Disease #02767 (Susceptibility to severe cutaneous adverse reaction, OMIM:608579)

Official abbreviation -
Name Susceptibility to severe cutaneous adverse reaction
OMIM ID 608579
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 2 genes HLA-A, HLA-B
Associated tissues -
Disease features -
Remarks -