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Interfrontal craniofaciosynostosis

disorder
SNOMED 109409003CUI C0432122

Overview

Interfrontal craniofaciosynostosis 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.

Broad flat nasal bridge
Always present (100%)HP:0000431
Delayed language development
Always present (100%)HP:0000750
Increased length of philtrum
Always present (100%)HP:0000343
Metopic synostosis
Always present (100%)HP:0011330
Mongoloid slant
Always present (100%)HP:0000582
Narrow, high-arched roof of mouth
Always present (100%)HP:0002705
Ocular hypotelorism
Always present (100%)HP:0000601
Palpebronasal fold
Always present (100%)HP:0000286
Small nose
Always present (100%)HP:0003196
Triangular head shape
Always present (100%)HP:0000243
Craniosyostosis
HP:0001363
Decreased size of cranium
HP:0000252
Dull intelligence
Excluded (<1%)HP:0001249
Long penis
HP:0000040
Lumbar hemivertebrae
HP:0008439
Meckel diverticulum
HP:0002245
Omphalocoele
HP:0001539
Skin tag on the posterior cheek
HP:0000384
Unibrow
HP:0000664

Quick Facts

SNOMED CT
109409003
UMLS CUI
C0432122
Fully Specified Name
Interfrontal craniofaciosynostosis (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
19
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.