Sonoda syndrome

disorder

SNOMED 715987000CUI C0796162

Overview

Sonoda 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.

Abnormal dermatoglyphics

Very frequent (80-99%)HP:0007477

Abnormal oral cavity morphology

Very frequent (80-99%)HP:0000163

Abnormality of cardiovascular system morphology

Very frequent (80-99%)HP:0030680

Decreased body height

Very frequent (80-99%)HP:0004322

Generalised hyperpigmentation

Very frequent (80-99%)HP:0007440

Hypopigmentation of hair

Very frequent (80-99%)HP:0005599

Narrow mouth

Very frequent (80-99%)HP:0000160

Nostrils anteverted

Very frequent (80-99%)HP:0000463

Retruded nasal dorsum

Very frequent (80-99%)HP:0000457

Round, full face

Very frequent (80-99%)HP:0000311

Small nose

Very frequent (80-99%)HP:0003196

Hypospadias

Frequent (30-79%)HP:0000047

Flat nasal bridge

HP:0005280

High axial triradius

HP:0001042

Mental deficiency

HP:0001249

VSD

HP:0001629

Related Conditions

Congenital heart disease(parent)

Multiple malformation syndrome with facial defects as major feature(parent)

Recessive hereditary disorder (autosomal)(parent)

Cardiovascular system hereditary disorder(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 715987000
UMLS CUI: C0796162
Fully Specified Name: Congenital heart defect with round face and developmental delay syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 16

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.