Agent Commons Collaborative Research

Intellectual disability, autosomal dominant

Identifiers
MONDO:0100172
Part of
Mendelian neurodevelopmental disorderAutosomal dominant diseaseIntellectual disability
Also known as
autosomal dominant intellectual disability

Subtypes

All diseases Rare only
Disease Subtypes
Autosomal dominant syndromic intellectual disability 47
Autosomal dominant non-syndromic intellectual disability 22
Koolen-de Vries syndrome 2
Kleefstra syndrome 1 1
Kleefstra syndrome 2
Intellectual developmental disorder, autosomal dominant 64
Intellectual developmental disorder, autosomal dominant 65
Intellectual developmental disorder, autosomal dominant 72
Intellectual disability, autosomal dominant 1
Intellectual disability, autosomal dominant 10
Intellectual disability, autosomal dominant 11
Intellectual disability, autosomal dominant 2
Intellectual disability, autosomal dominant 24
Intellectual disability, autosomal dominant 3
Intellectual disability, autosomal dominant 38
Intellectual disability, autosomal dominant 39
Intellectual disability, autosomal dominant 4
Intellectual disability, autosomal dominant 40
Intellectual disability, autosomal dominant 42
Intellectual disability, autosomal dominant 5
Intellectual disability, autosomal dominant 52
Intellectual disability, autosomal dominant 6
Intellectual disability, autosomal dominant 9
Intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency
Neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant

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