Overview
Thin skin is a finding that may indicate an underlying health condition requiring clinical evaluation.
Associated Conditions
Conditions associated with this symptom based on HPO disease-phenotype annotations.
Hypercortisolism due to nonpituitary tumor
Frequent (30-79%)
Lenz-Majewski hyperostosis syndrome
Osteogenesis imperfecta, dominant perinatal lethal
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome
Ehlers-Danlos syndrome, type 4
Very frequent (80-99%)
Cross syndrome
Very frequent (80-99%)
Ehlers-Danlos syndrome, hydroxylysine-deficient
Ehlers-Danlos syndrome, type 3
Frequent (30-79%)
Xeroderma pigmentosum
Very frequent (80-99%)
Ehlers-Danlos syndrome, type 8
Arthrochalasis multiplex congenita
Very frequent (80-99%)
Cutis laxa-corneal clouding-oligophrenia syndrome
Very frequent (80-99%)
Ehlers-Danlos syndrome, type 5
Very frequent (80-99%)
Marshall-Smith syndrome
Very frequent (80-99%)
Mandibuloacral dysostosis
Very frequent (80-99%)
Pituitary dependent hypercortisolism
Frequent (30-79%)
Osteogenesis imperfecta, perinatal lethal
Focal dermal hypoplasia
Very frequent (80-99%)
Hereditary acrokeratotic poikiloderma of Weary
Very frequent (80-99%)
Acrogeria
Very frequent (80-99%)
Neonatal pseudo-hydrocephalic progeroid syndrome
Frequent (30-79%)
Multiple symmetrical lipomatosis
Frequent (30-79%)
Christ-Siemens-Touraine syndrome
Saldino-Mainzer dysplasia
Always present (100%)
Stuve-Wiedemann dysplasia
Related Symptoms
Quick Facts
- SNOMED CT
- 277797007
- UMLS CUI
- C0423757
- Fully Specified Name
- Thin skin (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.