Milia, multiple eruptive

Preferred Label : Milia, multiple eruptive;

Symbol : MEM;

CISMeF acronym : MEM;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal dominant;

Prefixed ID : %157400;

Details

Origin ID

157400;

UMLS CUI

C0343079;

Currated CISMeF NLP mapping
- Multiple eruptive milia (disorder) [SNOMED CT concept]
- milia, multiple eruptive [MeSH concept]
- milia, multiple eruptive [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Milia [HPO term]
Semantic type(s)
- Neoplastic Process [UMLS semantic type]
UMLS correspondences (same concept)
- Multiple eruptive milia (disorder) [SNOMED CT concept]
- milia, multiple eruptive [MeSH Supplementary Concept]
- milia, multiple eruptive [MeSH concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients