alpha-N-acetylgalactosaminidase deficiency type 3

Go to external page http://purl.obolibrary.org/obo/MONDO_0019264


Alpha-N-acetylgalactosaminidase (NAGA) deficiency type 3 is a rare clinically heterogeneous type of NAGA deficiency with developmental, neurologic and psychiatric manifestations presenting at an intermediate age. [ Orphanet:79281 ]

This is just here as a test because I lose it

Term information

database cross reference
  • Orphanet:79281 (MONDO:equivalentTo)
  • UMLS:C1836545 (Orphanet:79281)
  • ICD10:E77.1 (Orphanet:79281)
Subsets

ordo_clinical_subtype

definition

Alpha-N-acetylgalactosaminidase (NAGA) deficiency type 3 is a rare clinically heterogeneous type of NAGA deficiency with developmental, neurologic and psychiatric manifestations presenting at an intermediate age.

exactMatch

http://linkedlifedata.com/resource/umls/id/C1836545

http://www.orpha.net/ORDO/Orphanet_79281

has exact synonym

Schindler disease type 3

NAGA deficiency type 3

id

MONDO:0019264

Term relations