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Human Disease

autosomal dominant intellectual developmental disorder 40

Term ID
DOID:0070070
Synonyms
  • autosomal dominant mental retardation 40
  • autosomal dominant non-syndromic intellectual disability 40
  • MRD40
Definition
An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant de novo heterozygous mutation in the CHAMP1 gene on chromosome 13q34. https://www.ncbi.nlm.nih.gov/pubmed/25533962
References
Ontology
Human Disease   ( DOID:0070070 )
Relationships
is a type of
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Genes Involved
Zebrafish Models
Citations