Search Ontology:
Human Disease
autosomal dominant intellectual developmental disorder 35
- Term ID
- DOID:0070065
- Synonyms
-
- autosomal dominant mental retardation 35
- autosomal dominant non-syndromic intellectual disability 35
- MRD35
- Definition
- An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the PPP2R5D gene on chromosome 6p21.1. https://www.ncbi.nlm.nih.gov/pubmed/25533962
- References
- Ontology
- Human Disease ( DOID:0070065 )
- is a type of
-
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Genes Involved
| Human Gene | Zebrafish Ortholog | OMIM Term | Disease | OMIM Phenotype ID |
|---|---|---|---|---|
| PPP2R5D | Houge-Janssens syndrome 1 | autosomal dominant intellectual developmental disorder 35 | 616355 |
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Zebrafish Models
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