MeSH Browser

MeSH Supplementary: Persistent Hyperplastic Primary Vitreous, Autosomal Recessive
Unique ID: C566966
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566966
Entry Term(s): Persistent Hyperplastic Primary Vitreous, Autosomal Dominant
Registry Numbers: 0
Heading Mapped to: *Eye Abnormalities; *Eye Diseases, Hereditary
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Persistent Hyperplastic Primary Vitreous, Autosomal Recessive MeSH Supplementary Concept Data 2025