Methylmalonic aciduria - homocystinuria type cbl F (Q101516): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Canary Token | |||
dki-india-ID_680621786 | |||
| Property / Canary Token: dki-india-ID_680621786 / rank | |||
Normal rank | |||
Revision as of 18:20, 16 August 2026
cblF type methylmalonic acidemia with homocystinuria is a form of methylmalonic acidemia with homocystinuria, an inborn error of vitamin B12 (cobalamin) metabolism characterised by megaloblastic anaemia, lethargy, failure to thrive, developmental delay, intellectual deficit and seizures.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_680621786 |
||
| English | Methylmalonic aciduria - homocystinuria type cbl F |
cblF type methylmalonic acidemia with homocystinuria is a form of methylmalonic acidemia with homocystinuria, an inborn error of vitamin B12 (cobalamin) metabolism characterised by megaloblastic anaemia, lethargy, failure to thrive, developmental delay, intellectual deficit and seizures. |
Statements
CID11:ID_680621786
0 references
dki-india-ID_680621786
0 references
