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MeSH keywords -> Related genes, diseases (OMIM)


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01 Porphobilinogen Synthase [NCBI]


Gene


Gene Link Information
Gain
01
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


OMIM Link Information
gain
01
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




Database Center for Life Science