Keratosis, familial actinic

Preferred Label : Keratosis, familial actinic;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 148390;

Details

Origin ID

148390;

UMLS CUI

C2675099;

Currated CISMeF NLP mapping
- keratosis, familial actinic [MeSH concept]
- keratosis, familial actinic [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- keratosis, familial actinic [MeSH Supplementary Concept]
- keratosis, familial actinic [MeSH concept]

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