Disease #00075

Official abbreviation	SNDI
Name	STRIATONIGRAL DEGENERATION, INFANTILE; SNDI
OMIM ID	271930
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	NUP62
Associated tissues	-
Disease features	-
Remarks	-