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MeSH keywords -> Related genes, diseases (OMIM)


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01 Refsum Disease [NCBI]

Gene


 Gene Link Information
Gain		 01
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


 OMIM Link Information
gain		 01
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



Database Center for Life Science