MeSH Browser

MeSH Supplementary: Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract
Unique ID: C567203
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567203
Registry Numbers: 0
Heading Mapped to: *Ataxia; *Cataract; *Polyneuropathies; *Retinitis Pigmentosa
Frequency: 14
Note: mutation on ABHD12 protein, human
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract MeSH Supplementary Concept Data 2025