Gendoo

MeSH keywords -> Related genes, diseases (OMIM)

01	Refsum Disease	[NCBI]

Gene	Link	Information Gain
PHYH	[NCBI]	0.000506204
PEX7	[NCBI]	5.5121e-05
SCP2	[NCBI]	3.22277e-05
ALDH3A2	[NCBI]	3.11552e-05
PHYHIP	[NCBI]	1.38769e-05
PEX26	[NCBI]	1.32935e-05
GLMN	[NCBI]	1.2514e-05
PXMP3	[NCBI]	1.22266e-05
FKBP4	[NCBI]	1.19805e-05
AGPS	[NCBI]	1.12461e-05
PEX6	[NCBI]	1.02537e-05
HSD17B4	[NCBI]	9.36086e-06
PEX1	[NCBI]	9.31187e-06
AMACR	[NCBI]	8.26236e-06
NTRK1	[NCBI]	8.11232e-06
SPAST	[NCBI]	7.01954e-06

OMIM	Link	Information gain
cerebrohepatorenal syndrome, variant types	[NCBI]	0.00266538
refsum disease	[NCBI]	0.00223254
refsum disease, infantile form	[NCBI]	0.00164138
RDPA	[NCBI]	0.00107364
PHYH	[NCBI]	0.000686686
ZS	[NCBI]	0.000562338
adrenoleukodystrophy, autosomal neonatal form	[NCBI]	0.000413998
PXMP3	[NCBI]	0.000385833
ALD	[NCBI]	0.000262738
PEX7	[NCBI]	0.000198588
PHYHIP	[NCBI]	0.000179981
PEX6	[NCBI]	0.000135268
PBD	[NCBI]	0.000127906
KSS	[NCBI]	0.000119353
RCDP1	[NCBI]	0.000112078
FKBP4	[NCBI]	8.96982e-05
RCDP2	[NCBI]	7.50102e-05
ichthyosiform erythroderma, corneal involvement, and deafness	[NCBI]	7.23063e-05
hyperpipecolatemia	[NCBI]	6.99932e-05
ABCD3	[NCBI]	6.4831e-05
NCIE1	[NCBI]	5.83006e-05
keratitis-ichthyosis-deafness syndrome, autosomal dominant	[NCBI]	5.63538e-05
SPG2	[NCBI]	5.382e-05
NTRK1	[NCBI]	4.4889e-05
ALDH3A2	[NCBI]	4.43149e-05
CMT1B	[NCBI]	3.77647e-05