Homocystinuria without methylmalonic aciduria (Q89149): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed label, description and/or aliases in pt-br, en |
||
| description / pt-br | description / pt-br | ||
Homocistinúria sem acidúria metilmalônica é um erro inato do metabolismo da vitamina B12, caracterizado por anemia megaloblástica, encefalopatia e, às vezes, atraso no desenvolvimento, e está associado à homocistinúria e hiper-homocisteinemia. | |||
| description / en | description / en | ||
Homocystinuria without methylmalonic aciduria is an inborn error of vitamin B12 (cobalamin) metabolism characterised by megaloblastic anaemia, encephalopathy and, sometimes, developmental delay, and associated with homocystinuria and hyperhomocysteinaemia. | |||
Revision as of 15:42, 15 August 2026
Homocystinuria without methylmalonic aciduria is an inborn error of vitamin B12 (cobalamin) metabolism characterised by megaloblastic anaemia, encephalopathy and, sometimes, developmental delay, and associated with homocystinuria and hyperhomocysteinaemia.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_726186034 |
||
| English | Homocystinuria without methylmalonic aciduria |
Homocystinuria without methylmalonic aciduria is an inborn error of vitamin B12 (cobalamin) metabolism characterised by megaloblastic anaemia, encephalopathy and, sometimes, developmental delay, and associated with homocystinuria and hyperhomocysteinaemia. |
