Jaundice, familial obstructive, of infancy

Preferred Label : Jaundice, familial obstructive, of infancy;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : X-linked recessive;

Prefixed ID : 308600;

Details

Origin ID

308600;

UMLS CUI

C1839927;

Currated CISMeF NLP mapping
- jaundice, familial obstructive, of infancy [MeSH concept]
- jaundice, familial obstructive, of infancy [MeSH Supplementary Concept]
HPO term(s)
- Jaundice [HPO term]
- Neonatal hyperbilirubinemia [HPO term]
- X-linked recessive inheritance [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- jaundice, familial obstructive, of infancy [MeSH Supplementary Concept]
- jaundice, familial obstructive, of infancy [MeSH concept]

Keyword's position in hierarchy(ies) :

You can consult :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients