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Descriptor English: Retinal Dysplasia
Descriptor Spanish: Displasia Retiniana
Descriptor Portuguese: Displasia Retiniana
Descriptor French: Dysplasie rétinienne
Entry term(s): Dysplasia, Retinal
Dysplasias, Retinal
Retinal Dysplasias
Tree number(s): C11.250.666
C11.270.660
C11.768.660
C16.131.384.784
C16.320.290.660
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D015792
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.
Annotation: do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Previous Indexing: Retina/abnormalities (1966-1989)
Retinal Degeneration (1970-1989)
Public MeSH Note: 90
History Note: 90
DeCS ID: 24864
Unique ID: D015792
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1990/01/01
Date of Entry: 1989/05/25
Revision Date: 2001/07/25
Retinal Dysplasia - Preferred
Concept UI M0024192
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.
Preferred term Retinal Dysplasia
Entry term(s) Dysplasia, Retinal
Dysplasias, Retinal
Retinal Dysplasias



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