Disease #00447 (CATSHLS (CATSHL syndrome), OMIM:610474)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CATSHLS
Name	CATSHL syndrome
OMIM ID	610474
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant, Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	FGFR3
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-07-09 20:13:41 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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