MeSH Browser

MeSH Supplementary: Cutis Laxa, Autosomal Recessive, Type IIA
Unique ID: C562632
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562632
Entry Term(s): ARCL2A; Cutis Laxa With Bone Dystrophy; Cutis Laxa With Growth And Developmental Delay; Cutis Laxa With Joint Laxity And Retarded Development; Cutis Laxa With Or Without Congenital Disorder Of Glycosylation; Cutis Laxa, Debre Type
Registry Numbers: 0
Heading Mapped to: *Cutis Laxa
Frequency: 6
Note: PROM mutation in ATP6V0A2 gene
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Cutis Laxa, Autosomal Recessive, Type IIA MeSH Supplementary Concept Data 2025