View disease #00004

Official abbreviation Both
Name Both
OMIM ID -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 14 genes BCHE, C12orf10, CAT, DDR1, FOXP3, GPX1, IFNG, IRF4, MC1R, NLRP1, NR1H3, RNASET2, TYR, VDR