pigmentary disorder, reticulate, with systemic manifestations

Preferred Label : pigmentary disorder, reticulate, with systemic manifestations;

MeSH synonym : amyloidosis, familial cutaneous;

Origin ID

C564461;

UMLS CUI

C1845050;

Currated CISMeF NLP mapping
- Pigmentary disorder, reticulate, with systemic manifestations, X-linked [OMIM Phenotype]
- X-linked reticulate pigmentary disorder [ORDO Disease]
- X-linked reticulate pigmentary disorder with systemic manifestation syndrome (disorder) [SNOMED CT concept]
DO Cross reference
- X-linked reticulate pigmentary disorder [DO Concept]
MeSH term(s) associated for indexing
- amyloidosis, familial [MeSH Descriptor]
- genetic diseases, X-linked [MeSH Descriptor]
- pigmentation disorders [MeSH Descriptor]
- skin diseases, genetic [MeSH Descriptor]
Record concept(s)
- pigmentary disorder, reticulate, with systemic manifestations [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Pigmentary disorder, reticulate, with systemic manifestations, X-linked [OMIM Phenotype]
- X-linked reticulate pigmentary disorder [DO Concept]
- X-linked reticulate pigmentary disorder with systemic manifestation syndrome (disorder) [SNOMED CT concept]