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Parent Node:
expandskin disease (MONDO:0005093)
..Starting node
..expandmongolian spot ()

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MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:6582
Name:mongolian spot
Definition:A benign, flat, congenital birthmark, with wavy borders and an irregular shape. The colour is caused by melanocytes, melanin-containing cells, that are usually located in the surface of the skin (the epidermis), but are in the deeper region (the dermis) in the location of the spot.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:blue sacral spot; congenital dermal melanocytosis; Mongolian macula
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
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Phenotypes
Disease Causing ClinVar Variants
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