Atrophia maculosa varioliformis cutis, familial

Preferred Label : Atrophia maculosa varioliformis cutis, familial;

Symbol : AMVC;

CISMeF acronym : AMVC;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Varioliform macular atrophy of the skin;

Inheritance : ? Autosomal recessive;

Prefixed ID : 601341;

Details

Origin ID

601341;

UMLS CUI

C1832465;

Currated CISMeF NLP mapping
- atrophia maculosa varioliformis cutis, familial [MeSH concept]
- atrophia maculosa varioliformis cutis, familial [MeSH Supplementary Concept]
HPO term(s)
- Abnormality of the skin [HPO term]
- Autosomal recessive inheritance [HPO term]
- Macular atrophy [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- atrophia maculosa varioliformis cutis, familial [MeSH Supplementary Concept]
- atrophia maculosa varioliformis cutis, familial [MeSH concept]

Keyword's position in hierarchy(ies) :

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