Overview
Aplasia of skin is a disorder.
Auto-generated from clinical reference data. Not a substitute for medical advice.
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Aplasia cutis congenita
Very frequent (80-99%)HP:0001057
Aplasia cutis congenita of vertex
Very frequent (80-99%)HP:0004471
Congenital localised absence of skin
Very frequent (80-99%)HP:0007383
Incomplete closure of the vertebral arch
Very frequent (80-99%)HP:0010301
Skull defect
Very frequent (80-99%)HP:0001362
Open skin sore
Frequent (30-79%)HP:0200042
Abnormality of bone mineral density
Occasional (5-29%)HP:0004348
Erythema
Occasional (5-29%)HP:0010783
Facial muscle weakness of muscles innervated by CN VII
Occasional (5-29%)HP:0010628
Increased bleeding time
Occasional (5-29%)HP:0003010
Partial syndactyly
Occasional (5-29%)HP:0006101
Syndactyly of feet
Occasional (5-29%)HP:0001770
Tactile hypersensitivity
Occasional (5-29%)HP:5200061
Related Conditions
Aplasia cutis congenita(child)
Scalp, ear, nipple syndrome(child)
Hall Berg Rudolph syndrome(child)
Agenesis of cilia of eyelid(child)
Agenesis of phalangeal flexion crease(child)
Aplasia of nail unit(child)
Aplasia of palmar crease(child)
Aplasia of sweat gland(child)
Aplasia cutis congenita of trunk(child)
Congenital absence of soft tissue of distal phalanx of finger(child)
Dermatosis(parent)
Quick Facts
- SNOMED CT
- 254237003
- UMLS CUI
- C0282160
- Fully Specified Name
- Aplasia of skin (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 13
Medical Disclaimer
This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.
Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.