Search Ontology:
Human Disease
Harel-Yoon syndrome
- Term ID
- DOID:0081395
- Synonyms
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- Ocular anomalies-axonal neuropathy-developmental delay syndrome
- Definition
- A syndrome that is characterized by delayed psychomotor development, intellectual disability, truncal hypotonia, spasticity, and peripheral neuropathy and that has_material_basis_in heterozygous mutation in the ATAD3A gene on chromosome 1p36. https://pubmed.ncbi.nlm.nih.gov/27640307/
- References
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- MIM:617183
- ORDO:496790
- Ontology
- Human Disease ( DOID:0081395 )
- is a type of
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Genes Involved
Zebrafish Models