MeSH Browser

MeSH Supplementary: Polycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism, and Brachymelia
Unique ID: C564881
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564881
Heading Mapped to: *Abnormalities, Multiple; *Craniosynostoses; *Ectromelia; *Hypertelorism; *Polycystic Kidney, Autosomal Recessive
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Polycystic Kidney Disease, Potter Type I, with Microbrachycephaly, Hypertelorism, and Brachymelia MeSH Supplementary Concept Data 2024