OBO ID: DOID:0080232
Term Name: autosomal dominant intellectual developmental disorder 51 Search Ontology:
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 )
OTHER autosomal dominant intellectual developmental disorder 51 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
KMT5B Intellectual developmental disorder, autosomal dominant 51 617788
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None