Search Ontology:
Human Disease
Helsmoortel-Van Der Aa Syndrome
- Term ID
- DOID:0070058
- Synonyms
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- autosomal dominant mental retardation 28
- HVDAS
- MRD28
- Definition
- An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the ADNP gene on chromosome 20q13.13. https://www.ncbi.nlm.nih.gov/pubmed/24531329
- References
- Ontology
- Human Disease ( DOID:0070058 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models