Overview
Ectrodactyly 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
Frequent (30-79%)HP:0001839
Hand monodactyly
Frequent (30-79%)HP:0004058
Partial syndactyly
Frequent (30-79%)HP:0006101
Absent hand
Occasional (5-29%)HP:0004050
Aniridia
Occasional (5-29%)HP:0000526
Sensorineural deafness
Occasional (5-29%)HP:0000407
Split hand
Occasional (5-29%)HP:0001171
Related Conditions
Ectrodactyly-ectodermal dysplasia-clefting syndrome(child)
Split foot(child)
Congenital cleft hand(child)
Tibial aplasia and ectrodactyly syndrome(child)
Microcephaly, microphthalmia, ectrodactyly of lower limbs and prognathism syndrome(child)
Bifid femur co-occurrent with monodactylous ectrodactyly(child)
Acro-dermato-ungual-lacrimal-tooth syndrome(child)
Ectodermal dysplasia with ectrodactyly and macular dystrophy syndrome(child)
Fibular aplasia and ectrodactyly syndrome(child)
Jancar syndrome(child)
Hartsfield syndrome(child)
Ectrodactyly polydactyly syndrome(child)
Adactyly(parent)
Quick Facts
- SNOMED CT
- 81208006
- UMLS CUI
- C0265554
- Fully Specified Name
- Ectrodactyly (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 8
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.