Search Ontology:
Human Disease

obsolete MECP2 duplication syndrome

Term ID
DOID:0080713
Synonyms
Definition
A syndrome that has_material_basis_in an extra copy of the MECP2 gene in each cell, occurs almost exclusively in males and that is characterized by delayed development of motor skills such as sitting and walking. (2)
References
Obsolete
true
Secondary ID:
Merged into
syndromic X-linked intellectual disability Lubs type
Ontology
  ( DOID:0080713 )
Relationships
Other Pages
Genes Involved
Zebrafish Models
Citations