Congenital glaucoma associated with chromosomal abnormalities

Preferred Label : Congenital glaucoma associated with chromosomal abnormalities;

Origin ID

2032397896;

Automatic exact mappings (from CISMeF team)
- Abnormal chromosome [PASCAL descriptor]
- Abnormal chromosome A [PASCAL descriptor]
Currated CISMeF NLP mapping
- CHROMOSOME ABNORMALITY [WHO-ART Included Term]
- CHROMOSOME DISORDER [WHO-ART High Level Term]
- Chromosomal anomalies [MedDRA LLT]
- Chromosomal disorder (disorder) [SNOMED CT concept]
- Chromosome Disorder [NCIt concept]
- Chromosome abnormality [MedDRA LLT]
- Congenital disorder due to abnormality of chromosome number OR structure (disorder) [SNOMED CT concept]
- Cytogenetic Abnormality [NCIt concept]
- Rare chromosomal anomaly [ORDO Disease]
- chromosomal disease, nos [SNOMED Notion]
- chromosome aberrations [MeSH Descriptor]