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.
Dubowitz's syndrome
Occasional (5-29%)
Hecht syndrome
Aarskog syndrome
Frequent (30-79%)
4p partial monosomy syndrome
Marfan's syndrome
Occasional (5-29%)
Nievergelt's syndrome
Always present (100%)
Mietens syndrome
Occasional (5-29%)
Mucopolysaccharidosis, MPS-VII
Frequent (30-79%)
Smith-Lemli-Opitz syndrome
Weaver syndrome
5p partial monosomy syndrome
Camptomelic dysplasia
Occasional (5-29%)
Polyglandular autoimmune syndrome, type 2
Zellweger syndrome
Deficiency of beta-glucuronidase
Frequent (30-79%)
CCA - Congenital contractural arachnodactyly
Scapuloperoneal spinal muscular atrophy
Atelosteogenesis type 2
Frequent (30-79%)
Acrocephalopolysyndactyly type II
Marden Walker syndrome
Occasional (5-29%)
Distal monosomy 1p36
Desmosterolosis
Occasional (5-29%)
Distal arthrogryposis type 2B
Wolf Hirschhorn syndrome
Pallister W syndrome
Very frequent (80-99%)
Quick Facts
- SNOMED CT
- 77599005
- UMLS CUI
- C0231791
- Fully Specified Name
- Toeing-in (finding)
- Associated Conditions
- 25
- 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.