MeSH Browser

MeSH Supplementary: Radioulnar synostosis retinal pigment abnormalities
Unique ID: C536270
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536270
Registry Numbers: 0
Heading Mapped to: *Growth Disorders; *Intellectual Disability; *Retinitis Pigmentosa; *Synostosis; *Facies
Frequency: 0
Source: Genet Couns. 1991;2(4):237-40
Date of Entry: 2010/08/25
Revision Date: 1955/01/01

Radioulnar synostosis retinal pigment abnormalities MeSH Supplementary Concept Data 2025