Search Ontology:
Human Disease
autosomal recessive Segawa syndrome
- Term ID
- DOID:0051059
- Synonyms
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- autosomal recessive DOPA-responsive dystonia
- Definition
- A dystonia that is characterized by onset in infancy of dopa-responsive dystonia and that has_material_basis_in homozygous or compound heterozygous mutation in the tyrosine hydroxylase gene (TH) on chromosome 11p15. (2)
- References
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- MIM:605407
- ORDO:101150
- Ontology
- Human Disease ( DOID:0051059 )
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Genes Involved
Zebrafish Models