Disease #05825 (CRDHL2 (dystrophy, cone-rod, and hearing loss, type 2 (CRDHL2)), OMIM:618358)

Global Variome shared LOVD

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Official abbreviation	CRDHL2
Name	dystrophy, cone-rod, and hearing loss, type 2 (CRDHL2)
OMIM ID	618358
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CEP250
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-08-29 08:40:44 +02:00 (CEST)
Date last edited	N/A

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