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Embryopathy caused by isotretinoin

disorder
SNOMED 1237226008CUI C2930972

Overview

Embryopathy caused by isotretinoin 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.

Diminished deep tendon reflexes
Very frequent (80-99%)HP:0001315
Ear anomalies
Very frequent (80-99%)HP:0000356
Microtia
Very frequent (80-99%)HP:0008551
Muscular hypotonia
Very frequent (80-99%)HP:0001252
Biparietal narrowing
Frequent (30-79%)HP:0004422
Cleft of palate
Frequent (30-79%)HP:0000175
Cognitive deficits
Frequent (30-79%)HP:0100543
Decreased projection of mandible
Frequent (30-79%)HP:0000347
Flat nasal bridge
Frequent (30-79%)HP:0005280
Hypoplastic toenails
Frequent (30-79%)HP:0001800
Sacral dimple
Occasional (5-29%)HP:0000960
Spina bifida occulta
Occasional (5-29%)HP:0003298

Quick Facts

SNOMED CT
1237226008
UMLS CUI
C2930972
Fully Specified Name
Embryopathy caused by isotretinoin (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
12
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.