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.
Cockayne syndrome
Frequent (30-79%)
Cutis laxa, autosomal dominant
Very frequent (80-99%)
Deficiency of glycerone-transferase
Frequent (30-79%)
Doose syndrome
Very rare (1-4%)
Elastoderma
Very frequent (80-99%)
Hutchinson-Gilford syndrome
Very frequent (80-99%)
Neonatal pseudo-hydrocephalic progeroid syndrome
Frequent (30-79%)
Multiple symmetrical lipomatosis
Frequent (30-79%)
Stuve-Wiedemann dysplasia
Frequent (30-79%)
Geroderma osteodysplastica
Always present (100%)
Nicolaides-Baraitser syndrome
Frequent (30-79%)
Barber-Say syndrome
Frequent (30-79%)
Microcephaly, microphthalmia, ectrodactyly of lower limbs and prognathism syndrome
Ablepharon macrostomia syndrome
Frequent (30-79%)
Asparagine-linked glycosylation 8 congenital disorder of glycosylation
Occasional (5-29%)
COG5 (component of oligomeric golgi complex 5) congenital disorder of glycosylation
Occasional (5-29%)
Dermatoleukodystrophy
Craniofaciofrontodigital syndrome
Frequent (30-79%)
Progeroid syndrome Petty type
Always present (100%)
Lamin A/C related cardiocutaneous progeria syndrome
Very frequent (80-99%)
Generalized lipodystrophy, progeroid features, severe intellectual disability syndrome
Very frequent (80-99%)
Quick Facts
- SNOMED CT
- 247434009
- UMLS CUI
- C0037301
- Fully Specified Name
- Wrinkled skin (finding)
- Associated Conditions
- 21
- 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.