	[NCBI]	0.000839996
porphyria cutanea tarda, type i	[NCBI]	0.000752337
HMBS	[NCBI]	0.000678616
PPOX	[NCBI]	0.00032092
RA	[NCBI]	0.000225683
UROS	[NCBI]	0.000123101
spinal muscular atrophy with mental retardation	[NCBI]	0.000107066
SLE	[NCBI]	9.56003e-05
craniofacial dysmorphism with ocular coloboma, absent corpus callosum, and aortic dilatation	[NCBI]	8.46155e-05
CYP1A1	[NCBI]	8.09407e-05
syringomas, multiple	[NCBI]	7.61552e-05
hydroxyacyl-coa dehydrogenase ii deficiency	[NCBI]	6.06599e-05
CMD3B	[NCBI]	5.01789e-05
GVM	[NCBI]	4.67559e-05
lipoid proteinosis of urbach and wiethe	[NCBI]	3.95294e-05
FCAS	[NCBI]	3.37576e-05
DJS	[NCBI]	2.92995e-05
AHR	[NCBI]	2.01813e-05
tyrosinemia, type i	[NCBI]	1.73834e-05
DMD	[NCBI]	8.14666e-06
HFE	[NCBI]	7.55038e-06
NGFB	[NCBI]	5.13806e-06
AVP	[NCBI]	3.30627e-06
SHBG	[NCBI]	8.47069e-07
HD	[NCBI]	6.71233e-07
ACHE	[NCBI]	4.50081e-07