Hypoparathyroidism by glial cells missing B mutations (Q98058): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed label, description and/or aliases in pt-br, en |
Changed an Item |
||
| Property / Canonical URI | |||
| Property / Canonical URI: https://id.who.int/icd/entity/153432885 / rank | |||
Normal rank | |||
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 |
||
| 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) |
