Non-HFE-related hereditary haemochromatosis, Type 4 (Q97536): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed an Item |
||||||||||||||
| (6 intermediate revisions by the same user not shown) | |||||||||||||||
| description / pt-br | description / pt-br | ||||||||||||||
A hemocromatose tipo 4 (também chamada de doença da ferroportina) é uma forma rara de hemocromatose hereditária, um grupo de doenças de origem genética caracterizadas pela deposição excessiva de ferro nos tecidos. É fenotipicamente heterogênea com dois subtipos. A forma A da doença da ferroportina é a forma usual e geralmente assintomática, sem danos aos tecidos e outras complicações. A doença da ferroportina forma B é mais rara e se assemelha à hemocromatose tipo 1, mas pode afetar crianças. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Hemochromatosis type 4 (also called ferroportin disease) is a rare form of hereditary hemochromatosis, a group of diseases characterised by excessive tissue iron deposition of genetic origin. It is phenotypically heterogeneous with two sub-types. Ferroportin disease form A is the usual form and is generally asymptomatic with no tissue damage and further complications. Ferroportin disease form B is rarer and resembles hemochromatosis type 1, but can affect children. | |||||||||||||||
| Property / Canonical URI | |||||||||||||||
| Property / Canonical URI: https://id.who.int/icd/entity/1541297428 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / CURIE | |||||||||||||||
CID11:ID_1541297428 | |||||||||||||||
| Property / CURIE: CID11:ID_1541297428 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Canary Token | |||||||||||||||
dki-india-ID_1541297428 | |||||||||||||||
| Property / Canary Token: dki-india-ID_1541297428 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Verification Status | |||||||||||||||
Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Collection date | |||||||||||||||
15 August 2026
| |||||||||||||||
| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 13:39, 16 August 2026
Hemochromatosis type 4 (also called ferroportin disease) is a rare form of hereditary hemochromatosis, a group of diseases characterised by excessive tissue iron deposition of genetic origin. It is phenotypically heterogeneous with two sub-types. Ferroportin disease form A is the usual form and is generally asymptomatic with no tissue damage and further complications. Ferroportin disease form B is rarer and resembles hemochromatosis type 1, but can affect children.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1541297428 |
||
| English | Non-HFE-related hereditary haemochromatosis, Type 4 |
Hemochromatosis type 4 (also called ferroportin disease) is a rare form of hereditary hemochromatosis, a group of diseases characterised by excessive tissue iron deposition of genetic origin. It is phenotypically heterogeneous with two sub-types. Ferroportin disease form A is the usual form and is generally asymptomatic with no tissue damage and further complications. Ferroportin disease form B is rarer and resembles hemochromatosis type 1, but can affect children. |
Statements
CID11:ID_1541297428
0 references
dki-india-ID_1541297428
0 references
Concluído
0 references
15 August 2026
0 references
