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Descriptor English: Aniridia
Descriptor Spanish: Aniridia
Descriptor aniridia
Scope note: Anomalía congénita en la que sólo hay un iris rudimentario. Se debe a insuficiencia del crecimiento de la copa óptica. La aniridia se da también de forma hereditaria, generalmente de modo autosómico dominante.
Descriptor Portuguese: Aniridia
Descriptor French: Aniridie
Tree number(s): C11.250.060
C11.270.060
C11.941.375.060
C16.131.384.079
C16.320.290.078
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D015783
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.
Annotation: rudimentary iris; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
Allowable Qualifiers: BL sang
CF liquide cérébrospinal
CI induit chimiquement
CL classification
CO complications
DG imagerie diagnostique
DH diétothérapie
DI diagnostic
DT traitement médicamenteux
EC économie
EH ethnologie
EM embryologie
EN enzymologie
EP épidémiologie
ET étiologie
GE génétique
HI histoire
IM immunologie
ME métabolisme
MI microbiologie
MO mortalité
NU soins infirmiers
PA anatomopathologie
PC prévention et contrôle
PP physiopathologie
PS parasitologie
PX psychologie
RH rééducation et réadaptation
RT radiothérapie
SU chirurgie
TH thérapie
UR urine
VE médecine vétérinaire
VI virologie
DeCS ID: 24520
Unique ID: D015783
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: 2013/07/08
Aniridie - Preferred
Concept UI M0024176
Preferred term Aniridie



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