You are using an outdated browser. Please upgrade your browser to improve your experience.
ZTTK syndrome
Disease Summary
Associated Targets (1)
Tbio
1
GARD Rare
Uniprot Description An autosomal dominant syndrome characterized by intellectual disability, developmental delay, malformations of the cerebral cortex, epilepsy, vision problems, musculo-skeletal abnormalities, and congenital malformations.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
This disease has been annotated by GARD as a rare disease.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
OMIM:617140
Orphanet:500150
UMLS:C4310696
MONDO:0014936
High level summary of knowledge for a disease, including descriptions and datasource references.