Deficiency of monoamine oxidase A

disorder

SNOMED 718210003CUI C0796275

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Behavioural disorders

Very frequent (80-99%)HP:0000708

Intellectual impairment

Very frequent (80-99%)HP:0100543

No development of motor milestones

Occasional (5-29%)HP:0001270

Diarrhea

Very rare (1-4%)HP:0002014

Flushing

Very rare (1-4%)HP:0031284

Autism

HP:0000717

Autoagression

HP:0100716

Dull intelligence

HP:0001249

Essential tremor

HP:0030186

Headache

HP:0002315

Impulsivity

HP:0100710

Intolerance to frustration

HP:0000744

physical aggression

HP:0000718

Related Conditions

Inherited metabolic disorder of nervous system(parent)

Deficiency of monoamine oxidase(parent)

X-linked recessive hereditary disease(parent)

Quick Facts

SNOMED CT: 718210003
UMLS CUI: C0796275
Fully Specified Name: Deficiency of monoamine oxidase A (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 13

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.