Search Ontology:
Human Disease
DOORS syndrome
- Term ID
- DOID:0111627
- Synonyms
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- autosomal recessive deafness-onychodystrophy syndrome
- deafness-onychodystrophy-osteodystrophy-intellectual disability syndrome
- deafness-onychodystrophy-osteodystrophy-intellectual disability-seizures syndrome
- deafness-onychoosteodystrophy-intellectual disability syndrome
- DOOR syndrome
- DOORS
- Definition
- A syndrome characterized by sensorineural deafness, onychodystrophy, osteodystrophy, seizures, and intellectual disability that has_material_basis_in homozygous or compound heterozygous mutation in the TBC1D24 gene on chromosome 16p13.3. (3)
- References
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- GARD:1685
- MESH:C538204
- MIM:220500
- ORDO:79500
- UMLS_CUI:C0795927
- Ontology
- Human Disease ( DOID:0111627 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models