Vitamin B12-responsive methylmalonic…

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Vitamin B12-responsive methylmalonic acidemia

ORPHA:28Disease

Also called Adenosylcobalamin deficiency · Vitamin B12-responsive methylmalonic aciduria

What it is

An inborn error of vitamin B12 (cobalamin) metabolism characterized by recurrent ketoacidotic comas or transient vomiting, dehydration, hypotonia and intellectual deficit, which responds to vitamin B12. There are three types: cblA, cblB and cblD-variant 2 (cblDv2).

Key facts

Age of onset
Childhood
Inheritance
Autosomal recessive
Classified as
Disease

Recorded for the broader condition

Prevalence
1-9 / 100 000 (Europe)Methylmalonic acidemia without homocystinuria

Orphanet records these for the broader condition rather than for this specific form. They are a starting point, not a figure for this subtype — subtypes often differ, and some are defined by being rarer than the condition they sit under.

Signs and symptoms

These ranges are how often a sign appears across everyone diagnosed, not a prediction for one person — most people have some of these and not others. Orphanet also records findings that are specifically absent in this disease; those are in the data but not listed here.

Genes reported in subtypes

MMAAMMABMMADHC

Orphanet records these genes on 3 more specific entries under this disorder, not on this entry itself:

A well-studied disease is usually split into subtypes, and the gene is curated on whichever one the evidence belongs to. Open a subtype to see which gene goes with it.

ICD-10 codes

E71.1filed under a broader ICD-10 category — shared with 34 other rare diseases

ICD-10 has no distinct code for most rare diseases, so many are filed under the nearest available one. A shared code identifies the group, not this disease — the ORPHAcode above is what identifies it.

Related health topics

Reached through the ICD-10 categories this disease is filed under, so these describe the broader group rather than this disease specifically.

Cross-references

GARD 12623MONDO 0017214OMIM 251100OMIM 251110OMIM 277410UMLS C0342720

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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