Schindler disease, type 3 Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Alpha-N-acetylgalactosaminidase (NAGA) deficiency type 3 is a rare clinically heterogeneous type of NAGA deficiency (see this term) with developmental, neurologic and psychiatric manifestations presenting at an intermediate age. (Orphanet Rare Disease Ontology, Orphanet_79281)
External Link http://www.ncbi.nlm.nih.gov/medgen/?term=C1836547
Similar Terms
Downloads & Tools

Genes

1 genes associated with the Schindler disease, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
NAGA N-acetylgalactosaminidase, alpha-