MeSH Browser

MeSH Supplementary: Cutis Laxa-Marfanoid Syndrome
Unique ID: C563639
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563639
Entry Term(s): Neonatal Cutis Laxa With Marfanoid Phenotype
Registry Number: 0
Heading Mapped to: *Cutis Laxa; *Infant, Newborn, Diseases; *Marfan Syndrome
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 2013/10/24

Cutis Laxa-Marfanoid Syndrome MeSH Supplementary Concept Data 2023