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Asplenia

DA: 256




Developmental anomaly information

Definition: Congenital asplenia is a congenital absence of the spleen, by splenic regression or splenic aplasia (splenic agenesis). Congenital splenic anomalies are usually accompanied by abnormalities in other organ systems, especially cardiac abnormalities, but they may occur in isolation.


Synonyms:

  • Absent spleen


Developmental anomaly parent: (empty)

Topology: Human body > Abdomen > Spleen

System: Spleen

Developmental anomaly category: Aplasia

Case records MDB11, MDB165, MDB247, MDB345, MDB475, MDB483
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

Here is the list of developmental anomalies associated with this developmental anomaly, based on the cases' information :



Last modified: 2009-01-07 19:01:11 by farideh

Created: 2008-05-23 00:00:00 by phsaw



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