Ostravik Lindemann Solberg syndrome

disorder

SNOMED 783738002CUI C2931046

Overview

Ostravik Lindemann Solberg 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.

Hamartoma of tongue

Very frequent (80-99%)HP:0011802

Narrowing of blood vessel below aortic heart valve

Very frequent (80-99%)HP:0001682

PDA

Very frequent (80-99%)HP:0001643

2-3 finger cutaneous syndactyly

Frequent (30-79%)HP:0001233

Benign neoplasm of the CNS

Frequent (30-79%)HP:0100835

Cryptorchidism

Frequent (30-79%)HP:0000028

Related Conditions

Congenital heart disease(parent)

Polysyndactyly(parent)

Genetic disease(parent)

Multiple malformation syndrome with limb defect as major feature(parent)

Hamartoma of tongue(parent)

Disorder of digestive system specific to fetus OR newborn(parent)

Quick Facts

SNOMED CT: 783738002
UMLS CUI: C2931046
Fully Specified Name: Heart defect, tongue hamartoma, polysyndactyly syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 6

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.