Subcutaneous panniculitic cutaneous T-cell lymphoma

disorder

SNOMED 404133000CUI C0522624

Overview

Subcutaneous panniculitic cutaneous T-cell lymphoma 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.

Subcutaneous panniculitis-like T-cell lymphoma

Always present (100%)HP:0034403

Erythematous papule

Very frequent (80-99%)HP:0030350

Inflammation of fat tissue

Very frequent (80-99%)HP:0012490

Abnormality of the coagulation cascade

Frequent (30-79%)HP:0003256

Chills

Frequent (30-79%)HP:0025143

Erythematous plaque

Frequent (30-79%)HP:0025474

Hemophagocytosis

Frequent (30-79%)HP:0012156

Hepatosplenomegaly

Frequent (30-79%)HP:0001433

Open skin sore

Frequent (30-79%)HP:0200042

Pyrexia

Frequent (30-79%)HP:0001945

Tiredness

Frequent (30-79%)HP:0012378

Weight loss

Frequent (30-79%)HP:0001824

Autoimmune disorder

Very rare (1-4%)HP:0002960

Facial swelling

Very rare (1-4%)HP:0000282

Large spleen

Very rare (1-4%)HP:0001744

Low number of red blood cells or haemoglobin

Very rare (1-4%)HP:0001903

Pancytopenia

Very rare (1-4%)HP:0001876

Increased serum ferritin level

HP:0003281

Increased triglycerides

HP:0002155

Low fibrinogen level

HP:0011900

Related Conditions

Primary cutaneous T-cell lymphoma(parent)

Mature T-cell AND/OR NK cell neoplasm(parent)

Quick Facts

SNOMED CT: 404133000
UMLS CUI: C0522624
Fully Specified Name: Subcutaneous panniculitic cutaneous T-cell lymphoma (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 20

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.