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DA: 734

Developmental anomaly information

Definition: Cebocephaly is a very rare congenital anomaly combining alobar holoprosencephaly, ocular hypotelorism, and a proboscis-like nose with single nostril situated below incomplete or underdeveloped closely set eyes.

Developmental anomaly parent: (empty)

Topology: Human body > Head and neck > Head > Cranium > Brain

System: Human body > Nervous system > Central nervous system

Developmental anomaly category: Polytopic field defect

Case records MDB68
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: 2008-12-17 15:58:40 by farideh

Created: 2008-10-01 21:17:58 by farideh

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