MeSH Browser

MeSH Supplementary: Telfer Sugar Jaeger syndrome
Unique ID: C536955
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536955
Entry Term(s): Piebald trait neurologic defects; White forelock and leukoderma with neurological impairment
Registry Numbers: 0
Heading Mapped to: *Movement Disorders; *Piebaldism
Frequency: 0
Source: Am J Hum Genet. 1971;23(4):383-9
Date of Entry: 2010/08/25
Revision Date: 1955/01/01

Telfer Sugar Jaeger syndrome MeSH Supplementary Concept Data 2025