Auriculo-condylar syndrome

disorder

SNOMED 702443003CUI C1865295

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Dysplastic ears

Very frequent (80-99%)HP:0000377

Hypotrophic mandibular condyle

Very frequent (80-99%)HP:0007628

Notched helix

Very frequent (80-99%)HP:0009902

Abnormality of the crus of the ear

Frequent (30-79%)HP:0009895

Absent/small external ear

Frequent (30-79%)HP:0008772

Angle class 3 malocclusion

Frequent (30-79%)HP:0000689

Cleft of palate

Frequent (30-79%)HP:0000175

Deformity of the temporomandibular joint

Frequent (30-79%)HP:0010754

Hypertrophy of cheeks

Frequent (30-79%)HP:0000293

Hypoplastic mandible

Frequent (30-79%)HP:0000347

Inadequate arch length for tooth size

Frequent (30-79%)HP:0000678

Laboured breathing

Frequent (30-79%)HP:0002098

Narrow ear canal

Frequent (30-79%)HP:0000402

Narrow mouth

Frequent (30-79%)HP:0000160

Obstructive sleep apnea

Frequent (30-79%)HP:0002870

Periauricular skin pits

Frequent (30-79%)HP:0100277

Posterior displacement of the tongue

Frequent (30-79%)HP:0000162

Posteriorly angulated ears

Frequent (30-79%)HP:0000358

Question mark ears

Frequent (30-79%)HP:0030022

Skin tag on the posterior cheek

Frequent (30-79%)HP:0000384

Snoring symptoms

Frequent (30-79%)HP:0025267

Tongue muscle weakness

Frequent (30-79%)HP:0000183

Unbalanced face

Frequent (30-79%)HP:0000324

Uvula bifida

Frequent (30-79%)HP:0000193

Big calvaria

Occasional (5-29%)HP:0000256

Decreased size of tongue

Occasional (5-29%)HP:0000171

Eyelid ptosis

Occasional (5-29%)HP:0000508

Failure of development of condylar head of mandible

Occasional (5-29%)HP:0007627

Feeding difficulties

Occasional (5-29%)HP:0011968

Generalised decreased muscle tone

Occasional (5-29%)HP:0001290

Related Conditions

Autosomal dominant hereditary disorder(parent)

Auditory system hereditary disorder(parent)

Congenital malformation of ear(parent)

Hereditary disorder of musculoskeletal system(parent)

Congenital anomaly of mandible(parent)

Developmental hereditary disorder(parent)

Quick Facts

SNOMED CT: 702443003
UMLS CUI: C1865295
Fully Specified Name: Auriculo-condylar syndrome (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.