Disease #00108

Official abbreviation	ICRD
Name	Infantile cerebellar-retinal degeneration, 614559 (3)??mitochondrial?
OMIM ID	614559
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	ACO2
Associated tissues	-
Disease features	-
Remarks	-