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Laron syndrome type 2 MeSH Supplementary Concept Data 2022


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 Preferred
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