Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Abnormality of the arm
Very frequent (80-99%)HP:0002817
Abnormality of the lower limb
Very frequent (80-99%)HP:0002814
Absent hand
Very frequent (80-99%)HP:0004050
Aplasia of toe
Very frequent (80-99%)HP:0010760
Aplasia/Hypoplasia of the skin
Very frequent (80-99%)HP:0008065
Calvarial defect
Very frequent (80-99%)HP:0001362
Congenital scars
Very frequent (80-99%)HP:0001057
Cutis marmorata
Very frequent (80-99%)HP:0000965
Decreased hair growth
Very frequent (80-99%)HP:0008070
Undergrowth
Very frequent (80-99%)HP:0001508
Abnormal metacarpal morphology
Frequent (30-79%)HP:0005916
Abnormal pulmonary valve morphology
Frequent (30-79%)HP:0001641
Atresia of the pulmonary artery
Frequent (30-79%)HP:0004935
Brachydactyly
Frequent (30-79%)HP:0001156
Decreased size of eyeball
Frequent (30-79%)HP:0000568
Distal phalangeal hypoplasia
Frequent (30-79%)HP:0009882
Lens opacities
Frequent (30-79%)HP:0000518
Nonsyndromal hydrocephalus
Frequent (30-79%)HP:0000238
Partial syndactyly
Frequent (30-79%)HP:0006101
Split hand
Frequent (30-79%)HP:0001171
Squint
Frequent (30-79%)HP:0000486
Talipes
Frequent (30-79%)HP:0001883
Tetrology of fallot
Frequent (30-79%)HP:0001636
Anonychia of fingernails
Occasional (5-29%)HP:0001817
Aplastic/hypoplastic toenails
Occasional (5-29%)HP:0010624
Arteriovenous malformation
Occasional (5-29%)HP:0100026
Bifid skull
Occasional (5-29%)HP:0002084
Cavity within brain
Occasional (5-29%)HP:0002132
Cirrhosis
Occasional (5-29%)HP:0001394
Congenital hepatic fibrosis
Occasional (5-29%)HP:0002612
Related Conditions
Multiple malformation syndrome with limb defect as major feature(parent)
Aplasia cutis congenita(parent)
Disorder of scalp(parent)
Congenital anomaly of head(parent)
Hereditary disorder of the integument(parent)
Congenital anomaly of limb(parent)
Autosomal hereditary disorder(parent)
Disorder of skin of head(parent)
Developmental hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 34748004
- UMLS CUI
- C0265268
- Fully Specified Name
- Adams-Oliver syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 30
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.