autosomal dominant non-syndromic intellectual disability
MONDO:0015802Mondo
Findings
No curated finding names autosomal dominant non-syndromic intellectual disability yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Autosomal dominant form of non-syndromic intellectual disability.
Definition from the Mondo Disease Ontology (MONDO:0015802), read 2026-09-29. CC BY 4.0.
Genes
24 genes
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- ASH1LHGNC:19088
- Supportive · Orphanet · Autosomal dominant · 2021
- BRSK2HGNC:11405
- Supportive · Orphanet · Autosomal dominant · 2021
- CACNG2HGNC:1406
- Supportive · Orphanet · Autosomal dominant · 2021
- CAMK2AHGNC:1460
- Supportive · Orphanet · Autosomal dominant · 2021
- CAMK2BHGNC:1461
- Supportive · Orphanet · Autosomal dominant · 2021
- CDH15HGNC:1754
- Supportive · Orphanet · Autosomal dominant · 2021
- CICHGNC:14214
- Supportive · Orphanet · Autosomal dominant · 2021
- CLTCHGNC:2092
- Supportive · Orphanet · Autosomal dominant · 2021
- CSNK2BHGNC:2460
- Supportive · Orphanet · Autosomal dominant · 2021
- DLL1HGNC:2908
- Supportive · Orphanet · Autosomal dominant · 2021
- DOCK8HGNC:19191
- Supportive · Orphanet · Autosomal dominant · 2021
- DYNC1H1HGNC:2961
- Supportive · Orphanet · Autosomal dominant · 2021
- EPB41L1HGNC:3378
- Supportive · Orphanet · Autosomal dominant · 2021
- GRIN1HGNC:4584
- Supportive · Orphanet · Autosomal dominant · 2021
- HGNC:2557HGNC:2557
- Supportive · Orphanet · Autosomal dominant · 2021
- HIVEP2HGNC:4921
- Supportive · Orphanet · Autosomal dominant · 2021
- KCNQ5HGNC:6299
- Supportive · Orphanet · Autosomal dominant · 2021
- KIRREL3HGNC:23204
- Supportive · Orphanet · Autosomal dominant · 2021
- MBD5HGNC:20444
- Supportive · Orphanet · Autosomal dominant · 2021
- RAB11AHGNC:9760
- Supportive · Orphanet · Autosomal dominant · 2021
- SETHGNC:10760
- Supportive · Orphanet · Autosomal dominant · 2021
- TAOK1HGNC:29259
- Supportive · Orphanet · Autosomal dominant · 2021
- TCF4HGNC:11634
- Supportive · Orphanet · Autosomal dominant · 2021
- TRPM3HGNC:17992
- Supportive · Orphanet · Autosomal dominant · 2021
Where it sits
- Narrower terms (25)
- Clark-Baraitser syndrome
- Coffin-Siris syndrome 6
- intellectual developmental disorder 59
- intellectual developmental disorder 60 with seizures
- intellectual developmental disorder 61
- intellectual developmental disorder 62
- intellectual developmental disorder, autosomal dominant 63, with macrocephaly
- intellectual developmental disorder, autosomal dominant 73
- intellectual disability, autosomal dominant 22
- intellectual disability, autosomal dominant 33
- intellectual disability, autosomal dominant 34
- intellectual disability, autosomal dominant 41
- intellectual disability, autosomal dominant 43
- intellectual disability, autosomal dominant 45
- intellectual disability, autosomal dominant 46
- intellectual disability, autosomal dominant 47
Other names
1 name
Resolves to: autosomal dominant non-syndromic intellectual disability
- Also called
- non-syndromic intellectual disability, autosomal dominant