Palmer Pagon syndrome

disorder

SNOMED 1208346003CUI C2931734

Overview

Palmer Pagon 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.

Abnormality of the chest

Very frequent (80-99%)HP:0000765

Abnormality of the urinary system

Very frequent (80-99%)HP:0000079

Communicating hydrocephalus

Very frequent (80-99%)HP:0001334

Hernia of the abdominal wall

Very frequent (80-99%)HP:0004299

Increased nasal height

Very frequent (80-99%)HP:0003189

Increased nasal width

Very frequent (80-99%)HP:0000445

Palpebronasal fold

Very frequent (80-99%)HP:0000286

Anomalous pulmonary venous return

Frequent (30-79%)HP:0010772

PDA

Frequent (30-79%)HP:0001643

Tetrology of fallot

Frequent (30-79%)HP:0001636

Related Conditions

Congenital umbilical defect(parent)

Congenital hydrocephalus(parent)

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

Genetic disease(parent)

Quick Facts

SNOMED CT: 1208346003
UMLS CUI: C2931734
Fully Specified Name: Congenital hydrocephalus, low insertion of umbilicus syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 10

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.