Severe combined immunodeficiency due to CORO1A deficiency

disorder

SNOMED 1229942009CUI C3809383

Overview

Severe combined immunodeficiency due to CORO1A deficiency 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.

Absolute lymphocyte count decrease

Always present (100%)HP:0001888

Childhood attention deficit/hyperactivity disorder

Always present (100%)HP:0007018

Chronic oral thrush

Always present (100%)HP:0009098

Complete or near-complete absence of specific antibody response to tetanus vaccine

Always present (100%)HP:0410295

Complete or near-complete absence of specific antibody response to unconjugated pneumococcus vaccine

Always present (100%)HP:0410300

Gastro-esophageal reflux

Always present (100%)HP:0002020

Immune deficiency

Always present (100%)HP:0002721

Post-vaccination varicella zoster virus infection

Always present (100%)HP:4000166

Recurrent chest infections

Always present (100%)HP:0002783

Recurrent middle ear infection

Always present (100%)HP:0000403

Recurrent URI

Always present (100%)HP:0002788

Psychomotor development deficiency

HP:0001263

Related Conditions

Autosomal recessive severe combined immunodeficiency disease(parent)

T-B+ SCID - T-cell negative B-cell positive severe combined immunodeficiency(parent)

Quick Facts

SNOMED CT: 1229942009
UMLS CUI: C3809383
Fully Specified Name: Severe combined immunodeficiency due to coronin 1A deficiency (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 12

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.