Familial isolated hypoparathyroidism (Q56223): 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/1079633828 / rank | |||
Normal rank | |||
Revision as of 03:54, 14 August 2026
Familial isolated hypoparathyroidism is a rare heterogeneous group of metabolic disorders characterised by abnormal calcium metabolism due to deficient secretion of parathormone (PTH), without other endocrine disorders or developmental defects, with autosomal dominant or recessive inheritance.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1079633828 |
||
| English | Familial isolated hypoparathyroidism |
Familial isolated hypoparathyroidism is a rare heterogeneous group of metabolic disorders characterised by abnormal calcium metabolism due to deficient secretion of parathormone (PTH), without other endocrine disorders or developmental defects, with autosomal dominant or recessive inheritance. |
