Catalog

Familial partial lipodystrophy associated with PLIN1 mutations

No MMS code

Link to WHO Definition

Familial partial lipodystrophy associated with PLIN1 mutations – http://id.who.int/icd/entity/98904071

This refers to an autosomal dominant skin condition characterised by the loss of subcutaneous fat. This diagnosis is associated with PLIN1 mutations.