MeSH Browser

MeSH Supplementary: X-Linked Chondrodysplasia Punctata 1
Unique ID: C580533
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C580533
Entry Term(s): Arylsulfatase E Deficiency; CDXP1; Cdpx1; Chondrodysplasia Punctata 1, X-Linked; Chondrodysplasia punctata 1, X-linked recessive; X-Linked Recessive Chondrodysplasia Punctata 1
Heading Mapped to: *Chondrodysplasia Punctata; *Genetic Diseases, X-Linked
Frequency: 12
Date of Entry: 2013/10/24
Revision Date: 2021/10/19

X-Linked Chondrodysplasia Punctata 1 MeSH Supplementary Concept Data 2024