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.
Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome
Frontometaphyseal dysplasia
Frequent (30-79%)
Radial aplasia-thrombocytopenia syndrome
Always present (100%)
Zellweger syndrome
Troyer syndrome
Always present (100%)
Greenberg dysplasia
Pena-Shokeir syndrome type I
Ohdo syndrome, Maat-Kievit-Brunner type
Occasional (5-29%)
Craniofacial deafness hand syndrome
Mowat-Wilson syndrome
Frequent (30-79%)
Multiple epiphyseal dysplasia type 4
Occasional (5-29%)
Congenital lipomatous overgrowth, vascular malformation, epidermal nevi, skeletal anomaly syndrome
Frequent (30-79%)
Asparagine-linked glycosylation 9 congenital disorder of glycosylation
Occasional (5-29%)
8q13 microdeletion syndrome
Always present (100%)
Multicentric carpotarsal osteolysis syndrome
ANE syndrome
Frequent (30-79%)
Teebi Shaltout syndrome
Severe feeding difficulties, failure to thrive, microcephaly due to ASXL3 deficiency syndrome
Frequent (30-79%)
Hirschsprung disease and intellectual disability due to del(2)(q22)
Occasional (5-29%)
Quick Facts
- SNOMED CT
- 249757009
- UMLS CUI
- C0241521
- Fully Specified Name
- Ulnar deviation of hand (finding)
- Associated Conditions
- 19
- 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.