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Tetramelic monodactyly

disorder
SNOMED 770945001CUI C1861233

Overview

Tetramelic monodactyly 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.

Oligodactyly
Very frequent (80-99%)HP:0012165
Foot ectrodactyly
HP:0001839
Foot monodactyly
HP:0200054
Hand monodactyly
HP:0004058
Split hand
HP:0001171

Related Conditions

Autosomal dominant hereditary disorder(parent)
Dysostosis(parent)
Hereditary disorder of musculoskeletal system(parent)
Developmental hereditary disorder(parent)
Adactyly(parent)
Congenital dysplasia of limb(parent)
Aplasia of limb(parent)
Abnormality of limb bone morphology(parent)

Quick Facts

SNOMED CT
770945001
UMLS CUI
C1861233
Fully Specified Name
Tetramelic monodactyly (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
5
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.