Hypoparathyroidism by glial cells missing B mutations (Q98058): Difference between revisions
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GCMB é um fator de trasncrição que tem papel essencial no desenvolvimento do hormônio da paratireoide. Ambas formas autossômicas dominante e recessiva de hipoparatireoidismo familiar devido a mutação no gene GCMB tem sido reportadas. | |||||||||||||||
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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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| Property / Canonical URI: https://id.who.int/icd/entity/153432885 / rank | |||||||||||||||
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CID11:ID_153432885 | |||||||||||||||
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dki-india-ID_153432885 | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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15 August 2026
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| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
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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 |
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| 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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