Methylmalonic aciduria - homocystinuria type cbl D (Q101508): Difference between revisions
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Revision as of 18:19, 16 August 2026
cblD type methylmalonic acidemia with homocystinuria is a form of methylmalonic acidemia with homocystinuria, an inborn error of vitamin B12 (cobalamin) metabolism characterised by variable biochemical, neurological and haematological manifestations.
| Language | Label | Description | Also known as |
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| default for all languages | ID_615560358 |
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| English | Methylmalonic aciduria - homocystinuria type cbl D |
cblD type methylmalonic acidemia with homocystinuria is a form of methylmalonic acidemia with homocystinuria, an inborn error of vitamin B12 (cobalamin) metabolism characterised by variable biochemical, neurological and haematological manifestations. |
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CID11:ID_615560358
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dki-india-ID_615560358
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Concluído
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