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Fetal methyl mercury syndrome

disorder
SNOMED 62110005CUI C0265376

Overview

Fetal methyl mercury syndrome is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

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

Central hypotonia
Very frequent (80-99%)HP:0001252
Deafness
Very frequent (80-99%)HP:0000365
Decreased body height
Very frequent (80-99%)HP:0004322
Decreased size of cranium
Very frequent (80-99%)HP:0000252
Impaired vision
Very frequent (80-99%)HP:0000505

Quick Facts

SNOMED CT
62110005
UMLS CUI
C0265376
Fully Specified Name
Fetal methyl mercury syndrome (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
5
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.