Hypertelorism Teebi type

disorder

SNOMED 724284005CUI C0796179

Overview

Hypertelorism Teebi type 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.

Decreased volume of upper lip

Always present (100%)HP:0000219

Decreased volume of lip vermillion

Very frequent (80-99%)HP:0000233

Disproportionately small hands

Very frequent (80-99%)HP:0200055

Increased distance between eyes

Very frequent (80-99%)HP:0000316

Increased length of philtrum

Very frequent (80-99%)HP:0000343

Prominent nasal root

Very frequent (80-99%)HP:0000426

Thick eyebrow

Very frequent (80-99%)HP:0000574

Thick, flared eyebrows

Very frequent (80-99%)HP:0002553

2 vessel cord

Frequent (30-79%)HP:0001195

ASD

Frequent (30-79%)HP:0000729

Bilateral fifth digit clinodactyly

Frequent (30-79%)HP:0004209

Bilateral ptosis

Frequent (30-79%)HP:0001488

Brachydactyly

Frequent (30-79%)HP:0001156

Broad flat nasal bridge

Frequent (30-79%)HP:0000431

Craniosynostosis of coronal suture

Frequent (30-79%)HP:0004440

Cryptorchidism

Frequent (30-79%)HP:0000028

Decreased projection of lower jaw

Frequent (30-79%)HP:0000347

Down-slanting palpebral fissure

Frequent (30-79%)HP:0000494

Enlarged aortic root

Frequent (30-79%)HP:0002616

Excessive, persistent worry and fear

Frequent (30-79%)HP:0000739

Eyelid ptosis

Frequent (30-79%)HP:0000508

Frontal protuberance

Frequent (30-79%)HP:0002007

Hairline point

Frequent (30-79%)HP:0000349

Heart shaped uterus

Frequent (30-79%)HP:0000813

Helix abnormal

Frequent (30-79%)HP:0011039

Hydrocele testis

Frequent (30-79%)HP:0000034

Hypopigmented macule

Frequent (30-79%)HP:0020073

Inadequate arch length for tooth size

Frequent (30-79%)HP:0000678

Low-set ears

Frequent (30-79%)HP:0000369

Mental and motor retardation

Frequent (30-79%)HP:0001263

Related Conditions

Autosomal dominant hereditary disorder(parent)

Frontonasal dysplasia sequence(parent)

Sphenoidal dysostosis(parent)

Hereditary disorder of musculoskeletal system(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 724284005
UMLS CUI: C0796179
Fully Specified Name: Hypertelorism Teebi type (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 30

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.