<< Previous anomaly entry

Go back to the anomaly list

Next anomaly entry >>

Splenomegaly, congenital

DA: 212

Developmental anomaly information

Definition: Fetal splenomegaly may be seen in anemia due to Rh-alloimmunization , myeloproliferative disorders , or intrauterine infection, hematologic diseases, immunological dioorders, and lipidoses


  • Fetal splenomegaly

Developmental anomaly parent: (empty)

Topology: (empty)

System: (empty)

Developmental anomaly category: (empty)

Case records MDB33, MDB37, MDB109, MDB232, MDB295, MDB333, MDB336, MDB393, MDB398, MDB451, MDB463, MDB478, MDB524
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: 2008-08-01 14:51:41 by farideh

Created: 2008-05-14 02:00:00 by phsaw

<< Previous anomaly entry

Next anomaly entry >>