malignant atrophic papulosis
Malignant atrophic papulosis (MAP) is a rare, chronic, thrombo-obliterative vasculopathy characterized by papular skin lesions with central porcelain-white atrophy and a surrounding teleangiectatic rim. Systemic lesions may affect the gastrointestinal tract and the central nervous system (CNS) and are potentially lethal. [ Orphanet:679 ]
Term info
- MESH:D054853 (Orphanet:679/e)
- SCTID:400171002 (MONDO:equivalentTo)
- Orphanet:679 (OMIM:602248)
- ICD9:447.8 (MONDO:relatedTo)
- OMIM:602248 (Orphanet:679/e)
- MedDRA:10064281 (Orphanet:679/e)
- UMLS:C0221011 (Orphanet:679/e)
- GARD:0006249 (MONDO:equivalentTo)
- NCIT:C84835 (MONDO:equivalentTo)
ordo_disease
http://identifiers.org/meddra/10064281
Malignant atrophic papulosis (MAP) is a rare, chronic, thrombo-obliterative vasculopathy characterized by papular skin lesions with central porcelain-white atrophy and a surrounding teleangiectatic rim. Systemic lesions may affect the gastrointestinal tract and the central nervous system (CNS) and are potentially lethal.
https://omim.org/entry/602248, http://purl.obolibrary.org/obo/NCIT_C84835, http://identifiers.org/mesh/D054853, http://linkedlifedata.com/resource/umls/id/C0221011, http://identifiers.org/snomedct/400171002, http://purl.obolibrary.org/obo/Orphanet_679
papulosis atrophican maligna, Köhlmeier-Degos disease, Kohlmeier-Degos-Delort-Tricort syndrome, Degos disease, Köhlmeier-Degos-Delort-Tricort syndrome, Kohlmeier-Degos disease, malignant atrophic papulosis
atrophic papulosis, malignant, Degos syndrome, papulosis, malignant atrophic, Degos's malignant atrophic papulosis
MONDO:0011208