|Dataset||ClinVar Gene-Phenotype Associations|
|Category||disease or phenotype associations|
|Description||Alpha-N-acetylgalactosaminidase (NAGA) deficiency type 2 is a very rare mild adult type of NAGA deficiency (see this term) with the features of angiokeratoma corporis diffusum (see this term) and mild sensory neuropathy. (Orphanet Rare Disease Ontology, Orphanet_79280)|
|Downloads & Tools|
1 genes associated with the Kanzaki disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.