MeSH Browser

MeSH Supplementary: Hanhart syndrome
Unique ID: C535629
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C535629
Entry Term(s): Oromandibular limb hypogenesis complex
Heading Mapped to: *Abnormalities, Multiple; *Limb Deformities, Congenital; *Craniofacial Abnormalities
Frequency: 8
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Hanhart syndrome MeSH Supplementary Concept Data 2024