Autosomal dominant non-syndromic intellectual disability

rare

Autosomal dominant form of non-syndromic intellectual disability.

Identifiers: MONDO:0015802 Orphanet:178469
Part of: Intellectual disability, autosomal dominant Non-syndromic intellectual disability
Also known as: non-syndromic intellectual disability, autosomal dominant

Subtypes

Disease	ID	Genes
Clark-Baraitser syndrome	MONDO:0030914	TRIP12
Intellectual developmental disorder 59	MONDO:0032795	CAMK2G
Intellectual developmental disorder 60 with seizures	MONDO:0032823	AP2M1
Intellectual developmental disorder 61	MONDO:0032485	MED13
Intellectual developmental disorder 62	MONDO:0032919	DLG4
Intellectual developmental disorder, autosomal dominant 53	MONDO:0030919
Intellectual developmental disorder, autosomal dominant 54	MONDO:0030920	CAMK2B
Intellectual developmental disorder, autosomal dominant 63, with macrocephaly	MONDO:0032939	TRIO
Intellectual developmental disorder, autosomal dominant 73	MONDO:0957536	TAF4
Intellectual disability, autosomal dominant 22	MONDO:0012869	ZBTB18
Intellectual disability, autosomal dominant 33	MONDO:0014580	DPP6
Intellectual disability, autosomal dominant 34	MONDO:0014599	CERT1
Intellectual disability, autosomal dominant 41	MONDO:0014842	TBL1XR1
Intellectual disability, autosomal dominant 43	MONDO:0014858	HIVEP2
Intellectual disability, autosomal dominant 46	MONDO:0030911	KCNQ5
Intellectual disability, autosomal dominant 47	MONDO:0030912	STAG1
Intellectual disability, autosomal dominant 50	MONDO:0030916	NAA15
Intellectual disability, autosomal dominant 51	MONDO:0030917	KMT5B
Intellectual disability, autosomal dominant 56	MONDO:0030922	CLTC
Intellectual disability, autosomal dominant 57	MONDO:0054837	TLK2
Intellectual disability, autosomal dominant 58	MONDO:0020847	SET
Neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language	MONDO:0013266	MEF2C

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