MeSH Browser

MeSH Supplementary: Slavotinek Pike Mills Hurst syndrome
Unique ID: C536672
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C536672
Registry Number: 0
Heading Mapped to: Bone and Bones / *abnormalities; Cataract / *congenital; *Growth Disorders; *Learning Disabilities
Frequency: 0
Note: Cataracts, motor system disorder, short stature, learning difficulties, and skeletal abnormalities
Source: Am J Med Genet. 1996;62(1):42-7
Date of Entry: 2010/08/25
Revision Date: 2013/11/06

Slavotinek Pike Mills Hurst syndrome MeSH Supplementary Concept Data 2024