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Alpha-N-acetylgalactosaminidase deficiency type 3

Disease Export to PDF
Name:
Alpha-N-acetylgalactosaminidase deficiency type 3
Description:
A rare clinically heterogeneous type of NAGA deficiency with developmental, neurologic and psychiatric manifestations presenting at an intermediate age.
ORPHAcode:
79281
Synonyms:
NAGA deficiency type 3
Schindler disease type 3
XREF(s):
Orphanet
ICD-10
OMIM
Analyte(s):
NAGA
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14