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Human Disease

obsolete Kleefstra Syndrome

Term ID
DOID:0070075
Synonyms
Definition
An autosomal dominant non-syndromic intellectual disability that has_material_basis_in an autosomal dominant mutation of EHMT1 on chromosome 9q34.3. https://www.ncbi.nlm.nih.gov/pubmed/16826528
References
Obsolete
true
Secondary ID:
Merged into
Kleefstra syndrome 1
Ontology
  ( DOID:0070075 )
Relationships
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Genes Involved
Zebrafish Models
Citations