Public Health Information Network Vocabulary Access and Distribution System (PHIN VADS)

Albinism (disorder) {15890002 , SNOMED-CT } Congenital deficiency of pigment of skin (disorder) {1953005 , SNOMED-CT } Congenital immunodeficiency disease (disorder) {36138009 , SNOMED-CT } Congenital malformation (disorder) {276654001 , SNOMED-CT } Disorder of pigmentation (disorder) {414032001 , SNOMED-CT } Disorder of tyrosine metabolism (disorder) {37200009 , SNOMED-CT } Hereditary disorder of immune system (disorder) {363138005 , SNOMED-CT } Hereditary disorder of the integument (disorder) {363185004 , SNOMED-CT } Immunodeficiency associated with multiple organ system abnormalities (disorder) {234641000 , SNOMED-CT } Site-specific disorder of skin (disorder) {238907001 , SNOMED-CT }