Overview
Clinical overview and emergency guidance are pending physician authorship. Graph-derived data (ontology codes, linked conditions, diagnostic biomarkers) is available below.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Ascher's syndrome
Occasional (5-29%)
Oral-facial-digital syndrome
Frequent (30-79%)
Polyglandular autoimmune syndrome, type 2
von Willebrand disorder
Occasional (5-29%)
Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goiter, and primary gonadal insufficiency
Very frequent (80-99%)
Incontinentia pigmenti syndrome
Frequent (30-79%)
Acrocephalopolysyndactyly type II
Facial milia, lobate tongue, lingual and labial frenula syndrome
Frequent (30-79%)
Distal arthrogryposis type 5
Frequent (30-79%)
Aplasia of fibula co-occurrent with complex brachydactyly
Frequent (30-79%)
Rhizomelic dysplasia of Patterson Lowry type
Very frequent (80-99%)
Ring chromosome 8 syndrome
Very frequent (80-99%)
Anophthalmia plus syndrome
Occasional (5-29%)
Cranioosteoarthropathy
Occasional (5-29%)
Distal monosomy 17q
Very frequent (80-99%)
Developmental delay, hypotonia, extremities hypertrophy syndrome
Very frequent (80-99%)
Dislocation of hip and facial dysmorphism syndrome
Frequent (30-79%)
Orofaciodigital syndrome type 1
Frequent (30-79%)
Trisomy 15 mosaicism
Frequent (30-79%)
Distal duplication 18q
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 203556007
- UMLS CUI
- C4759671
- Fully Specified Name
- Deviation of finger (finding)
- Associated Conditions
- 20
- Diagnostic Tests
- 0
This information is for educational purposes only. If you are experiencing symptoms, please consult a healthcare provider for proper evaluation and diagnosis.