Overview
Aplasia cutis congenita 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 of vertex
Very frequent (80-99%)HP:0004471
Calvarial defect
Very frequent (80-99%)HP:0001362
Congenital localised absence of skin
Very frequent (80-99%)HP:0007383
Congenital scars
Very frequent (80-99%)HP:0001057
Incomplete closure of the vertebral arch
Very frequent (80-99%)HP:0010301
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 palsy
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
Type 1 aplasia cutis(child)
Type 3 aplasia cutis(child)
Adams-Oliver syndrome(child)
Aplasia cutis congenita due to underlying malformation (Type 4)(child)
Aplasia cutis congenita associated with fetus papyraceus (Type 5)(child)
Aplasia cutis congenita in association with epidermolysis bullosa (Type 6)(child)
Aplasia cutis congenita due to teratogenic drug (Type 7)(child)
Aplasia cutis congenita following intra-uterine infection (Type 8)(child)
Aplasia cutis congenita secondary to malformation syndrome (Type 9)(child)
Aplasia cutis in Trisomy 13 syndrome(child)
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn)(child)
Aplasia cutis in Johanson-Blizzard syndrome(child)
Aplasia cutis with myopia syndrome(child)
Aplasia cutis congenita with intestinal lymphangiectasia syndrome(child)
Oculoectodermal syndrome(child)
SCALP syndrome(child)
Didymosis aplasticosebacea(child)
Aplasia cutis congenita of limb(child)
Aplasia of skin(parent)
Congenital anomaly of skin(parent)
Quick Facts
- SNOMED CT
- 35484002
- UMLS CUI
- C0282160
- Fully Specified Name
- Aplasia cutis congenita (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.