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CMAMMA - combined malonic and methylmalonic aciduria
disorderSNOMED 702365002CUI C3280314
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Dicarboxylic acidemia
Very frequent (80-99%)HP:0040145
Dicarboxylic aciduria
Very frequent (80-99%)HP:0003215
Methylmalonic acidemia
Very frequent (80-99%)HP:0002912
Methymalonicaciduria
Very frequent (80-99%)HP:0012120
Seizures
Frequent (30-79%)HP:0001250
Acidosis
Occasional (5-29%)HP:0001941
Behavioral symptoms
Occasional (5-29%)HP:0000708
Complex partial seizures
Occasional (5-29%)HP:0002384
Decreased size of cranium
Occasional (5-29%)HP:0000252
Dehydration
Occasional (5-29%)HP:0001944
Dystonic movements
Occasional (5-29%)HP:0001332
Elevated liver enzymes
Occasional (5-29%)HP:0002910
Encephalopathy
Occasional (5-29%)HP:0001298
Generalized clonic seizures
Occasional (5-29%)HP:0011169
Impaired continence
Occasional (5-29%)HP:0031064
Intermittent diarrhea
Occasional (5-29%)HP:0002254
Intermittent migraine headaches
Occasional (5-29%)HP:0002076
Low blood sugar
Occasional (5-29%)HP:0001943
Memory impairment
Occasional (5-29%)HP:0002354
Nasogastric tube feeding
Occasional (5-29%)HP:0040288
Poor weight gain
Occasional (5-29%)HP:0001508
Psychomotor development deficiency
Occasional (5-29%)HP:0001263
Speech difficulties
Occasional (5-29%)HP:0000750
Truncal hypotonia
Occasional (5-29%)HP:0008936
Vomiting
Occasional (5-29%)HP:0002013
Diarrhea
HP:0002014
Ketoacidosis
HP:0001993
Quick Facts
- SNOMED CT
- 702365002
- UMLS CUI
- C3280314
- Fully Specified Name
- Combined malonic and methylmalonic aciduria (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 27
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.