Cogan-Reese Syndrome

Preferred Label : Cogan-Reese Syndrome;

NCIt definition : A very rare syndrome characterized by eye abnormalities that lead to vision impairment. These abnormalities include iris atrophy, decreased corneal endothelium, iris nodules, adhesion of the iris to the lens and glaucoma.;

Details

Origin ID

C84644;

UMLS CUI

C1168173;

Automatic exact mappings (from CISMeF team)
- Cogan-Reese syndrome [ICD-11 More detail]
Currated CISMeF NLP mapping
- Cogan Reese disease [Disease (Nov.)]
- Cogan-Reese syndrome [PASCAL descriptor]
- Cogan-Reese syndrome [DO Concept]
- Cogan-Reese syndrome [SNOMED Notion]
- Cogan-Reese syndrome [ORDO Disease]
- Cogan-Reese syndrome [MedDRA LLT]
- Cogan-Reese syndrome (disorder) [SNOMED CT concept]
DO Cross reference
- Cogan-Reese syndrome [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Cogan Reese disease [Disease (Nov.)]
- Cogan-Reese syndrome [ORDO Disease]
- Cogan-Reese syndrome [MedDRA LLT]
- Cogan-Reese syndrome [SNOMED Notion]
- Cogan-Reese syndrome [PASCAL descriptor]
- Cogan-Reese syndrome [DO Concept]
- Cogan-Reese syndrome (disorder) [SNOMED CT concept]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Neonatal Research Network Terminology [NCIt concept]
disease_has_finding
- Rare Lesion [NCIt concept]

Keyword's position in hierarchy(ies) :

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