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Severe combined immunodeficiency with hypereosinophilia

disorder
SNOMED 722067005CUI C2700553

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.

Absence of scalp hair
Always present (100%)HP:0002293
Absent circulating B cells
Always present (100%)HP:0030252
Absent circulating T cells
Always present (100%)HP:0025805
Absent eyebrows
Always present (100%)HP:0002223
Absent natural killer cells
Always present (100%)HP:0040219
Agammaglobulinaemia
Always present (100%)HP:0004432
Axillary lymphadenopathy
Always present (100%)HP:0034752
B cell lymphopenia
Always present (100%)HP:0010976
Bacteria in blood culture
Always present (100%)HP:0031864
Cerebrospinal fluid pleocytosis
Always present (100%)HP:0012229
Cervical lymphadenopathy
Always present (100%)HP:0025289
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
Congenital exfoliative erythroderma
Always present (100%)HP:0007381
Decreased anti-CD3/28-induced T-cell proliferation
Always present (100%)HP:0031382
Decreased natural antibody to blood group agents
Always present (100%)HP:0032139
Decreased proportion of CD8-positive T cells
Always present (100%)HP:0005415
Decreased serum IgG
Always present (100%)HP:0004315
Dermatitis
Always present (100%)HP:0000964
Elevated C-reactive protein level
Always present (100%)HP:0011227
Eosinophilic dermatitis
Always present (100%)HP:0032022
Epidermal hyperkeratosis
Always present (100%)HP:0000962
Erythema
Always present (100%)HP:0010783
Failure of development of eyelashes
Always present (100%)HP:0000561
Fragile hair
Always present (100%)HP:0002299
Generalized lymphadenopathy
Always present (100%)HP:0008940
High immunoglobulin E
Always present (100%)HP:0003212
Hypoalbuminaemia
Always present (100%)HP:0003073
Immune deficiency
Always present (100%)HP:0002721
Impaired lymphocyte transformation with phytohemagglutinin
Always present (100%)HP:0003347

Related Conditions

Hereditary eosinophilia(parent)
Autosomal recessive severe combined immunodeficiency disease(parent)
Disorder of eosinophil(parent)
Inflammatory disorder(parent)

Quick Facts

SNOMED CT
722067005
UMLS CUI
C2700553
Fully Specified Name
Omenn syndrome (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
30
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.