Lipodystrophy due to peptidic growth factors deficiency

disorder

SNOMED 724176001CUI C2931279

Overview

Lipodystrophy due to peptidic growth factors 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 the face

Very frequent (80-99%)HP:0000271

Aplasia/Hypoplasia of the skin

Very frequent (80-99%)HP:0008065

Atrophy of fat

Very frequent (80-99%)HP:0100578

Cachexia

Very frequent (80-99%)HP:0004326

Fallen arches

Very frequent (80-99%)HP:0001763

Flexion contractures

Very frequent (80-99%)HP:0001371

Hooked nose

Very frequent (80-99%)HP:0000444

Hypoplastic mandible condyle

Very frequent (80-99%)HP:0000347

Inability to make and keep healthy fat tissue

Very frequent (80-99%)HP:0009125

Keratoderma

Very frequent (80-99%)HP:0000982

Narrow mouth

Very frequent (80-99%)HP:0000160

Pachydermia

Very frequent (80-99%)HP:0001072

Pectus excavatum

Very frequent (80-99%)HP:0000767

Reduced subcutaneous adipose tissue

Very frequent (80-99%)HP:0003758

Stiff joint

Very frequent (80-99%)HP:0001387

Tight skin

Very frequent (80-99%)HP:0100679

Weight loss

Very frequent (80-99%)HP:0001824

Abnormal circulating lipid concentration

Frequent (30-79%)HP:0003119

Abnormal skin colour

Frequent (30-79%)HP:0001000

Abnormality of the arm

Frequent (30-79%)HP:0002817

Abnormality of the chest

Frequent (30-79%)HP:0000765

Abnormality of the hair shaft

Frequent (30-79%)HP:0001595

Abnormality of the lower limb

Frequent (30-79%)HP:0002814

Atherosclerotic cardiovascular disease

Frequent (30-79%)HP:0002621

Decreased bone mineral density Z score

Frequent (30-79%)HP:0004349

Hyperlipoproteinemia

Frequent (30-79%)HP:0010980

Premature graying of the hair

Frequent (30-79%)HP:0002216

Type I diabetes mellitus

Frequent (30-79%)HP:0100651

Related Conditions

Lipodystrophy(parent)

Quick Facts

SNOMED CT: 724176001
UMLS CUI: C2931279
Fully Specified Name: Lipodystrophy due to peptidic growth factors deficiency (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 28

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.