MeSH Browser

MeSH Supplementary: Pseudohypoparathyroidism Type 1B
Unique ID: C548075
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C548075
Registry Number: 0
Heading Mapped to: *Pseudohypoparathyroidism
Frequency: 59
Note: A form of pseudohypoparathyroidism that is associated with deletions in chromosome 20 region q13.32, which affect the STX16, GNASAS1, or GNAS genes. OMIM: 603233
Date of Entry: 2010/08/25
Revision Date: 2016/09/29

Pseudohypoparathyroidism Type 1B MeSH Supplementary Concept Data 2023