Overview
Leucocyte adherence 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.
Abnormality of neutrophil physiology
Very frequent (80-99%)HP:0011990
Impaired neutrophil chemotaxis
Very frequent (80-99%)HP:0040238
Recurrent bacterial infections
Very frequent (80-99%)HP:0002718
Buccal aphthous ulcers
Frequent (30-79%)HP:0011107
Chronic oral thrush
Frequent (30-79%)HP:0009098
Delayed umbilical cord separation
Frequent (30-79%)HP:0032434
Hypoplastic bone marrow
Frequent (30-79%)HP:0005528
Increased total leukocyte count
Frequent (30-79%)HP:0001974
Lymphoid interstitial pneumonia
Frequent (30-79%)HP:0006527
Otitis media
Frequent (30-79%)HP:0000388
Peritonitis
Frequent (30-79%)HP:0002586
Pneumonia
Frequent (30-79%)HP:0002090
Recurrent fungal infections
Frequent (30-79%)HP:0002841
Recurrent staphylococcal infections
Frequent (30-79%)HP:0007499
Red and swollen gums
Frequent (30-79%)HP:0000230
Repeated bladder infections
Frequent (30-79%)HP:0000010
Respiratory infection
Frequent (30-79%)HP:0011947
Skin infections, recurrent
Frequent (30-79%)HP:0001581
Umbilical cord stump infection
Frequent (30-79%)HP:0032435
Autism
Occasional (5-29%)HP:0000717
BCGiosis
Occasional (5-29%)HP:0020087
Bleeding tendency
Occasional (5-29%)HP:0001892
Bone infection
Occasional (5-29%)HP:0002754
Bronchiectasis
Occasional (5-29%)HP:0002110
Cerebral atrophy
Occasional (5-29%)HP:0002059
Coarse face
Occasional (5-29%)HP:0000280
Decreased body height
Occasional (5-29%)HP:0004322
Dental anomalies
Occasional (5-29%)HP:0000164
Dystrophic nails
Occasional (5-29%)HP:0008404
Glomerulonephritis
Occasional (5-29%)HP:0000099
Related Conditions
Leukocyte adhesion deficiency - type 1(child)
Leucocyte adhesion deficiency - type 2(child)
Leukocyte adhesion deficiency type III(child)
Defective phagocytic cell adhesion(parent)
Qualitative abnormality of granulocyte(parent)
Hereditary white blood cell disorder(parent)
Recessive hereditary disorder (autosomal)(parent)
Quick Facts
- SNOMED CT
- 1187233008
- UMLS CUI
- C5550999
- Fully Specified Name
- Leukocyte adhesion deficiency (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.