Disease #05967 (PRLTS6 (Perrault syndrome, type 6 (PRLTS6)), OMIM:617565)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	PRLTS6
Name	Perrault syndrome, type 6 (PRLTS6)
OMIM ID	617565
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ERAL1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-08-19 09:05:42 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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