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Otopaladigital syndrome, Type II;

DA: 227

Developmental anomaly information

Definition: OPD2 is an uncommon X-linked condition characterized by dysmorphic facies, a skeletal dysplasia affecting the axial and appendicular skeleton and extraskeletal anomalies including malformations of the brain, heart, genitourinary system, and intestines.


  • OPD2

Developmental anomaly parent: (empty)

Topology: Human body

System: Human body

Developmental anomaly category: Malformation Syndrome (malformative syndrome)

Case records MDB467

Humpath: 13725

OMIM: 304120

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 16:40:27 by farideh

Created: 2008-05-15 02:00:00 by phsaw

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