|
| General Information | |||
|---|---|---|---|
| Term | Cogan-Reese syndrome | ID (Ontology) | DOID:0060217 (Human Disease) |
| Definition | An eye disease characterized by variable iris atrophy, pigmented and pedunculated nodules located_in iris and attachment of the iris to the cornea (peripheral anterior synechiae) and characterized_by glaucoma. | ||
| Comment | |||
| Links to External Ontologies | |||
| DO.org | |||
| Annotations | |||
| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
|||
|
No relevant statements available
|
|||
|
||||||
sensory system disease |__eye disease |__Cogan-Reese syndrome |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a | eye disease | ||
| Part of | |||
|
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|
|||
| Secondary IDs | |||
|
|
|||
|
External Crossreferences & Linkouts
|
|||
|
GARD:6125 MEDDRA:10059200 NCI:C84644 ORDO:98980 SNOMEDCT_US_2023_03_01:129624009 UMLS_CUI:C1168173 |
|||