MeSH Browser

MeSH Supplementary: 17,20-Lyase Deficiency, Isolated
Unique ID: C567076
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567076
Entry Term(s): 17-Alpha-Hydroxylase-17,20-Lyase Deficiency, Combined Complete; 17-Alpha-Hydroxylase-17,20-Lyase Deficiency, Combined Partial
Registry Numbers: 0
Heading Mapped to: *Adrenal Hyperplasia, Congenital; Cytochrome P-450 Enzyme System / deficiency
Frequency: 2
Date of Entry: 2012/11/05
Revision Date: 2015/11/04

17,20-Lyase Deficiency, Isolated MeSH Supplementary Concept Data 2025