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Aniridia

DA: 383




Developmental anomaly information

Definition: A congenital abnormality in which there is only a rudimentary iris. This is due to the failure of the optic cup to grow. Aniridia occurs in a hereditary form, usually autosomal dominant.


Synonyms:

  • Absence of iris


Developmental anomaly parent: Anophtalmos

Topology: Human body > Head and neck > Head > Face > Eyes

System: Human body > Nervous system > Sensory organs > Eyes

Developmental anomaly category: Anomaly of underdevelopment or overdevelopment

Case records
Links
Observed in MDB cases
Observed in combinaisons (MDB)
Observed in malformative diseases (MDB)
Associated genes in profile
Associated genes in malformative diseases
Associated chromosomal diseases
Associated signaling pathways
Associated developmental anomalies

Last modified: 2009-01-07 17:16:15 by farideh

Created: 2008-06-10 14:37:02 by jcfournet



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