MeSH Browser

MeSH Supplementary: Acrootoocular Syndrome
Unique ID: C564866
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564866
Entry Term(s): Pseudopapilledema, Ocular Hypotelorism, Blepharophimosis, and Hand Anomalies
Registry Number: 0
Heading Mapped to: *Foot Deformities, Congenital; *Hand Deformities, Congenital; *Hearing Loss, Sensorineural; *Hypertelorism; *Eye Diseases, Hereditary; *Blepharophimosis
Frequency: 0
Date of Entry: 2012/11/05

Acrootoocular Syndrome MeSH Supplementary Concept Data 2023