MeSH keywords -> Related genes, diseases (OMIM)
Query MeSH keywords list
01
Porphyrias
[NCBI]
Gene
Gene
Link
Information
Gain
01
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
OMIM
Link
Information
gain
01
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
Database Center for Life Science