MeSH Browser

MeSH Supplementary: Laron syndrome type 2
Unique ID: C537871
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C537871
Entry Term(s): Growth Hormone Insensitivity Due To Postreceptor Defect; Growth Hormone Insensitivity With Immunodeficiency; Laron syndrome due to postreceptor defect; Laron type dwarfism 2
Registry Number: 0
Heading Mapped to: *Laron Syndrome
Frequency: 2
Indexing Information: STAT5 Transcription Factor
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Laron syndrome type 2 MeSH Supplementary Concept Data 2024