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Hereditary lymphoedema type I

disorder
SNOMED 399889006CUI C1704423

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.

Hypoplasia of lymphatic vessels
Always present (100%)HP:0003759
Lymphatic obstruction
Very frequent (80-99%)HP:0001004
Abnormal toenail development
Frequent (30-79%)HP:0100797
Ankle swelling
Frequent (30-79%)HP:0001785
Epidermal hyperkeratosis
Frequent (30-79%)HP:0000962
Hydrocele testis
Frequent (30-79%)HP:0000034
Pedal oedema
Frequent (30-79%)HP:0010741
Predominantly lower limb lymphedema
Frequent (30-79%)HP:0003550
Skin infection
Frequent (30-79%)HP:0100658
Varicose veins
Frequent (30-79%)HP:0002619
Venous abnormality
Frequent (30-79%)HP:0002624
Angiosarcoma
Occasional (5-29%)HP:0200058
Behavioral symptoms
Occasional (5-29%)HP:0000708
Lichenification
Occasional (5-29%)HP:0100725
Palpebronasal fold
Occasional (5-29%)HP:0000286
Papilloma
Occasional (5-29%)HP:0012740
Prominent veins
Occasional (5-29%)HP:0001015
Skin cancer (non-melanoma)
Occasional (5-29%)HP:0008069
Specific learning disability
Occasional (5-29%)HP:0001328
Upslanting toenail
Occasional (5-29%)HP:0032344
Urethral stricture
Occasional (5-29%)HP:0012227
Deformity of face
Very rare (1-4%)HP:0001999
Erysipelas
Very rare (1-4%)HP:0001055
Nonimmune hydrops fetalis
Very rare (1-4%)HP:0001790
Hemangiomata
HP:0001028
Hyperkeratosis over edematous areas
HP:0007448

Quick Facts

SNOMED CT
399889006
UMLS CUI
C1704423
Fully Specified Name
Hereditary lymphedema type I (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
26
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.