MeSH Browser

MeSH Supplementary: Milner Khallouf Gibson syndrome
Unique ID: C537473
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537473
Registry Numbers: 0
Heading Mapped to: *Fanconi Anemia; *Growth Disorders; *Microcephaly; *Micrognathism; Nose / abnormalities; Thumb / abnormalities
Frequency: 0
Note: Microcephaly, short stature, slow growth, beak nose, micrognathia, skin dyspigmentation and forearm and thumb dysplasia
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Milner Khallouf Gibson syndrome MeSH Supplementary Concept Data 2025