Search Ontology:
Human Disease

Popov-Chang syndrome

Term ID
DOID:0070709
Synonyms
Definition
An autosomal dominant intellectual developmental disorder characterized by global developmental delay and impaired intellectual development with poor or absent speech that has_material_basis_in heterozygous mutation in the YWHAZ gene on chromosome 8q22. (2)
References
Ontology
Human Disease   ( DOID:0070709 )
Relationships
Other Pages
Genes Involved
Zebrafish Models