Thiemann's disease

disorder

SNOMED 55166000CUI C0264081

Overview

Thiemann's disease 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.

Anomaly of the epiphyses

Very frequent (80-99%)HP:0005930

Bone infarction

Very frequent (80-99%)HP:0010885

Brachydactyly

Frequent (30-79%)HP:0001156

Limitation of joint mobility

Frequent (30-79%)HP:0001376

Abnormal metaphysis morphology

Occasional (5-29%)HP:0000944

Phalangeal hypoplasia

HP:0009803

Widened phalanges

HP:0006009

Related Conditions

Avascular necrosis of bone of hand(parent)

Familial disease(parent)

Injury of finger(parent)

Joint injury(parent)

Genetic disease(parent)

Abnormality of epiphysis morphology of phalanx of hand(parent)

Abnormality of interphalangeal joint of hand morphology(parent)

Quick Facts

SNOMED CT: 55166000
UMLS CUI: C0264081
Fully Specified Name: Thiemann disease familial form (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 7

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.