MeSH Browser

MeSH Supplementary: Juvenile Polyposis with Hereditary Hemorrhagic Telangiectasia
Unique ID: C563412
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563412
Entry Term(s): JPHHT Syndrome; JPSHHT; Juvenile Polyposis Hereditary Hemorrhagic Telangiectasia Syndrome; Polyposis, Generalized Juvenile, with Pulmonary Arteriovenous Malformation; Telangiectasia, Hereditary Hemorrhagic, with Juvenile Polyposis Coli
Registry Numbers: 0
Heading Mapped to: *Telangiectasia, Hereditary Hemorrhagic; *Intestinal Polyposis
Frequency: 10
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Juvenile Polyposis with Hereditary Hemorrhagic Telangiectasia MeSH Supplementary Concept Data 2025