Sandifer syndrome

disorder

SNOMED 230314007CUI C0338465

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.

Abnormal head movements

Very frequent (80-99%)HP:0002457

Abnormal posturing

Very frequent (80-99%)HP:0002533

Gastro-esophageal reflux

Very frequent (80-99%)HP:0002020

Torticollis

Very frequent (80-99%)HP:0000473

Abnormal involuntary eye movements

Frequent (30-79%)HP:0012547

Epigastrium pain

Frequent (30-79%)HP:0410019

Esophagitis

Frequent (30-79%)HP:0100633

Feeding difficulties

Frequent (30-79%)HP:0011968

Hematemesis

Frequent (30-79%)HP:0002248

Limited neck movement

Frequent (30-79%)HP:0004637

Low number of red blood cells or haemoglobin

Frequent (30-79%)HP:0001903

Stomach hernia

Frequent (30-79%)HP:0002036

Frequent vomiting

Occasional (5-29%)HP:0002572

Related Conditions

Gastroesophageal reflux disease(parent)

Paroxysmal dystonia(parent)

Intermittent torticollis(parent)

Quick Facts

SNOMED CT: 230314007
UMLS CUI: C0338465
Fully Specified Name: Sandifer syndrome (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.