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The way concept relations are shown:
Retinal Dysplasia
Hierarchy: | ∟ ∟ ∟ ∟ Retinal Dysplasia 30 coordinate concepts∟ ∟ ∟ ∟ Retinal Dysplasia 30 coordinate concepts∟ ∟ ∟ Retinal Dysplasia 30 coordinate concepts∟ ∟ ∟ Retinal Dysplasia 30 coordinate concepts∟ ∟ ∟ Retinal Dysplasia 30 coordinate conceptsX |
Broader terms: | ∟ ∟ ∟ ∟ Retinal Dysplasia ∟ ∟ ∟ ∟ Retinal Dysplasia ∟ ∟ ∟ Retinal Dysplasia ∟ ∟ ∟ Retinal Dysplasia ∟ ∟ ∟ Retinal Dysplasia |
Annotation: | do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
X |
History note: | |
historyNote*: | 90
X |
publicMeSHNote*: | 90
X |
Scope note: | Congenital, often bilateral, retinal abnormality characterized by the arrangement of outer nuclear retinal cells in a palisading or radiating pattern surrounding a central ocular space. This disorder is sometimes hereditary.
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: | Verkkokalvon dysplasia (fi) XDisplasia Retiniana (es) δυσπλασία αμφιβληστροειδούς (el) Retinadysplasie (de) retina - dysplazie (cs) |
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