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MeSH keywords -> Related genes, diseases (OMIM)


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01 Fibromuscular Dysplasia [NCBI]

Gene


 Gene Link Information
Gain		 01
CD68 [NCBI] 1.3789e-05
SSTR4 [NCBI] 1.15557e-05
SERPINA1 [NCBI] 8.87554e-06
AGTR1 [NCBI] 8.10434e-06
AGT [NCBI] 7.15677e-06
ACE [NCBI] 6.08017e-06
ACHE [NCBI] 5.76409e-06
TGFB1 [NCBI] 4.96153e-06
BAX [NCBI] 4.9133e-06
PCNA [NCBI] 4.51124e-06
PTH [NCBI] 3.86605e-06



OMIM


 OMIM Link Information
gain		 01
fibromuscular dysplasia of arteries [NCBI] 0.000885733
arterial occlusive disease, progressive, with hypertension, heart defects, bone fragility, and brachysyndactyly [NCBI] 0.000122684
COL3A1 [NCBI] 0.000120973
internal carotid artery, spontaneous dissection of [NCBI] 0.000108698
aortic aneurysm, abdominal [NCBI] 7.52744e-05
ehlers-danlos syndrome, type iv, autosomal dominant [NCBI] 6.98416e-05
NF1 [NCBI] 3.38766e-05
ACHE [NCBI] 2.05458e-05
PCNA [NCBI] 1.38818e-05
PTH [NCBI] 1.05376e-05
VEGF [NCBI] 5.05168e-06
SLE [NCBI] 1.79638e-06



Database Center for Life Science