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Human Disease

autosomal dominant intellectual developmental disorder 51

Term ID
DOID:0080232
Synonyms
  • autosomal dominant mental retardation 51
Definition
An autosomal dominant intellectual developmental disorder that has_material_basis_in heterozygous mutation in the KMT5B gene on chromosome 11q13. https://pubmed.ncbi.nlm.nih.gov/28191889/
References
Ontology
Human Disease   ( DOID:0080232 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models