MeSH Browser

MeSH Supplementary: Arthrogryposis multiplex congenita whistling face
Unique ID: C538401
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538401
Entry Term(s): Arthrogryposis Multiplex Congenita With Whistling Face; Illium syndrome; Illum Syndrome; Lethal autosomal recessive arthrogryposis multiplex congenita with whistling face and calcifications of the nervous system
Registry Numbers: 0
Heading Mapped to: *Arthrogryposis; *Craniofacial Abnormalities
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 2012/12/01

Arthrogryposis multiplex congenita whistling face MeSH Supplementary Concept Data 2025