MeSH Browser

MeSH Supplementary: Holoprosencephaly 10
Unique ID: C567278
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567278
Entry Term(s): Holoprosencephaly with Microphthalmia and First Branchial Arch Anomalies
Registry Numbers: 0
Heading Mapped to: Branchial Region / abnormalities; *Chromosome Deletion; Chromosomes, Human, Pair 1; *Microphthalmos; *Holoprosencephaly; *Facies
Frequency: 1
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Holoprosencephaly 10 MeSH Supplementary Concept Data 2025