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Aplasia cutis congenita, scalp

DA: 173

Developmental anomaly information

Definition: Aplasia cutis congenita is a rare anomaly presenting with absence of skin. The most common site is the scalp

Developmental anomaly parent: (empty)

Topology: Skin

System: Human body > Skin

Developmental anomaly category: Aplasia

Case records MDB427, MDB504
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 18:24:39 by farideh

Created: 2008-05-09 02:00:00 by phsaw

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