Familial median cleft of upper and lower lip

disorder

SNOMED 718552009CUI C4305376

Overview

Familial median cleft of upper and lower lip 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 mandible morphology

Very frequent (80-99%)HP:0000277

Abnormal morphology of the midface

Very frequent (80-99%)HP:0000309

Abnormality of orbicularis oris muscle

Very frequent (80-99%)HP:3000010

Cleft lower lip

Very frequent (80-99%)HP:0010281

Cleft of upper lip

Very frequent (80-99%)HP:0000204

Fusion of gums

Very frequent (80-99%)HP:0012292

Gaps between teeth

Very frequent (80-99%)HP:0000699

Irregular teeth

Very frequent (80-99%)HP:0040079

Malformation of the maxilla

Very frequent (80-99%)HP:0000326

Midline cleft lip

Very frequent (80-99%)HP:0000161

Related Conditions

Recessive hereditary disorder (autosomal)(parent)

Digestive system hereditary disorder(parent)

Central cleft lip(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 718552009
UMLS CUI: C4305376
Fully Specified Name: Familial median cleft of upper and lower lip (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.