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Fatal infantile lactic acidosis with methylmalonic aciduria
1 OMIM reference -
1 associated gene
5 connected diseases
No signs/symptoms info
Disease Type of connection
Burkitt lymphoma
Precursor T-cell acute lymphoblastic leukemia
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria
Neuralgic amyotrophy
Succinyl-CoA:3-ketoacid CoA transferase deficiency
(no synonyms)

Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease

Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -

Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
SUCLG1 P53597611224
No signs/symptoms info available.