Clinical Trials
1
Total Trials
1
Recruiting
0
With Results
Related Conditions
Dysplasia of eye(child)
Simple microphthalmos(child)
Lenz microphthalmia syndrome(child)
Microcephaly, microphthalmia, ectrodactyly of lower limbs and prognathism syndrome(child)
Colobomatous microphthalmia(child)
Nanophthalmia(child)
Microphthalmia with ankyloblepharon and intellectual disability syndrome(child)
Syndromic microphthalmia due to orthodenticle homeobox 2 mutation(child)
Microphthalmia with brain atrophy syndrome(child)
Microphthalmia with linear skin defect syndrome(child)
Macrosomia, microphthalmia, cleft palate syndrome(child)
Frontonasal dysplasia type 3(child)
Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome(child)
Microphthalmia of right eye(child)
Microphthalmia of left eye(child)
Microphthalmos due to branchio-oculo-facial syndrome(child)
Microphthalmos due to Fryns syndrome(child)
Microphthalmos due to Delleman syndrome(child)
Syndromic nanophthalmos due to Kenny-Caffey syndrome(child)
Congenital anomaly of eye(parent)
Quick Facts
- SNOMED CT
- 61142002
- UMLS CUI
- C0026010
- Fully Specified Name
- Microphthalmos (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- Clinical Trials
- 1
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.