Disease #07205 (CONDCAC (nurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline), OMIM:620636)

Official abbreviation	CONDCAC
Name	nurodegeneration, childhood-onset, with cerebellar ataxia and cognitive decline
OMIM ID	620636
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CAPRIN1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2025-12-01 11:46:29 +01:00 (CET)
Date last edited	N/A

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Global Variome shared LOVD