Disease #06951 (KILQS (Kilquist syndrome), OMIM:619080)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Joanna Walczak-Sztulpa

Official abbreviation	KILQS
Name	Kilquist syndrome
OMIM ID	619080
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SLC12A2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-08-05 13:50:07 +02:00 (CEST)
Date last edited	N/A

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