Dermal ridges, nelson syndrome

Preferred Label : Dermal ridges, nelson syndrome;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 125530;

Details

Origin ID

125530;

UMLS CUI

C1852161;

Currated CISMeF NLP mapping
- dermal ridges, nelson syndrome [MeSH concept]
- dermal ridges, nelson syndrome [MeSH Supplementary Concept]
HPO term(s)
- Abnormal dermatoglyphics [HPO term]
- Autosomal dominant inheritance [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- dermal ridges, nelson syndrome [MeSH Supplementary Concept]
- dermal ridges, nelson syndrome [MeSH concept]

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