← Back to Conditions

Thalidomide embryopathy syndrome

disorder
SNOMED 36193003CUI C0432365

Overview

Thalidomide embryopathy syndrome 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.

Abnormal fibula morphology
Frequent (30-79%)HP:0002991
Abnormality of cardiovascular system morphology
Frequent (30-79%)HP:0030680
Absent/small thighbone
Frequent (30-79%)HP:0005613
Aplasia/hypoplasia of the humerus
Frequent (30-79%)HP:0006507
Aplastic/hypoplastic thumbs
Frequent (30-79%)HP:0009601
Decreased body height
Frequent (30-79%)HP:0004322
Dysplastic radii
Frequent (30-79%)HP:0006433
Hypoplasia or unilateral/bilateral absence of ulna
Frequent (30-79%)HP:0006495
Preaxial hand polydactyly
Frequent (30-79%)HP:0001177
Split hand
Frequent (30-79%)HP:0001171
Triphalangy of thumb
Frequent (30-79%)HP:0001199
Upper limb phocomelia
Frequent (30-79%)HP:0009813
Absent ears
Occasional (5-29%)HP:0009892
Body fails to respond to insulin
Occasional (5-29%)HP:0000855
Chronic rhinitis
Occasional (5-29%)HP:0002257
Ear anomalies
Occasional (5-29%)HP:0000356
Hypoacusis
Occasional (5-29%)HP:0000365

Quick Facts

SNOMED CT
36193003
UMLS CUI
C0432365
Fully Specified Name
Thalidomide embryopathy syndrome (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
17
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.