The way property values are displayed:
The way concept relations are shown:
The way concept relations are shown:
Aniridia
Hierarchy: | ∟ ∟ ∟ ∟ Aniridia 19 coordinate concepts1 subordinate concept∟ ∟ ∟ ∟ Aniridia 19 coordinate concepts1 subordinate concept∟ ∟ ∟ Aniridia 19 coordinate concepts1 subordinate concept∟ ∟ ∟ Aniridia 19 coordinate concepts1 subordinate concept∟ ∟ ∟ ∟ Aniridia 19 coordinate concepts1 subordinate conceptX |
Broader terms: | |
Narrower terms: | |
Annotation: | rudimentary iris; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
X |
History note: | |
historyNote*: | 90
X |
publicMeSHNote*: | 90
X |
Scope note: | A congenital abnormality in which there is only a rudimentary iris. This is due to the failure of the optic cup to grow. Aniridia also occurs in a hereditary form, usually autosomal dominant.
X |
activeMeSHYear*: | |
dateCreated*: | 1989-05-25X |
dateEstablished*: | 1990-01-01X |
dateRevised*: | 2001-07-25X |
recordAuthorizer*: | sjnX |
recordMaintainer*: | nnsX |
recordOriginator*: | EGCX |
Type: | |
Coordinate terms: | |
URI: | |
Labels and equivalent concepts: | Värikalvopuutos (fi, replaced) XVärikalvon puuttuminen (fi, replaced) Värikalvon puutos (fi, replaced) Aniridi (sv) Irideremi (sv, replaced) Aniridia (la-FI, replaced) |
Share: |
Loading results...