Multiple carboxylase deficiency due to biotinidase deficiency (Q86004): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Canary Token | |||
dki-india-ID_1336432647 | |||
| Property / Canary Token: dki-india-ID_1336432647 / rank | |||
Normal rank | |||
Revision as of 11:22, 15 August 2026
Biotinidase deficiency is a late-onset form of multiple carboxylase deficiency (see this term), an inborn error of biotin metabolism that, if untreated, is characterised by seizures, breathing difficulties, hypotonia, skin rash, alopecia, hearing loss and delayed development.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1336432647 |
||
| English | Multiple carboxylase deficiency due to biotinidase deficiency |
Biotinidase deficiency is a late-onset form of multiple carboxylase deficiency (see this term), an inborn error of biotin metabolism that, if untreated, is characterised by seizures, breathing difficulties, hypotonia, skin rash, alopecia, hearing loss and delayed development. |
Statements
CID11:ID_1336432647
0 references
dki-india-ID_1336432647
0 references
