Search Ontology:
Human Disease
Kenny-Caffey syndrome type 1
- Term ID
- DOID:0080722
- Synonyms
-
- Definition
- A Kenny-Caffey syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the TBCE gene, encoding tubulin-specific chaperone E, on chromosome 1q42. https://pubmed.ncbi.nlm.nih.gov/9806825/
- References
-
- GARD:8367
- MIM:244460
- ORDO:93324
- Ontology
- Human Disease ( DOID:0080722 )
- is a type of
-
Other Pages
Genes Involved
Zebrafish Models