Search Ontology:
Human Disease
autosomal dominant intellectual developmental disorder 39
- Term ID
- DOID:0070069
- Synonyms
-
- autosomal dominant mental retardation 39
- autosomal dominant non-syndromic intellectual disability 39
- MRD39
- Definition
- An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant heterozygous mutation in the MYT1L gene on chromosome 2p25.3. https://www.ncbi.nlm.nih.gov/pubmed/23033978
- References
- Ontology
- Human Disease ( DOID:0070069 )
- is a type of
Show First 5 Terms
Show All Terms
Other Pages
Genes Involved
| Human Gene | Zebrafish Ortholog | OMIM Term | Disease | OMIM Phenotype ID |
|---|---|---|---|---|
| MYT1L | Intellectual developmental disorder, autosomal dominant 39 | autosomal dominant intellectual developmental disorder 39 | 616521 |
1 - 1 of 1
Show
Zebrafish Models
No data available