Lipodystrophia centrifugalis abdominalis infantalis

disorder

SNOMED 238899009CUI C0406605

Overview

Lipodystrophia centrifugalis abdominalis infantalis 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.

Atrophy of fat

Always present (100%)HP:0100578

Reduced subcutaneous adipose tissue

Very frequent (80-99%)HP:0003758

Lack of fatty tissue below the skin

Frequent (30-79%)HP:0007485

Abnormality of the chest

Occasional (5-29%)HP:0000765

Erythema

Occasional (5-29%)HP:0010783

Inflammation of the lymph nodes

Occasional (5-29%)HP:0002840

Inflammatory abnormality of the skin

Occasional (5-29%)HP:0011123

Scaling skin

Occasional (5-29%)HP:0040189

Hair loss

Very rare (1-4%)HP:0001596

Lack of facial subcutaneous fat

Very rare (1-4%)HP:0005320

Related Conditions

Localised lipoatrophy(parent)

Disorder of abdomen(parent)

Disorder of soft tissue of trunk(parent)

Quick Facts

SNOMED CT: 238899009
UMLS CUI: C0406605
Fully Specified Name: Lipodystrophia centrifugalis abdominalis infantalis (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 10

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.