Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Lymphatic obstruction
Very frequent (80-99%)HP:0001004
Atypical scarring
Frequent (30-79%)HP:0000987
Cobblestone-like hyperkeratosis
Frequent (30-79%)HP:0031288
Dependant oedema
Frequent (30-79%)HP:0010741
Lymph node hypoplasia
Frequent (30-79%)HP:0002732
Lymph nodes lack germinal center
Frequent (30-79%)HP:0002849
Predominantly lower limb lymphedema
Frequent (30-79%)HP:0003550
Recurrent bacterial skin infections
Frequent (30-79%)HP:0005406
Skin dimples
Frequent (30-79%)HP:0010781
Skin erosion
Frequent (30-79%)HP:0200041
Skin infections
Frequent (30-79%)HP:0100658
Skin infections, recurrent
Frequent (30-79%)HP:0001581
Angiosarcoma
Occasional (5-29%)HP:0200058
Cleft of palate
Occasional (5-29%)HP:0000175
Facial swelling
Occasional (5-29%)HP:0000282
Fluid around lungs
Occasional (5-29%)HP:0002202
Laryngeal edema
Occasional (5-29%)HP:0012027
Oedema of the dorsum of hands
Occasional (5-29%)HP:0007514
Open skin sore
Occasional (5-29%)HP:0200042
Periorbital edema
Occasional (5-29%)HP:0100539
Peripheral edema
Occasional (5-29%)HP:0012398
Varicose veins
Occasional (5-29%)HP:0002619
Yellow nails
Occasional (5-29%)HP:0011367
Hypoplasia of lymphatic vessels
HP:0003759
Quick Facts
- SNOMED CT
- 400040008
- UMLS CUI
- C1704424
- Fully Specified Name
- Hereditary lymphedema type II (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 24
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.