Skip to main content
Diseases

Methylmalonic Acidemia With Homocystinuria, Type Cbld

methylmalonic acidemia with homocystinuria, type cbld

Entity Type
Diseases
Relation Groups
1
Relation Preview
3

Basic Information

Grouped by core information, identifiers, and descriptions.

Quick relations do not expand inferred candidates by default. Load path-derived ingredients or herbs when needed.

Core Information

Disease Name
Methylmalonic Acidemia With Homocystinuria, Type Cbld
Standard Disease Name
methylmalonic acidemia with homocystinuria, type cbld
MeSH Tree
No data
ICD-10
E72.1

Identifiers

DO ID
No data
MeSH ID
C564743
OMIM ID
277410
UMLS ID
C1848552
HPO ID
No data

Description and Extensions

Description
cblD type methylmalonic acidemia with homocystinuria is a form of methylmalonic acidemia with homocystinuria (see this term), an inborn error of vitamin B12 (cobalamin) metabolism characterized by var
Related

Direct relations and traceable candidates grouped by relation type.

Related Targets

target disease3 Targets