← Back to Conditions

Van den Berghe Dequecker syndrome

disorder
SNOMED 733030003CUI C4518553

Overview

Van den Berghe Dequecker 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.

Absent/underdeveloped radius
Very frequent (80-99%)HP:0006501
Hypoplasia of the ulna
Very frequent (80-99%)HP:0003022
Split hand
Very frequent (80-99%)HP:0001171
Foot ectrodactyly
Frequent (30-79%)HP:0001839

Related Conditions

Multiple malformation syndrome with limb defect as major feature(parent)
Congenital absence of finger(parent)
Congenital hypoplasia of ulna(parent)
Split foot(parent)
Hereditary disorder of musculoskeletal system(parent)
Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT
733030003
UMLS CUI
C4518553
Fully Specified Name
Congenital hypoplasia of ulna and split foot syndrome (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
4
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.