Hypoparathyroidism by glial cells missing B mutations (Q98058): Difference between revisions
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15 August 2026
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Latest revision as of 14:19, 16 August 2026
GCMB is a transcription factor which have essential role in the development of parathyroid hormone. Both autosomal dominant and recessive forms of familial hypoparathyroidism due to mutations in GCMB gene have been reported. (OMIM #146200)
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_153432885 |
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| English | Hypoparathyroidism by glial cells missing B mutations |
GCMB is a transcription factor which have essential role in the development of parathyroid hormone. Both autosomal dominant and recessive forms of familial hypoparathyroidism due to mutations in GCMB gene have been reported. (OMIM #146200) |
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CID11:ID_153432885
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dki-india-ID_153432885
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Concluído
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15 August 2026
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