MeSH Browser

MeSH Supplementary: Insulin-Like Growth Factor I Deficiency
Unique ID: C563867
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563867
Entry Term(s): Growth Retardation with Sensorineural Deafness and Mental Retardation; IGF1 Deficiency
Registry Numbers: 0
Heading Mapped to: *Growth Disorders; *Hearing Loss, Sensorineural; Insulin-Like Growth Factor I / deficiency
Frequency: 23
Note: mutation in IGF1
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Insulin-Like Growth Factor I Deficiency MeSH Supplementary Concept Data 2025