MeSH Browser

MeSH Supplementary: Rhizomelic chondrodysplasia punctata, type 3
Unique ID: C537608
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537608
Entry Term(s): AGPS deficiency; Alkyldihydroxyacetonephosphate synthase deficiency; Alkylglycerone-Phosphate Synthase Deficiency
Registry Number: 0
Heading Mapped to: *Chondrodysplasia Punctata, Rhizomelic
Frequency: 3
Date of Entry: 2010/08/25
Revision Date: 2012/08/24

Rhizomelic chondrodysplasia punctata, type 3 MeSH Supplementary Concept Data 2024