Disease #01332 (CFEOM1;CFEOM3B (fibrosis, extraocular muscles, congenital, type 1), OMIM:135700)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CFEOM1;CFEOM3B
Name	fibrosis, extraocular muscles, congenital, type 1
OMIM ID	135700
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	KIF21A
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2022-12-23 14:57:03 +01:00 (CET)

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