MeSH Browser

MeSH Supplementary: Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia
Unique ID: C564519
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564519
Entry Term(s): Bresek Syndrome; Bresheck Syndrome
Registry Number: 0
Heading Mapped to: *Congenital Abnormalities; Brain / *abnormalities; Ear / *abnormalities; *Ectodermal Dysplasia; *Hirschsprung Disease; Kidney / *abnormalities; *Intellectual Disability; *Genetic Diseases, X-Linked
Frequency: 4
Date of Entry: 2012/11/05
Revision Date: 2015/11/09

Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia MeSH Supplementary Concept Data 2023