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Metadata
ID DOID:0080932
Name primary localized cutaneous amyloidosis 3
Definition A primary cutaneous amyloidosis that is characterized by deposits of keratinocyte-derived amyloid in the skin and that has_material_basis_in homozygous or compound heterozygous mutation in the GPNMB gene on chromosome 7p15. Onset occurs before puberty and involves macular or reticulate hyperpigmentation admixed with symmetrically distributed guttate hypopigmented and hyperpigmented lesions.
https://pubmed.ncbi.nlm.nih.gov/25866143/
Xrefs

MIM:617920

Synonyms

Amyloidosis cutis dyschromica [EXACT]

Parent Relationships

is_a primary cutaneous amyloidosis

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