Term Name: otopalatodigital syndrome spectrum disorder
Synonyms: fronto-otopalatodigital osteodysplasia, OPD spectrum disorder, OPSD
Definition: A bone development disease characterized by typical facial anomalies and a generalized bone dysplasia with osteodysplastic changes with skeletal dysplasia developing as varying combinations and degrees of undertubulation of the long bones, cortical irregularity and campomelia. Most but not all subtypes are associated with mutations in FLNA on chromosome Xq28.
Ontology: Human Disease [DOID:0111782]   ( DOID:0111782 )

Relationships
is a type of: bone development disease
has subtype: Frank-Ter Haar syndrome frontometaphyseal dysplasia Melnick-Needles syndrome otopalatodigital syndrome type 1 otopalatodigital syndrome type 2