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Solitary median maxillary central incisor syndrome
disorderSNOMED 707609006CUI C1840235
Overview
Solitary median maxillary central incisor 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.
Prominent central palatal ridge
Always present (100%)HP:0002708
Single median incisor
Always present (100%)HP:0006315
Choanal atresia
Frequent (30-79%)HP:0000453
Decreased body height
Frequent (30-79%)HP:0004322
Decreased response to growth hormone stimulation test
Frequent (30-79%)HP:0000824
Decreased size of cranium
Frequent (30-79%)HP:0000252
Midnasal atresia or stenosis
Frequent (30-79%)HP:0010644
Ocular hypotelorism
Frequent (30-79%)HP:0000601
Single brain ventricle
Frequent (30-79%)HP:0001360
Specific learning disability
Frequent (30-79%)HP:0001328
Abnormality of chromosome segregation
Occasional (5-29%)HP:0002916
Abnormality of the nasopharynx
Occasional (5-29%)HP:0001739
Absence of eyeballs
Occasional (5-29%)HP:0000528
Anterior hypopituitarism
Occasional (5-29%)HP:0000830
Cleft of upper lip
Occasional (5-29%)HP:0000204
Cyclopia
Occasional (5-29%)HP:0009914
Decreased size of eyeball
Occasional (5-29%)HP:0000568
Lost smell
Occasional (5-29%)HP:0000458
Mental retardation, mild
Occasional (5-29%)HP:0001256
Notched pupil
Occasional (5-29%)HP:0000589
Prominent midpalatal ridge
HP:0100789
Pyriform aperture stenosis
HP:0025011
Quick Facts
- SNOMED CT
- 707609006
- UMLS CUI
- C1840235
- Fully Specified Name
- Solitary median maxillary central incisor syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 22
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.