MeSH Browser

MeSH Supplementary: Incontinentia pigmenti, familial male-lethal type
Unique ID: C531716
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C531716
Registry Numbers: 0
Heading Mapped to: *Incontinentia Pigmenti
Frequency: 108
Note: An X-linked dominant disorder that is usually prenatally lethal in males. It is caused by mutations in the IKBKG gene. OMIM: 308300
Date of Entry: 2010/08/25
Revision Date: 2016/07/11

Incontinentia pigmenti, familial male-lethal type MeSH Supplementary Concept Data 2025