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Disease Methylmalonic Aciduria and Homocystinuria, CblF Type

Name Methylmalonic Aciduria and Homocystinuria, CblF Type
Synonyms cblF | Cobalamin, Defect in Lysosomal Release of | Cobalamin F Disease | Methylmalonic Acidemia and Homocystinuria, CblF Type | Methylmalonic Aciduria due to Vitamin B12-Release Defect | Vitamin B12 Lysosomal Release Defect | Vitamin B12 Storage Disease
Categories Genetic disease (inborn) | Metabolic disease
MeSH® ID C564747
OMIM® ID 277380

Top ↑ Ancestors

1. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated exposure references Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated exposure references Amino Acid Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated exposure references Methylmalonic Aciduria and Homocystinuria, CblF Type Has associated chemicals Has associated genes
2. DiseasesNutritional and Metabolic Diseases Has associated chemicals Has associated genes Has associated exposure references Metabolic Diseases Has associated chemicals Has associated genes Has associated exposure references Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated exposure references Amino Acid Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated exposure references Methylmalonic Aciduria and Homocystinuria, CblF Type Has associated chemicals Has associated genes

Top ↑ Descendants

None.