MeSH Browser

MeSH Supplementary: Proud Syndrome
Unique ID: C563110
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563110
Entry Term(s): ACC With Abnormal Genitalia; Corpus Callosum, Agenesis of, with Abnormal Genitalia
Registry Number: 0
Heading Mapped to: *Intellectual Disability; *Urogenital Abnormalities; *Genetic Diseases, X-Linked; *Agenesis of Corpus Callosum
Frequency: 0
Note: mutation in ARX
Date of Entry: 2012/11/05

Proud Syndrome MeSH Supplementary Concept Data 2023