Overview
Isotretinoin-like syndrome 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.
Microtia
Very frequent (80-99%)HP:0008551
Abnormality of cardiac atrium morphology
Frequent (30-79%)HP:0005120
Abnormality of cardiac ventricle
Frequent (30-79%)HP:0001713
Abnormality of lung veins
Frequent (30-79%)HP:0011718
Abnormality of the aortic arch
Frequent (30-79%)HP:0012303
Abnormality of the posterior fossa
Frequent (30-79%)HP:0000932
Absent/small inner ear
Frequent (30-79%)HP:0008774
Aortic stenosis
Frequent (30-79%)HP:0001650
Atretic auditory canal
Frequent (30-79%)HP:0000413
Bicuspid aortic valve
Frequent (30-79%)HP:0001647
Bilateral nerve deafness
Frequent (30-79%)HP:0008619
Cleft of palate
Frequent (30-79%)HP:0000175
Conotruncal heart defects
Frequent (30-79%)HP:0001710
Decreased projection of lower jaw
Frequent (30-79%)HP:0000347
Decreased size of cranium
Frequent (30-79%)HP:0000252
Feeding difficulties
Frequent (30-79%)HP:0011968
Gastroesophageal reflux disease
Frequent (30-79%)HP:0002020
Global developmental delay, mild
Frequent (30-79%)HP:0011342
Growth delay as children
Frequent (30-79%)HP:0008897
Inguinal hernia
Frequent (30-79%)HP:0000023
Mongoloid slant
Frequent (30-79%)HP:0000582
Nonsyndromal hydrocephalus
Frequent (30-79%)HP:0000238
Nostrils anteverted
Frequent (30-79%)HP:0000463
PDA
Frequent (30-79%)HP:0001643
PLSVC
Frequent (30-79%)HP:0005301
Skin tag on the posterior cheek
Frequent (30-79%)HP:0000384
Small for gestational age infant
Frequent (30-79%)HP:0001511
Anotia
Occasional (5-29%)HP:0009892
Related Conditions
Microtia(parent)
Multiple malformation syndrome with facial defects as major feature(parent)
Congenital anomaly of aortic arch(parent)
Congenital anomaly of central nervous system(parent)
Auditory system hereditary disorder(parent)
Cardiovascular system hereditary disorder(parent)
Hereditary disorder of nervous system(parent)
Developmental hereditary disorder(parent)
Quick Facts
- SNOMED CT
- 722006004
- UMLS CUI
- C0432364
- Fully Specified Name
- Isotretinoin embryopathy-like syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 28
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.