Search Ontology:
Human Disease

primary localized cutaneous amyloidosis 1

Term ID
DOID:0080930
Synonyms
  • familial primary localized cutaneous amyloidosis-1
Definition
A primary cutaneous amyloidosis that has_material_basis_in heterozygous mutation in the gene encoding oncostatin M receptor-beta (OSMR) on chromosome 5p13. https://pubmed.ncbi.nlm.nih.gov/19663869/
References
Ontology
Human Disease   ( DOID:0080930 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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