dominant primary localized cutaneous amyloidosis

Preferred Label : dominant primary localized cutaneous amyloidosis;

Origin ID

D6-94642;

UMLS CUI

C0268398;

Automatic exact mappings (from CISMeF team)
- X-linked reticulate pigmentary disorder [ORDO Disease]
Currated CISMeF NLP mapping
- Dominant primary localized cutaneous amyloidosis (disorder) [SNOMED CT concept]
- Familial lichen amyloidosis (disorder) [SNOMED CT concept]
- amyloidosis IX [MeSH concept]
- amyloidosis IX [MeSH Supplementary Concept]
ICD-10 exact mapping(s)
- Non-neuropathic heredofamilial amyloidosis [ICD-10 Sub-category (who)]
Metaterm(s)
- dermatology [CISMeF Metaterm]
- internal medicine [CISMeF Metaterm]
- metabolism [CISMeF Metaterm]
SNOMED CT concept
- Dominant primary localized cutaneous amyloidosis (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Amyloidosis, primary localized cutaneous, 1 [OMIM Phenotype]
- Dominant primary localized cutaneous amyloidosis (disorder) [SNOMED CT concept]
- Familial lichen amyloidosis (disorder) [SNOMED CT concept]
- amyloidosis IX [MeSH Supplementary Concept]
- amyloidosis IX [MeSH concept]