JSON

acromelanosis

^ http://purl.obolibrary.org/obo/MONDO_0018311

Acromelanosis is a congenital hyperpigmentation of the skin usually located on the acral areas of the fingers and toes. It is mostly observed in newborns or during the first years of life. [ Orphanet:39 ]

Term info

database cross reference
  • GARD:0004500 (MONDO:equivalentTo)
  • ICD9:709.09 (MONDO:relatedTo)
  • Orphanet:39 (MONDO:equivalentTo)
  • SCTID:239089006 (MONDO:equivalentTo)
Subsets

gard_rare, ordo_disease

definition

Acromelanosis is a congenital hyperpigmentation of the skin usually located on the acral areas of the fingers and toes. It is mostly observed in newborns or during the first years of life.

exactMatch

http://identifiers.org/snomedct/239089006, http://purl.obolibrary.org/obo/Orphanet_39

has related synonym

progressive acromelanosis

id

MONDO:0018311

seeAlso

https://rarediseases.info.nih.gov/diseases/4500/acromelanosis

Term relations