atrophia maculosa varioliformis cutis, familial

Preferred Label : atrophia maculosa varioliformis cutis, familial;

MeSH synonym : varioliform macular atrophy of the skin;

Origin ID

C563349;

UMLS CUI

C1832465;

Currated CISMeF NLP mapping
- Atrophia maculosa varioliformis cutis, familial [OMIM Phenotype]
MeSH term(s) associated for indexing
- skin diseases, genetic [MeSH Descriptor]
Record concept(s)
- atrophia maculosa varioliformis cutis, familial [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Atrophia maculosa varioliformis cutis, familial [OMIM Phenotype]